Q-Med AB jobb i Uppsala

Production Scheduler
Location: Uppsala, Sweden (on-site)

Job Description
Do you have a strong ability to maintain structure and work with planning in a dynamic environment? Would you like to be part of the planning function within Supply Chain at Galderma? If so, keep reading. We are looking for a Production Scheduler!



Responsibilities:

* Communicate production schedules to relevant departments to ensure all stakeholders are informed and can act accordingly.
* Ensure short- and long-term supply of strategic components and finished products to avoid production interruptions.
* Release and schedule manufacturing orders in the ERP system M3 to effectively implement the production plan.
* Assign new batch numbers to manufacturing orders to ensure traceability and proper handling of products.
* Participate daily in DOR (Daily Operations Review) and batch follow-up meetings to monitor and adjust the production plan as needed.
* Manage deviations within Supply Chain to identify and resolve any issues arising in the production process.
* Drive change requests to ensure continuous improvement and efficiency within production planning.



Qualifications:

* Education in logistics or equivalent work experience.
* Experience in production and/or material planning.
* Proficiency in Swedish and English at a professional level.
* Experience in the pharmaceutical industry is advantageous.
* Good understanding of LEAN principles is a plus.



What We Offer:
You will work for an organization that embraces diversity and inclusion, believing that better outcomes are achieved by reflecting the perspectives of our diverse customer base.

Galderma's global center for the aesthetics business area is located in Uppsala, encompassing product development, manufacturing, and marketing. Approximately 600 employees work on world-leading products such as Restylane, Azzalure, and Sculptra.

At Galderma in Uppsala, we offer you the opportunity to work in an exciting, international environment where both personal and professional development are encouraged. Our offices are situated along the Fyris River in Uppsala, just a 10-minute bike ride from Uppsala Central Station.



Next Steps:
If you are interested, we welcome your application via the "Apply Now" link by June 18, 2025. Selection and interviews are conducted on an ongoing basis during the application period, and the position may be filled before the final application date.

If your profile is a match, we will invite you for an initial conversation with the recruiter.

The next step is an interview with the hiring manager.

The final step is a panel interview with the team.



Our People Make a Difference
At Galderma, you'll work with people who are like you-and people who are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos create the perfect environment for people to thrive and excel in what they do.

Senior Filling Engineer

Location: Uppsala, Sweden (on-site, viss flexibilitet för distansarbete)



Job Description

Bli en del av Galdermas framgångsrika tillväxtresa - utvecklas i rollen som Senior Sterilization Engineer!



Vi söker en erfaren och engagerad Senior Filling Engineer till vårt team som arbetar med utveckling av nya injicerbara medical device. I denna roll får du ett tekniskt ledaransvar inom fyllning av injicerbara produkter. Du kommer att leda och genomföra aktiviteter kopplade till fyllningsprocesser inom ramen för våra utvecklingsprogram och CMC-planer. Arbetet omfattar bland annat regulatoriskt stöd, arbete med designkontroll, specifikationer samt stöd till formuleringsteamet. Rollen innebär ett nära samarbete med både interna och externa parter och sträcker sig över hela utvecklingskedjan, från processutveckling till överföring och implementering i den operativa organisationen.



Rollen är både tvärfunktionell och projektinriktad. Du samarbetar nära flera interna funktioner och fungerar som specialist i både operativa och strategiska projektmöten. Uppdraget kombinerar teknisk expertis med praktiska och administrativa inslag och kräver därför god kommunikationsförmåga, stark samarbetsvilja och förmåga att arbeta självständigt.



Teamet består i dag av tio engagerade kollegor med fokus på utveckling av nya produkter och produktionsprocesser.. Eftersom det för närvarande inte finns någon annan som arbetar specifikt med fyllning av injicerbara produkter blir du teamets främsta expert inom området. Du förväntas driva utvecklingen framåt på egen hand, men med stöd och expertis från andra delar av organisationen. Vi erbjuder en arbetsmiljö där inkludering, trivsel och samarbete står i fokus.



Ansvarsområden

* Leda och genomföra aktiviteter kopplade till fyllningsprocesser för injicerbara produkter under utveckling, i enlighet med fastställda CMC-planer, projekt och program
* Utveckla robusta och regulatoriskt godkända fyllningsprocesser
* Säkerställa effektiv teknisk överföring av fyllningsprocesser till relevanta delar av organisationen
* Bidra med tekniskt expertstöd i frågor kopplade till inskick till myndigheter, designkontroll, specifikationer och formulering
* Säkerställa att fyllningsaktiviteter följer uppsatt strategi och plan samt sker i enlighet med gällande regulatoriska krav, Galdermas kvalitetssystem och internationella standarder



Kvalifikationer:

* En bakgrund som maskiningenjör, kemiingenjör eller motsvarande relevant utbildning och erfarenhet
* Erfarenhet av att arbeta med fyllning av sterila läkemedel eller medicintekniska produkter (Medical Devices)
* God förståelse för krav på sterila processer och förpackningsintegritet, till exempel för sprutor eller liknande produkter
* Kunskap om produktionsutrustning och tekniska processer kopplade till tillverkning av sterila produkter
* Förmåga att arbeta strukturerat i en reglerad miljö med högt ställda krav på kvalitet och säkerhet



Vi erbjuder

Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.

I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.

Vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Hos oss blir du en viktig del av ett globalt och växande företag. Du hittar oss i moderna lokaler utmed vackra Fyrisån, endast 10 minuters cykelväg från Uppsala Centralstation.



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag, dock senast den 6 juni 2025. Urval och intervjuer görs löpande under ansökningstiden, tjänsten kan komma att tillsättas innan sista ansökningsdatum.

* Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren
* Nästa steg är en intervju med anställande chef samt ytterligare en chef från verksamheten
* Det sista steget i rekryteringsprocessen innebär att vi genomför referenstagningar



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Senior Sterilization Engineer

Location: Uppsala, Sweden (on-site, viss flexibilitet för distansarbete)



Job Description

Bli en del av Galdermas framgångsrika tillväxtresa - utvecklas i rollen som Senior Sterilization Engineer!



Vi söker en erfaren och engagerad Senior Sterilization Engineer till vårt team som arbetar med utveckling av nya injicerbara medical device. I den här rollen får du ett tekniskt ledaransvar inom sterilisering, ett av de mest avgörande områdena för patientsäkerheten. Därför söker vi dig som har djup kunskap och förståelse för steriliseringsprocessers komplexitet och betydelse. Som Senior Sterilization Engineer leder du arbetet med sterilitet och sterilisering av injicerbara produkter under utveckling. Du ansvarar för aktiviteter som sträcker sig genom hela utvecklingskedjan, från att ta fram nya steriliseringsprocesser till teknisk överföring och implementering i organisationen. Arbetet sker i linje med våra CMC- och produktutvecklingsplaner. Du bidrar även i regulatoriska ärenden, tar fram specifikationer och stöttar formuleringsarbetet.



Rollen är både tvärfunktionell och projektinriktad. Du samarbetar nära flera interna funktioner och fungerar som specialist i både operativa och strategiska frågeställningar. Uppdraget kombinerar teknisk expertis med praktiska och administrativa inslag och kräver därför god kommunikationsförmåga, stark samarbetsvilja och förmåga att arbeta självständigt.



Teamet består i dag av tio engagerade kollegor med fokus på utveckling av nya produkter och produktionsprocesser. Eftersom det för närvarande inte finns någon annan som arbetar specifikt med sterilisering blir du teamets främsta expert inom området. Du förväntas driva utvecklingen framåt på egen hand, men med stöd och expertis från andra delar av organisationen. Vi erbjuder en arbetsmiljö där inkludering, trivsel och samarbete står i fokus.



Ansvarsområden

* Leda och genomföra aktiviteter kopplade till sterilitet och steriliseringsprocesser för injicerbara produkter under utveckling, i enlighet med CMC-planer, projekt och program
* Utveckla nya och effektiva steriliseringsprocesser i linje med regulatoriska och kvalitetsmässiga krav
* Säkerställa smidig teknisk överföring av steriliseringsprocesser till relevanta delar av organisationen
* Bidra i regulatoriska inskick, designkontroll, specifikationer och formulering inom ramen för projekt
* Säkerställa att steriliseringsaktiviteter sker i enlighet med strategier, planer samt gällande regulatoriska krav, Galdermas kvalitetssystem, EHS-krav och internationella standarder



Kvalifikationer:

* En mikrobiologisk, maskinteknisk eller annan relevant teknisk eller naturvetenskaplig utbildning
* Djupgående kunskap om steriliseringsprocesser, dess metoder och komplexitet
* Dokumenterad erfarenhet av att arbeta i projektform, gärna i tvärfunktionella team
* Vana vid att verka inom branscher med högt ställda regulatoriska krav
* Erfarenhet av arbete med medicintekniska produkter (Medical Device)



Vi erbjuder

Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.

I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.

Vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Hos oss blir du en viktig del av ett globalt och växande företag. Du hittar oss i moderna lokaler utmed vackra Fyrisån, endast 10 minuters cykelväg från Uppsala Centralstation.



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag, dock senast den 6 juni 2025. Urval och intervjuer görs löpande under ansökningstiden, tjänsten kan komma att tillsättas innan sista ansökningsdatum.

* Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren
* Nästa steg är en intervju med anställande chef samt ytterligare en chef från verksamheten
* Det sista steget i rekryteringsprocessen innebär att vi genomför referenstagningar



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Do you have deep experience in aseptic manufacturing and visual inspection systems? Are you comfortable stepping in as a subject matter expert when complex technical challenges arise? Galderma is now hiring a Senior Process Engineer with a focus on Aseptic Filling & Visual Inspection to support our continued growth and expansion.



About the role



As Senior Process Engineer, you will work as a subject matter expert (SME) in aseptic filling and visual inspection systems for both pre-filled syringes and vials. You'll play a key role in technical projects, equipment qualification, and process development. The role requires both hands-on expertise and strong collaboration across functions such as Production Engineering, Maintenance, Automation, and Quality.

You'll contribute to the evolution of our filling and inspection capabilities by supporting investigations, leading or participating in projects, and ensuring that systems and equipment are compliant, efficient, and fit for purpose.



Key responsibilities include:

* Lead and contribute to engineering projects related to aseptic filling and visual inspection of pre-filled syringes and vials
* Act as technical owner for filling and inspection equipment and associated specifications
* Provide technical input in deviation handling and root cause investigations
* Support design, procurement, and qualification of new or modified systems
* Collaborate across departments to support manufacturing improvements and regulatory compliance



What we're looking for



You have a university degree in engineering or equivalent practical experience and bring 10+ years of experience from pharmaceutical manufacturing environments. Your expertise lies in aseptic filling and visual inspection, with a solid understanding of Grade A cleanroom standards and cGMP compliance.

You're analytical, detail-oriented, and confident in handling technical investigations and process improvements. You collaborate well across teams, communicate clearly, and take initiative when challenges arise. Fluency in English is required. Apart from this we would appreciate if you bring the following:

* Experience with CAPEX projects related to filling or inspection equipment
* Involvement in equipment commissioning and qualification
* Familiarity with Part 11 compliance and automated systems
* Experience working with external equipment suppliers
* Swedish language skills



Why Galderma?



Galderma is in a period of significant growth, investing in new manufacturing capabilities and expanding internal production. That means the work goes beyond maintaining existing systems - there's a strong focus on designing, implementing, and improving new manufacturing lines and equipment.

The engineering work is technically demanding, involving aseptic manufacturing, cleanroom environments, and compliance with pharmaceutical and medical device regulations. It requires a high level of precision and problem-solving ability.

This position offers variety: no two days look the same and the process engineer is called upon when there are complex problems to solve, new equipment to bring in, or processes to improve.

CSV Engineer



Do you enjoy making sure systems work as they should and want to contribute to high-quality, compliant solutions?

At Galderma, we're growing our engineering team in Uppsala and are looking for a Computerized System Validation (CSV) Engineer to support both daily operations and long-term projects. With new systems being implemented and existing ones evolving, you'll have the opportunity to join us at a time of exciting development and change, with the opportunity to contribute from the start. Galderma is the world's largest independent dermatology company, offering a science-based portfolio across aesthetics, skincare, and therapeutic solutions in close collaboration with healthcare professionals.



The role

You'll be part of a collaborative engineering team that works closely with colleagues in automation, commissioning, qualification, and quality. The team ensures that hardware installations, software validation, and data management are all compliant, reliable, and well-documented. As a CSV Engineer, your focus will be on the validation and qualification of computerized systems connected to Facility, Utility, and Manufacturing areas. You'll ensure systems are implemented correctly, perform as intended, and meet the relevant regulatory requirements such as GxP and GAMP5.



In this role, you will:

* Function as the SME (subject matter expert) regarding Computerized System Validation and provide guidance to engineers within the organizaition and project teams.
* Plan, write, and execute validation protocols (IQ, OQ, PQ) for computerized systems
* Review system design and functionality to ensure compliance with regulatory requirements and industry standards.
* Perform hands-on testing of systems and interfaces
* Ensure that all OT systems and processes meet, and can be used as intended, according to the required standards and regulations.



Who are you?

To thrive as a CSV Engineer at Galderma, you're someone who values collaboration and enjoys being part of a team working toward shared goals. You bring a positive mindset, are flexible in how you work, and take a structured approach to tasks. You're naturally curious about how systems operate, especially within Operational Technology (OT), and you like making sure they run smoothly, communicate correctly, and meet all the right standards.



We believe you also bring:

* At least 5 years of experience with Computerized System Validation (CSV), ideally from the pharmaceutical or medical device industry, where quality and compliance are part of everyday life.
* Familiarity with GxP environments and frameworks like GAMP5
* Experience creating and executing Plans, Protocols, Test Scripts and Reports as they relate to Qualification and Validation of assigned Computerized systems associated with Facility, Utility and Manufacturing GxP systems throughout their lifecycle.
* Proficency with all the phases of SDLC (System Development Life Cycle), STLC (system testing life cycl) processes, Validation methologies and Concepts of Qualification Documents/ Protocols.
* Fluency in both Swedish and English



What we offer in return
You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.

As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.



Next steps
We welcome your application via our company website CAREERS | Galderma. Apply as soon as the selection process is ongoing.

* If your profile is a match, we will invite you for a first conversation with the recruiter.
* The next step is an interview with the hiring manager
* The final step is a panel conversation with the extended team



Our people make a difference
At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Job Title: Digital Systems Learning administrator

Location: Uppsala (possibility of hybrid work, min 3 days office)



Job Description

Galderma Uppsala is looking for a Digital Systems Learning administrator who will administrate the training system PATH and the document management system, D2. The role will provide support to the organization both locally and globally for D2 and locally for PATH.

You will be part of the local support team that trains end-users, update or writes relevant documents for both systems. It is a role that will have contacts and cooperation with many colleagues across the organization both locally and globally.

You will join QA Systems, a team of 11 friendly, dedicated and experienced colleagues working with Galderma's quality management system, internal and external inspection and as QA representatives in projects.



Key Tasks

* Administration of the training system, PATH and document management system, D2
* Provide local support (give training, create How to docs, offer problem solving) for both systems
* Activate, train and build a local network of PATH key users that supports the departments
* Provide data from the systems for analysis
* Assist with setting up training matrixes for Uppsala site and assess relevance of current content
* Participates in and in some cases drive activities to improve the systems and the content in the systems
* Support the mapping of current documents, in current document types, templates and owners
* Support the preparation for future data migration into new electronic document management system



Skills & Qualifications

* Preferably 5-7 years of experience in a similar role with working experience from medical device and/or pharmaceutical industries
* Skilled in using digital technology and platforms
* Proficient in Microsoft word and Excel (PPT is a plus)
* Strong team player with the ability to plan and lead work
* Ability to implement a good idea to reality
* Professional proficiency in Swedish and English



What we offer in return

You will be working for an organization that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.

As Galderma's Global Center of Excellence for Aesthetics, we have in Uppsala a unique edge as we have the whole product chain from research and development to production on-site. Here, our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10-minute bike ride from Uppsala Central Station.



Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as possible, as the selection process is ongoing continuously.

* If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
* The next step is an interview with the hiring manager along with two team members
* The final step in the process will be a reference check



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Do you have deep experience in device assembly, packaging and material handling systems and technical project work in a regulated manufacturing setting? Galderma is now hiring a Senior Process Engineer with a focus on Assembly, Packaging & Material handling to support our ongoing investments in production capacity and technology.



About the role



As Senior Process Engineer, you will serve as a subject matter expert (SME) in the areas of device assembly, packaging, and material handling systems. You'll take the lead in technical projects related to packaging equipment and process changes, and play a key role in ensuring that our production lines remain compliant, efficient, and ready to support new products and formats.

The role involves a mix of engineering leadership, hands-on project work, and collaboration across functions such as Automation, Production Engineering, Maintenance, and Quality. You'll contribute to equipment modifications, process adaptations, and troubleshooting activities, always with a strong focus on compliance and operational readiness.



Key responsibilities include:

* Lead and contribute to engineering projects related to device assembly, packaging and material handling systems.
* Act as technical owner for device assembly, packaging and material transfer equipment and associated specifications
* Provide input during technical investigations and support resolution of assembly, packaging and material handling-related deviations
* Support the design, installation, and qualification of new or modified device assembly, packaging and material handling systems
* Collaborate cross-functionally to ensure equipment and processes meet GMP requirements



What we're looking for



You have a university degree in engineering or equivalent practical experience and bring 10+ years of experience from regulated manufacturing environments. Your background includes deep knowledge of assembly processes, packaging, and automated material handling systems. You have hands-on experience supporting equipment and process changes, with a strong understanding of GMP and compliance frameworks.

You're structured, analytical, and comfortable taking a lead role in technical investigations and improvement projects. You work well across departments, communicate clearly, and take initiative when technical challenges arise. Fluency in English is required, Swedish is a plus.

We would also value experience in:

* CAPEX projects related to packaging or material handling
* Equipment commissioning and qualification
* Product transfers or changes in packaging formats
* Collaboration with automation engineers and equipment suppliers



Why Galderma?



Galderma is in a phase of significant growth, with new production lines and technologies being introduced to support both current operations and future demand. This role gives you the opportunity to work in a technically complex, regulated environment where your experience in packaging and assembly will directly impact operational performance and compliance.

You'll be part of a cross-functional engineering team working with projects that range from process optimization to new product introductions. The work is varied, meaningful, and well suited to someone who enjoys applying their technical expertise to real production challenges.

Job Title: Manufacturing Scientist, Injectable Devices

Location: Uppsala, Sweden (Hybrid)



Job description :

We are looking for a new member to the Device injectables team within Manufacturing Science and Technology. The manufacturing scientist is a subject matter expert (SME) responsible for new product implementation (NPI) into a manufacturing facility, and for support of upstream processes during commercial manufacturing.



Key responsibilities:

*

Support new product implementation (NPI) strategy and all aspects of process validation, including process data reviews, investigations, risk management, and change implementation. Write validation documentation and execute process validation under guidance from senior scientists.
*

Serve as a technical SME representing MSAT in Technology Transfer projects.
*

Process owner to support day-to-day operations with a focus on continuous improvements. Identify opportunities for process enhancement, cost reduction, and efficiency gains, proactively driving necessary changes.
*

Lead and participate in investigations into deviations, incidents, and anomalies within the manufacturing process. Conduct in-depth root cause analysis to identify the underlying reasons for deviations and incidents, focusing on process improvement.
*

Collect data from various sources, including quality control reports, production logs, and other relevant documents, to support investigations and continuous process verification (CPV)
*

Write and review technical documentation ensuring compliance with regulatory and quality standards.
*

Coordinate with other experts and collaborate with cross-functional teams, including production, quality assurance, regulatory affairs, and process development, to ensure thorough investigation and timely issue resolution. Assist senior scientists in information gathering to support research studies and claims, and provide input to risk assessments/FMEAs.
*

Prepare detailed investigation reports, conveying findings and recommendations to management and relevant stakeholders





Skills & Qualifications

*

BSc or MSc degree in a relevant engineering field
*

Good familiarity with upstream manufacturing processes in the medical device and/or biopharmaceutical industry
*

1 to 3 years of experience in upstream operations, preferably in a biopharmaceutical/medical device manufacturing environment
*

Strong knowledge of investigative methodologies and root cause analysis techniques
*

Knowledge of regulatory requirements related to investigations and cGMP
*

Sterilization knowledge is meriting





What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.



We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.



Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as possible, as the selection process is ongoing continuously.

*

If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
*

The next step is an interview with the hiring manager
*

The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Job Title: Sr Manufacturing Scientist, Biologics (Drug product)

Location: Uppsala, Sweden (Hybrid)



Job description :

We are looking for a new member to the Biologics team within Manufacturing Science and Technology. The senior manufacturing scientist is a subject matter expert (SME) responsible for new product implementation (NPI) into a manufacturing facility, with a focus on aseptic drug product manufacturing processes.



Key responsibilities:

*

Develop NPI strategy and support all aspects of process validation, including writing process validation documentation, executing process validation, performing process data reviews, investigations, risk management, and change implementation.
*

Serve as a technical subject matter expert (SME) representing MSAT in Technology Transfer projects.
*

Process owner to support day-to-day operations with a focus on continuous improvements. Identify opportunities for process enhancement, cost reduction, and efficiency gains, proactively driving necessary changes.
*

Lead and participate in investigations of deviations, incidents, and anomalies within the manufacturing process. Conduct in-depth root cause analysis to identify the underlying reasons for deviations and incidents, focusing on process improvement. Provide SME assessments in investigations and change controls as required. Prepare detailed investigation reports, conveying findings and recommendations to management and relevant stakeholders.
*

Collect and analyze data from various sources, including quality control reports, production logs, and other relevant documents, to support investigations and continuous process verification (CPV).
*

Develop and lead execution of technical runs/design of experiments (DoE) with data analysis and recommendations.
*

Maintain comprehensive records of investigations, findings, actions taken, and recommendations, ensuring compliance with regulatory and quality standards
*

Write technical manufacturing documentation and dossier sections and provide responses to regulatory authorities as needed.
*

Coordinate and collaborate with cross-functional teams, including production, quality assurance, regulatory affairs, and process development, to ensure thorough investigation and timely issue resolution. Gather information to support research studies and claims, as well as perform risk assessments/FMEAs.



Skills & Qualifications

*

BSc, MSc, or PhD in a relevant scientific or engineering field, such as Chemistry, Biochemistry, Chemical Engineering, or a related discipline
*

Prior manufacturing process experience within the biopharmaceutical industry with a minimum of 6 years of experience in a biopharmaceutical or manufacturing environment
*

Experience in drug substance and/or drug product manufacturing within a GMP environment
*

Previous experience of drug product manufacturing processes including compounding, filtration, aseptic filling (including setting up aseptic process simulation, APS) and visual inspection
*

Experience with regulatory audits and regulatory requirements, risk management (FMEA), investigative methodologies and root cause analysis techniques is highly meriting
*

Proficiency in data collection, analysis, and reporting with excellent communication, documentation, and collaboration skills.



What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.



We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10-minute bike ride from Uppsala Central Station.



Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as possible, as the selection process is ongoing continuously.

*

If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
*

The next step is an interview with the hiring manager
*

The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Job Title: Manufacturing Scientist, Assembly & Packaging

Location: Uppsala, Sweden (Hybrid)



Job description :

We are looking for a new member to the Assembly and Packaging team within Manufacturing Science and Technology. The manufacturing scientist is a subject matter expert (SME) responsible for new product implementation (NPI) into a manufacturing facility, and for support of assembly and packaging processes during commercial manufacturing.



Key responsibilities:

*

Support new product implementation (NPI) strategy and all aspects of process validation, including process data reviews, investigations, risk management, and change implementation. Write validation documentation and execute process validation under guidance from senior scientists.
*

Serve as a technical SME representing MSAT in Technology Transfer projects.
*

Process owner to support day-to-day operations with a focus on continuous improvements. Identify opportunities for process enhancement, cost reduction, and efficiency gains, proactively driving necessary changes.
*

Lead and participate in investigations into deviations, incidents, and anomalies within the manufacturing process. Conduct in-depth root cause analysis to identify the underlying reasons for deviations and incidents, focusing on process improvement.
*

Collect data from various sources, including quality control reports, production logs, and other relevant documents, to support investigations and continuous process verification (CPV)
*

Write and review technical documentation ensuring compliance with regulatory and quality standards.
*

Coordinate with other experts and collaborate with cross-functional teams, including production, quality assurance, regulatory affairs, and process development, to ensure thorough investigation and timely issue resolution. Assist senior scientists in information gathering to support research studies and claims, and provide input to risk assessments/FMEAs.
*

Prepare detailed investigation reports, conveying findings and recommendations to management and relevant stakeholders



Skills & Qualifications

*

BSc or MSc degree in a relevant engineering field
*

Relevant operational experience from the industry
*

Experience of working with the transfer process from development to production/operations, or experience from a similar position.
*

Good familiarity with downstream manufacturing processes in the medical device and/or biopharmaceutical industry
*

1 to 3 years of experience in assembly and packaging operations, preferably in a biopharmaceutical/medical device manufacturing environment
*

Strong knowledge of investigative methodologies and root cause analysis techniques
*

Knowledge of regulatory requirements related to investigations and cGMP
*

Experience in technical writing



What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.



We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.



Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as possible, as the selection process is ongoing continuously.

* If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
* The next step is an interview with the hiring manager
* The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Job Title: Manager MSAT Assembly & Packaging

Location: Uppsala, Sweden (Hybrid)



Job description :

*

In this role, you will manage a team of Assembly & Packaging manufacturing scientists responsible for new product implementation (NPI) into a manufacturing facility and for support of assembly and packaging processes during commercial manufacturing.
*

You and your team will demonstrate a strong process ownership by turning technologies into manufacturing capabilities by applied science and technical investigations, ensuring continuous process improvements through consistent methodology.



Key responsibilities:

You and your team are responsible for:

*

Implementing plans and programs and support policies and practices related to the end-to-end manufacturing processes of NPI projects at all stages, from prototyping to final stage
*

Enabling smooth transition of products from R&D into full production readiness, with team members representing MSAT in Technology Transfer projects and taking full process ownership
*

Ensuring suggested design made by engineering optimizes the production process in terms of process efficiency, cycle time, reliability, and serviceability
*

Process material for commercial production
*

Identifying and implementing assembly and packaging manufacturing processes for existing biologic and device injectable products
*

Process validation (PV), process trending programs, and continuous process verification (CPV) where applicable
*

Supplying technical manufacturing process expertise for appointed areas supporting daily operations, projects, regulatory applications, and audit presentations
*

Owning change controls within appointed area
*

Assessment and implementation of regulatory requirements according to List of Regulatory Requirements (LoRR)



As Manager MSAT T Assembly & Packaging, you will have extensive contact with other departments and external parties, and are expected foster cooperation and partnership to provide integrated solutions to problems. You will guide key stakeholders on processes, systems and tools, and are to develop strong, trusting cross-functional relationships with senior business leaders



Skills & Qualifications

*

BSc or MSc degree in a relevant engineering field and/or working experience in an industrial environment
*

Minimum of 8 years of experience in a biopharmaceutical/medical device or other regulated environment
*

Previous team management experience
*

Hands on experience with manufacturing processes, control strategies and product interactions in the medical device and/or biopharmaceutical industry.
*

Fluent in English and Swedish





What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.



We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10-minute bike ride from Uppsala Central Station.



Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as possible, as the selection process is ongoing continuously.

*

If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
*

The next step is an interview with the hiring manager
*

The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Job Title: Senior Automation Engineer

Location: Uppsala, Sweden (on site)



Job description:

*

You will manage, plan and oversight to deliver implementation of engineering plans and programs associated with operational automation systems and manufacturing lines perform to required safety, and performance standards.
*

Your responsibilities include developing and executing engineering plans, analyzing issues with manufacturing automation systems and trends, to provide reliable solutions to maintains sustaining status of manufacturing lines.
*

You will develop and maintain relationships with stakeholders. The senior engineer also ensures compliance, supports operations, and represents the company in projects and towards suppliers.



Key responsibilities:

*

Troubleshooting & Support: Provide expert troubleshooting and maintenance support for existing automation systems, ensuring maximum uptime and system performance. Program and configure automation systems, PLCs, HMIs, Vision inspection systems and SCADA solutions.
*

SCADA/PLC Programming: Develop, configure, and optimize SCADA systems and PLC programs for new projects, system upgrades, and continuous improvement initiatives.
*

Automation System Design & Implementation: Lead the design, development, and commissioning of SCADA and PLC-based automation systems for pharmaceutical manufacturing operations.
*

Regulatory Compliance: Ensure that automation systems comply with industry standards and regulatory requirements, including GxP, 21 CFR Part 11, and other relevant pharmaceutical industry standards.
*

Continuous Improvement: Collaborate with cross-functional teams to identify opportunities for process improvements, cost reduction, and automation enhancements. Collaborate with vendors to identify innovative technologies and solutions.
*

Project Management: Manage automation-related projects from initial planning through to implementation and handover, ensuring alignment with timelines, budgets, and quality standards. Troubleshoot and resolve issues as they arise during project execution.
*

Documentation & Reporting: Create and maintain detailed technical documentation, including system designs, process flows, functional specifications, and user manuals.
*

Collaboration: Collaborate closely with engineers, operators, and production teams to ensure seamless integration of automation systems within the production environment. Collaborate with cross-functional teams to develop and implement sustainable manufacturing processes and systems.
*

Technical and firsthand automated equipment troubleshooting, repair, and improvements. Lead and provide mentorship in root cause and corrective action (RCCA). Conform with and abides by all regulations, policies, work procedures, instruction, and all safety rules. Assist in regulatory and internal Compliance audits.



Skills & Qualifications

*

Master's / bachelor's degree in electrical, control or electronic engineering
*

Minimum of 8 years' experience in automation
*

Previous experience within GMP and Part 11 or alternatively from a related regulatory industry.
*

Experience with SCADA systems, historian, Siemens, WinCC, iFix, Wonderware, etc.
*

Familiarity with robotics, motion control MES system
*

Experience with configuring and programing vision system and machine learning software.
*

Experience in capital project execution and machinery/system design.
*

Professional level in English





What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.



We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10-minute bike ride from Uppsala Central Station.



Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as possible, as the selection process is ongoing continuously.

*

If your profile is a match, we will invite you for a first conversation with the recruiter.
*

The next step is an interview with the hiring manager
*

The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else.

At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.



Skiftchef - Bulk, DS and Filling

Location: Uppsala, Sweden (on-site)



Job Description

Är du en erfaren ledare med ett starkt fokus på kvalitet och arbetsmiljö? Vi söker en engagerad Skiftchef till vår nya produktionslina till vår nya fabrik!

I rollen kommer du att leda och utveckla ditt team, säkerställa att produktionen följer gällande kvalitetsstandarder och driva förbättringsarbete för att optimera produktionen. Du kommer att vara ansvarig för att nå dagliga produktionsmål, upprätthålla hög säkerhet och kvalitet, samt att samverka med andra produktions- och supportgrupper. Tjänsten är en ledande roll med möjlighet att påverka och bidra till utvecklingen av vårt framtida produktionsarbete.

Initialt kommer du att arbeta i projektfasen innan kommersiell tillverkning påbörjas, vara med och sätta standarder och arbetssätt. I denna roll får du möjlighet att vara med och växa in och bygga upp från grunden!



Ansvarsområden

* Leda produktion för att uppnå uppsatta mål gällande volym, kvalitet och tid.
* Säkerställa att all produktion följer gällande regelverk och GMP-standarder.
* Ansvara för personalplanering, rekrytering, utbildning och lönesättning.
* Utföra arbetsmiljöansvar, inklusive skyddsronder och avvikelser.
* Hantera och rapportera avvikelser inom ansvarsområdet och följa upp produktionsresultat.
* Samverka med andra avdelningar för att optimera produktion och resursfördelning.
* Driva kontinuerligt förbättringsarbete för att öka effektivitet och kvalitet.
* Ansvara för att introducera och utbilda ny personal inom tillverkningen.



Kvalifikationer

* Gymnasieutbildning eller motsvarande, inom relevant område.
* Erfarenhet av att leda team i en produktionsmiljö, gärna inom läkemedel eller tillverkning, eller annan serviceverksamhet.
* Goda erfarenheter från kvalitetsstyrd verksamhet.
* Flytande svenska i tal och skrift samt goda kunskaper i professionell engelska.
* Förmåga att hantera och prioritera flera uppgifter under tidspress.
* Stark kommunikativ förmåga, både muntligt och skriftligt.
* IT-kunskaper inom Microsoft Office.
* Det är meriterande om du har erfarenhet inom kemi eller biologi.



Vi erbjuder

Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.



Som ny chef på Galderma kommer du att delta i våra ledarskapsprogram och reflektera över hur du leder dig själv och andra. Du kommer också att gå med i ett lokalt nätverk av chefer för att diskutera, utbyta perspektiv och få stöd från kollegor.



I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.



På Galderma i Uppsala har vi verksamhet inom produktutveckling och tillverkning inom dermatologi och vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Vi är belägna längs med Fyrisån i Uppsala, 10 minuters cykelfärd från Uppsala Resecentrum.



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag, dock senast 4 maj 2025. Urval och intervjuer görs löpande under ansökningstiden, och tjänsten kan komma att tillsättas innan sista ansökningsdatum.

* Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren.
* Nästa steg är en intervju med anställande chef
* Andra steget är en panelintervju med teamet
* Sista steget är en facklig intervju



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

At Galderma we're unique and we embrace difference.

Whether it's the unique breadth of our integrated offering that covers Aesthetics, Consumer, and Prescription products; or our commitment to recognising and rewarding people for the contribution they make - working here isn't like anywhere else.

At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.



Job Title: Project Managers at Galderma

Location: Uppsala, Sweeden. On Site



Job Description



As a Project Manager, this person will ensure projects run smoothly, meet goals within time, budget, and quality standards, and follow best practices. They will manage project status and financial reporting, mentor junior employees, and lead process improvements while coordinating with team members.



Key Responsibilities

* Implement processes to achieve project management objectives within scope, time, quality, and budget constraints.
* Execute project management best practices and templates, providing ongoing support and solutions.
* Maintain programs and policies, monitoring dependencies across multiple inter-related projects.
* Gather and report consolidated project status and financial information.
* Collaborate with team members to review and audit adherence to methodologies, budgets, and timing.
* Manage large and complex projects independently, often leading process improvements and design initiatives.
* Mentor junior employees, direct their work, and provide technical guidance to line managers and employees.



Skills & Qualifications

* Have served as Project Manager for capital investment projects, with budgetary responsibility.
* Possess experience in Biotech, Pharmaceutical, and Medical Device manufacturing.
* Demonstrated expertise as a Senior Project Manager, with comprehensive experience across the entire project life cycle and various types of capital investment projects.
* Basic knowledge of process design and relevant regulations.
* Proficiency in both English and Swedish is required.
* Advanced education (e.g., Master's degree) in Mechanical or Chemical Engineering, with a background in Biotechnology.





What we offer in return



At Galderma, you will be part of a dedicated team that focuses on projects from multiple perspectives, ensuring a comprehensive approach to achieving our goals. This role offers you the unique opportunity to shape your own future while making a significant impact on the success of Galderma. Galderma is at the forefront of dermatological research and development, constantly pushing the boundaries of science to improve skin health. With a presence in over 100 countries, your work will contribute to solutions that benefit people worldwide. We are committed to your professional development, offering numerous opportunities for learning and advancement. Our team-oriented approach fosters a supportive and inclusive environment where everyone's contributions are valued. Be part of something bigger - join us in making a difference in the world of dermatology. Your journey to a brighter future starts here. Together, we can achieve greatness.



Next Steps



* If your application is successful and your profile is a match, we will invite you for a first virtual conversation with the recruiter.
* The next step is a virtual conversation with the hiring manager
* The final step is a panel conversation with the extended team





Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Job Title: Commissioning, Qualification, & Verification (CQV) Engineer

Location: Uppsala, Sweden





Job description :

*

You will create, plan the execution of activities, execute, report and maintain deliverables as they relate to Verification and Qualification of assigned new and modified Facility, Utility and Manufacturing GxP systems throughout their lifecycle
*

You will execute and review requalification activities as they relate to the assigned applicable area of responsibility



Key responsibilities :

*

Create and execute Plans, Protocols, Test Scripts and Reports as they relate to Verification and Qualification of assigned new and modified Facility, Utility and Manufacturing GxP systems throughout their lifecycle
*

Execute and review requalification activities as they relate to the assigned applicable area of responsibility
*

Provide technical expertise support to cross functional teams in support of day-to-day manufacturing operations and resolution of non-compliances (e.g. Equipment related deviations)
*

Participate in projects and programs to support the activities of the manufacturing organization. Create Verification and Qualification deliverables in support of system GxP lifecycle
*

Support the Verification, Commissioning and Qualification of new and modified manufacturing assets to ensure they meet their design intent and are fit-for-purpose



Skills & Qualifications

*

Bachelor's degree in engineering or equivalent experience/qualification
*

Minimum of 2 years' experience in CQV
*

Experience in a GMP environment
*

Professional level in Swedish and English





What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10-minute bike ride from Uppsala Central Station.



Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as the selection process is ongoing.

*

If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
*

The next step is an interview with the hiring manager
*

The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Instrument- och valideringsspecialist till QC



Galderma är den framväxande ledaren inom dermatologi som ett renodlat företag, verksamt i cirka 90 länder. Vi erbjuder en innovativ, vetenskapsbaserad portfölj av premiumvarumärken och tjänster som täcker hela spektrat av den snabbt växande dermatologimarknaden genom injicerbar estetik, dermatologisk hudvård och terapeutisk dermatologi. Sedan vår grundläggning 1981 har vi ägnat vår uppmärksamhet och passion åt kroppens största organ - huden - genom att möta individuella konsument- och patientbehov med överlägsna resultat i samarbete med vårdpersonal. Eftersom vi förstår att den hud vi lever i formar våra liv, utvecklar vi dermatologi för varje hudhistoria.



På Galderma ger vi aktivt våra team anledning att tro på vår djärva ambition att bli världens ledande dermatologiföretag. Hos oss har du den ultimata möjligheten att få nya och utmanande arbetsupplevelser och skapa en oöverträffad, direkt påverkan.



Jobbeskrivning



Vi söker en Instrument- och valideringsspecialist för att leda arbetet med kvalificering av instrument, utrustning och datoriserade system inom Galderma Uppsalas laboratorier. I denna roll kommer du att, tillsammans med dina kollegor, ansvara för att våra instrument, utrustningar och system är i kvalificerad status och att personalen som utför kvalificeringar har det stöd de behöver för att kunna arbeta på ett effektivt sätt. Vi förväntar oss också att du bidrar till teamets och QCs utveckling genom att vara nytänkande, kreativ och utvecklingsinriktad.



Ansvarsområden

* Utföra arbetsuppgifter i enlighet med delegationer, QC-certifikat och IT-behörigheter.
* Koordinera, planera och leda arbetet med att kvalificera instrument och system, samt utvecklingsprojekt inom området.
* Bidra till utveckling och administration av processer för att säkerställa att instrument, utrustning och system inom QC är i kvalificerad/kalibrerad status och att Galderma Uppsala arbetar i enlighet med branschpraxis och regulatoriska krav.
* Delta i rapportering av processavvikelser och defekter, delta i IT-projekt och representera området i samband med inspektioner.
* Granska och signera kvalitetsdokument inom kompetensområdet, samt utföra åtgärder relaterade till dataintegritet och hantering av mjukvara för att säkerställa QC-efterlevnad med regulatoriska krav.



Kvalifikationer

* Kandidatexamen inom relevant område, eller motsvarande arbetslivserfarenhet.
* Dokumenterad utbildning och erfarenhet av GXP samt medicintekniska produkter och/eller läkemedelsreglering.
* Erfarenhet av GxP-användning av laboratorieanalyssystem och laboratorieverksamhet.
* Dokumenterad erfarenhet av instrument och systemkvalificering i GxP miljö.
* Förmåga att förklara procedurer eller metoder för både interna och externa parter.
* Svenska och engelska, professionell nivå.
* 5-8 års arbetslivserfarenhet.



Egenskaper

* Ha mod att utmana sig själv och kända processer.
* Agera självständigt i både beslutsfattande och informationsinhämtning.
* Tar initiativ till att skapa förbättringar/samarbeten och driva dessa framåt.
* Noggrant och kvalitetsmedvetet arbetssätt.
* Fokus på kunden och leverera mot uppsatta mål.
* Kunna planera och prioritera med hög personlig effektivitet.



Vi erbjuder



Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.

I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.

På Galderma i Uppsala har vi verksamhet inom produktutveckling och tillverkning inom dermatologi och vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Vi är belägna längs med Fyrisån i Uppsala, 10 minuters cykelfärd från Uppsala Resecentrum.



Nästa steg



Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag. Urval och intervjuer görs löpande under ansökningstiden, och tjänsten kan komma att tillsättas innan sista ansökningsdatum.

* Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren.
* Nästa steg är en intervju med anställande chef.
* Sista steget är en panelintervju med teamet.

Job Title: Senior Project Engineer
Location: Uppsala, Sweden (Hybrid)



Job Description
We're looking for an experience senior Project Engineer to join our team. In this role you will manage, plan and provide oversight to deliver the design, procurement, construction and testing of engineering projects (or assigned elements of engineering projects) from start to finish in accordance with company practices.



You will ensure that engineering projects are completed on time, within budget and meet the required quality and EHS standards.



You will be a part of a bigger team supporting all of our projects related to investments and engineering. You will have the opportunity to work in a dynamic environment with the opportunity to make an impact in Galderma and your own work.



Key Responsibilities

*

Preparing, scheduling, coordinating and monitoring of assigned engineering projects or assigned elements of engineering projects (e.g. engineering lead for defined packages or areas of engineering projects).
*

Ensuring compliance with applicable codes, practices, QA/QC policies, performance standards and specifications
*

Interacting with end users and Subject Matter Experts to understand their needs and represent them in the field
*

Performing overall quality control of the work (budget, schedule, plans, assigned team members performance) and reporting regularly on project status.
*

Assigning responsibilities and deliverables to project team members.
*

Cooperating and communicating effectively with the Project Manager (if applicable) and other project members to provide assistance and technical support
*

Reviewing engineering deliverables and initiating appropriate corrective actions to achieve successful outcomes.



Skills & Qualifications

*

Bachelor's Degree in a relevant field or equivalent experience
*

Several experience of work within engineering projects/investment projects
*

Experience in a GMP environment (Pharma or Medical Device)
*

Ability to work with multiple discipline projects
*

Excellent communication skills in both English and Swedish, with the ability to influence and guide stakeholders.



What we offer in return
You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.



We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.



Next steps
We welcome your application via our company website. Apply as soon as possible though no later than the 30th of April 2025. The selection process is ongoing and the role may be filled prior the last application date.

*

If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
*

The next step is a virtual conversation with the hiring manager
*

The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Job Title: People Solution Center Specialist - Payroll
Location: Uppsala, Sweden (on site)



Job description:
We are seeking a highly skilled Swedish Payroll Process Expert to design, document, and optimize the payroll processes within Galderma Sweden. In this role, you will play a pivotal part in developing efficient and compliant payroll processes while defining robust process controls. You will also manage payroll process documentation and ensure alignment with company policies and Swedish regulatory requirements.





Key responsibilities:

Payroll Process Design & Optimization:

*

Develop, design, and implement end-to-end payroll processes aligned with business needs and Swedish compliance requirements.
*

Evaluate and enhance payroll workflows to increase efficiency, accuracy, and scalability.

Process Mapping & Documentation:

*

Create detailed process flow diagrams, step-by-step guides, and update work instructions for payroll processes.
*

Ensure payroll processes are clearly documented and easily accessible to relevant stakeholders.
*

Partner with stakeholders to ensure payroll processes integrate seamlessly with HR, Finance, and IT systems.

Process Controls & Compliance:

*

Establish and implement internal controls to mitigate payroll risks and ensure compliance with Swedish labor laws and tax regulations.
*

Ensure audits and validations are built into processes to detect and correct errors in a timely manner.

Collaboration & Stakeholder Management:

*

Act as the subject matter expert (SME) for Swedish and Nordics payroll processes, providing guidance to internal and external stakeholders.
*

Work closely with HR, Finance, IT, and external vendors to align payroll processes with organizational goals.
*

Facilitate training sessions for relevant teams to ensure a thorough understanding of payroll processes and controls.

System & Technology Integration:

*

Partner with IT teams to align payroll systems with process requirements.
*

Support system implementations or upgrades, ensuring payroll processes are integrated and optimized.





Skills & Qualifications

*

Bachelor's degree in Business Administration, Human Resources, Finance, or a related field.
*

8+ years of experience in Swedish payroll process design, operations, or consulting.
*

In-depth knowledge of Swedish payroll laws, regulations, and compliance requirements (e.g., Swedish Employment Protection Act, tax laws).
*

Experience with payroll from other Nordics countries
*

Experience with payroll systems (e.g., Hogia, Visma, SAP) and process improvement methodologies (e.g., Lean, Six Sigma).
*

Fluency in Swedish and English required



What we offer in return
You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.

As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.

Next steps
We welcome your application via our company website CAREERS | Galderma. Apply as soon as the selection process is ongoing.

*

If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
*

The next step is an interview with the hiring manager
*

The final step is a panel conversation with the extended team

Our people make a difference
At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Instrument- och valideringsspecialist till QC



Galderma är den framväxande ledaren inom dermatologi som ett renodlat företag, verksamt i cirka 90 länder. Vi erbjuder en innovativ, vetenskapsbaserad portfölj av premiumvarumärken och tjänster som täcker hela spektrat av den snabbt växande dermatologimarknaden genom injicerbar estetik, dermatologisk hudvård och terapeutisk dermatologi. Sedan vår grundläggning 1981 har vi ägnat vår uppmärksamhet och passion åt kroppens största organ - huden - genom att möta individuella konsument- och patientbehov med överlägsna resultat i samarbete med vårdpersonal. Eftersom vi förstår att den hud vi lever i formar våra liv, utvecklar vi dermatologi för varje hudhistoria.



På Galderma ger vi aktivt våra team anledning att tro på vår djärva ambition att bli världens ledande dermatologiföretag. Hos oss har du den ultimata möjligheten att få nya och utmanande arbetsupplevelser och skapa en oöverträffad, direkt påverkan.



Jobbeskrivning



Vi söker en Instrument- och valideringsspecialist för att leda arbetet med kvalificering av instrument, utrustning och datoriserade system inom Galderma Uppsalas laboratorier. I denna roll kommer du att, tillsammans med dina kollegor, ansvara för att våra instrument, utrustningar och system är i kvalificerad status och att personalen som utför kvalificeringar har det stöd de behöver för att kunna arbeta på ett effektivt sätt. Vi förväntar oss också att du bidrar till teamets och QCs utveckling genom att vara nytänkande, kreativ och utvecklingsinriktad.



Ansvarsområden

* Utföra arbetsuppgifter i enlighet med delegationer, QC-certifikat och IT-behörigheter.
* Koordinera, planera och leda arbetet med att kvalificera instrument och system, samt utvecklingsprojekt inom området.
* Bidra till utveckling och administration av processer för att säkerställa att instrument, utrustning och system inom QC är i kvalificerad/kalibrerad status och att Galderma Uppsala arbetar i enlighet med branschpraxis och regulatoriska krav.
* Delta i rapportering av processavvikelser och defekter, delta i IT-projekt och representera området i samband med inspektioner.
* Granska och signera kvalitetsdokument inom kompetensområdet, samt utföra åtgärder relaterade till dataintegritet och hantering av mjukvara för att säkerställa QC-efterlevnad med regulatoriska krav.



Kvalifikationer

* Kandidatexamen inom relevant område, eller motsvarande arbetslivserfarenhet.
* Dokumenterad utbildning och erfarenhet av GXP samt medicintekniska produkter och/eller läkemedelsreglering.
* Erfarenhet av GxP-användning av laboratorieanalyssystem och laboratorieverksamhet.
* Dokumenterad erfarenhet av instrument och systemkvalificering i GxP miljö.
* Förmåga att förklara procedurer eller metoder för både interna och externa parter.
* Svenska och engelska, professionell nivå.
* 5-8 års arbetslivserfarenhet.



Egenskaper

* Ha mod att utmana sig själv och kända processer.
* Agera självständigt i både beslutsfattande och informationsinhämtning.
* Tar initiativ till att skapa förbättringar/samarbeten och driva dessa framåt.
* Noggrant och kvalitetsmedvetet arbetssätt.
* Fokus på kunden och leverera mot uppsatta mål.
* Kunna planera och prioritera med hög personlig effektivitet.



Vi erbjuder



Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.

I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.

På Galderma i Uppsala har vi verksamhet inom produktutveckling och tillverkning inom dermatologi och vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Vi är belägna längs med Fyrisån i Uppsala, 10 minuters cykelfärd från Uppsala Resecentrum.



Nästa steg



Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag. Urval och intervjuer görs löpande under ansökningstiden, och tjänsten kan komma att tillsättas innan sista ansökningsdatum.

* Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren.
* Nästa steg är en intervju med anställande chef.
* Sista steget är en panelintervju med teamet.

Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else.



At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.



Operatör (Aseptisk fyllning)

Location: Uppsala (on-site, skiftgång)



Job Description

Nu har du möjlighet att bli en del av Galdermas tillväxtresa och utvecklas i rollen operatör!



Vi söker nu en ny operatör till vår läkemedelstillverkning där du har möjligheten att vara med från början i uppstarten av en ny produktionslina för vår framtida läkemedelsprodukt.



Nuvarande produktionsgrupp på lina 4 består idag av operatörer, labingenjörer samt process- och kvalitetsingenjörer. Tillsammans är ni ansvariga för tillverkning, förvaltning och utveckling av produktionsprocesser för vår biologiska läkemedelsprodukt. Gruppen har en mycket god gemenskap och värdesätter ett arbetsklimat där alla ska trivas.



Ansvarsområden

Rollen är riktad mot den del av linan som ansvarar för formulering (bulk) och aseptisk fyllning. I din tjänst kommer du att:

*

Delta aktivt och ta ansvarar för att tillverkning utförs enligt uppsatta instruktioner och specificerade kvalitetskrav.
*

Delta i den dagliga tillverkningsprocessen samt mediafyllningar
*

Ta ansvar för processer och utrustning inom ditt ansvarsområde
*

Delar med dig av din kunskap till andra för att med stort kundfokus leverera en kvalitetssäkrad produkt till marknaden.



Kvalifikationer:

* Avslutad gymnasieutbildning.
* Flytande svenska, både i tal och skrift.
* Erfarenhet av aseptiskt operatörsarbete
* Kunskap om och erfarenhet av att arbeta med strikta aseptiska processer inom läkemedelsproduktion.
* Förmåga att följa och dokumentera strikt efterlevnad av GMP.



Som operatör inom läkemedelsbranschen är det viktigt att du är noggrann och har ett kvalitetstänk, samt att du har god samarbetsförmåga. Du är behjälplig och kan integrera med teamet där ge och ta feedback är en viktig del i det dagliga arbetet. Rollen kräver att du är driven och lugn, samt tar ansvar för ditt arbete. Du är flexibel och uppskattar den höga pulsen produktionen, samtidigt som du trivs bra med rutinarbete.



Övrigt

I tjänsten kommer skiftarbete att ingå.



Vi erbjuder

Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.



I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.



Vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Hos oss blir du en viktig del av ett globalt och växande företag. Du hittar oss i moderna lokaler utmed vackra Fyrisån, endast 10 minuters cykelväg från Uppsala Centralstation.



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag. Urval och intervjuer görs löpande under ansökningstiden, och tjänsten kan komma att tillsättas innan sista ansökningsdatum.

*

Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren.
*

Nästa steg är en intervju med anställande chef
*

Sista steget är en säkerhetsklassning



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Job Title: Commissioning, Qualification, & Verification (CQV) Engineer

Location: Uppsala, Sweden





Job description :

*

You will create, plan the execution of activities, execute, report and maintain deliverables as they relate to Verification and Qualification of assigned new and modified Facility, Utility and Manufacturing GxP systems throughout their lifecycle
*

You will execute and review requalification activities as they relate to the assigned applicable area of responsibility



Key responsibilities :

*

Create and execute Plans, Protocols, Test Scripts and Reports as they relate to Verification and Qualification of assigned new and modified Facility, Utility and Manufacturing GxP systems throughout their lifecycle
*

Execute and review requalification activities as they relate to the assigned applicable area of responsibility
*

Provide technical expertise support to cross functional teams in support of day-to-day manufacturing operations and resolution of non-compliances (e.g. Equipment related deviations)
*

Participate in projects and programs to support the activities of the manufacturing organization. Create Verification and Qualification deliverables in support of system GxP lifecycle
*

Support the Verification, Commissioning and Qualification of new and modified manufacturing assets to ensure they meet their design intent and are fit-for-purpose



Skills & Qualifications

*

Bachelor's degree in engineering or equivalent experience/qualification
*

Minimum of 2 years' experience in CQV
*

Experience in a GMP environment
*

Professional level in Swedish and English





What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10-minute bike ride from Uppsala Central Station.



Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as the selection process is ongoing.

*

If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
*

The next step is an interview with the hiring manager
*

The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else.



At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.



Skiftchef - Bulk, DS and Filling

Location: Uppsala, Sweden (on-site)



Job Description

Är du en erfaren ledare med ett starkt fokus på kvalitet och arbetsmiljö? Vi söker en engagerad Skiftchef till vår nya produktionslina till vår nya fabrik!

I rollen kommer du att leda och utveckla ditt team, säkerställa att produktionen följer gällande kvalitetsstandarder och driva förbättringsarbete för att optimera produktionen. Du kommer att vara ansvarig för att nå dagliga produktionsmål, upprätthålla hög säkerhet och kvalitet, samt att samverka med andra produktions- och supportgrupper. Tjänsten är en ledande roll med möjlighet att påverka och bidra till utvecklingen av vårt framtida produktionsarbete.

Initialt kommer du att arbeta i projektfasen innan kommersiell tillverkning påbörjas, vara med och sätta standarder och arbetssätt. I denna roll får du möjlighet att vara med och växa in och bygga upp från grunden!



Ansvarsområden

* Leda produktion för att uppnå uppsatta mål gällande volym, kvalitet och tid.
* Säkerställa att all produktion följer gällande regelverk och GMP-standarder.
* Ansvara för personalplanering, rekrytering, utbildning och lönesättning.
* Utföra arbetsmiljöansvar, inklusive skyddsronder och avvikelser.
* Hantera och rapportera avvikelser inom ansvarsområdet och följa upp produktionsresultat.
* Samverka med andra avdelningar för att optimera produktion och resursfördelning.
* Driva kontinuerligt förbättringsarbete för att öka effektivitet och kvalitet.
* Ansvara för att introducera och utbilda ny personal inom tillverkningen.



Kvalifikationer

* Gymnasieutbildning eller motsvarande, inom relevant område.
* Erfarenhet av att leda team i en produktionsmiljö, gärna inom läkemedel eller tillverkning, eller annan serviceverksamhet.
* Goda erfarenheter från kvalitetsstyrd verksamhet.
* Flytande svenska i tal och skrift samt goda kunskaper i professionell engelska.
* Förmåga att hantera och prioritera flera uppgifter under tidspress.
* Stark kommunikativ förmåga, både muntligt och skriftligt.
* IT-kunskaper inom Microsoft Office.
* Det är meriterande om du har erfarenhet inom kemi eller biologi.



Vi erbjuder

Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.



Som ny chef på Galderma kommer du att delta i våra ledarskapsprogram och reflektera över hur du leder dig själv och andra. Du kommer också att gå med i ett lokalt nätverk av chefer för att diskutera, utbyta perspektiv och få stöd från kollegor.



I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.



På Galderma i Uppsala har vi verksamhet inom produktutveckling och tillverkning inom dermatologi och vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Vi är belägna längs med Fyrisån i Uppsala, 10 minuters cykelfärd från Uppsala Resecentrum.



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag, dock senast 16 februari 2025. Urval och intervjuer görs löpande under ansökningstiden, och tjänsten kan komma att tillsättas innan sista ansökningsdatum.

* Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren.
* Nästa steg är en intervju med anställande chef
* Andra steget är en panelintervju med teamet
* Sista steget är en facklig intervju



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Job Title: Business Process Improvement Specialist - Planning

Location: Uppsala, Sweden (on site)



Job description:

The mission of the Business Process Improvement Specialist - Planning is to drive transformation and change in supply planning operations. This role focuses on delivering process excellence by analyzing, developing, and optimizing business processes within the planning team. Key objectives include improving operational efficiency, quality, and customer satisfaction through data-driven decision-making and continuous improvement initiatives. The specialist will collaborate with cross-functional teams, provide training and support for new processes, and lead projects from inception to completion.



Key responsibilities:

*

Process Analysis: Evaluate existing business processes to identify inefficiencies or bottlenecks, requiring a strong analytical mindset, attention to detail, and excellent problem-solving skills.
*

Solution Development: Develop solutions to address identified process gaps, which may involve researching new technologies, tools, or methodologies to streamline processes and increase productivity. Work closely with cross-functional teams such as IT, operations, finance, and human resources to effectively implement these solutions.
*

Continuous Improvement: Drive continuous improvement initiatives within the organization, focusing on both short-term fixes and long-term sustainability. Establish performance metrics and track progress to ensure implemented changes yield positive results.
*

Team Collaboration: Collaborate with cross-functional teams, including supply chain, production, warehouse, customer service and quality assurance, to ensure alignment and effective implementation of process improvements.
*

Performance Monitoring: Establish key performance indicators (KPIs) and monitor progress against goals, providing regular updates to senior management.
*

Training and Support: Provide training and support to team members on new processes and tools to ensure successful adoption and execution. Maintain thorough documentation of processes, improvements, and outcomes to ensure transparency and knowledge sharing.
*

Project Management: Lead and manage process improvement projects from inception to completion, ensuring timely delivery and successful outcomes.



Skills & Qualifications

*

Master or Bachelor's degree in supply chain, or equivalent experience/qualification
*

Minimum of 8 years of experience in demand / supply planning within industrial environment, brings in industry best practices
*

Fluent in English and Swedish





What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.



We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10-minute bike ride from Uppsala Central Station.



Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as possible, as the selection process is ongoing continuously.

*

If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
*

The next step is an interview with the hiring manager
*

The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else.



At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.



Job Title: Plant Direct & Indirect Buyer
Location: Uppsala, Sweden (hybrid)



Job Description

Are you a strategic and proactive professional ready to lead sourcing initiatives that drive operational excellence and cost efficiencies? Join us as a Plant Direct & Indirect Buyer and play a key role in shaping our procurement strategies for direct materials and professional services. This is an exciting opportunity to contribute to a thriving organization in the life sciences industry, where your expertise will directly support our financial objectives and operational growth.



Key Responsibilities

* Develop and execute sourcing strategies for direct materials and professional services, ensuring alignment with Galderma's financial goals.
* Lead supplier negotiations to secure optimal pricing, terms, and quality.
* Analyze market trends, cost drivers, and feedstock dynamics to anticipate changes and drive value.
* Maintain spend tracking and propose budgets with clear savings targets, providing accurate forecasts and price variance analyses.
* Implement a multi-sourcing approach, conduct regular tenders, and perform cost breakdown analyses to enhance supplier competition and mitigate risks.
* Manage supplier performance through structured business reviews and maintain updated risk assessments with contingency plans.
* Support new product introductions and project launches, acting as project manager when
*



Skills & Qualifications

* Bachelor's degree in Business, Engineering, or a related field; a Master's in Purchasing is highly desirable.
* Experience from the Life Science industry is required.
* Some years of purchasing experience is beneficial.
* Strong negotiation and analytical skills, with a solid understanding of technical, financial, and market dynamics.
* Proficiency in ERP systems, with experience in M3 being an advantage.
* Demonstrated knowledge of risk management, legal compliance, and responsible sourcing practices.
* Experience in the life sciences sector is highly valued.



What we offer in return
You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.



We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.



Next steps
We welcome your application via our company website CAREERS | Galderma. If you are currently an employee of Galderma, we welcome your application via our internal career site via Workday. The selection process is ongoing and the role may be filled prior the last application date.

* If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
* The next step is a virtual conversation with the hiring manager
* The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else.



At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.



Job Title: Process Engineer (Aseptics)
Location: Uppsala, Sweden (onsite)



Job Description

Join Galderma as a Process Engineer, where you'll play a key role in enhancing our operations. With a focus on aseptic processes, you will apply your expertise to optimize production systems, uphold safety and compliance, and collaborate with cross-functional teams.



Key Responsibilities

*

Develop, implement, and optimize aseptic manufacturing processes to meet quality, safety, and compliance standards.
*

Collaborate with cross-functional teams to analyse and resolve technical challenges in production, leveraging prior experience and innovative thinking.
*

Support engineering activities to modify and improve existing aseptic processes, develop new test procedures and policies for aseptic environment, ensuring alignment with operational goals
*

Participate in risk analysis and troubleshooting, maintaining focus on aseptic standards to ensure contamination-free operations.
*

Monitor technology trends and support the deployment of engineering solutions that enhance reliability, cost-effectiveness, and efficiency.
*

Provide technical support during audits and inspections, ensuring adherence to regulatory and company standards.



Skills & Qualifications

*

Bachelor's Degree in Engineering with work experience within pharma, or Bachelor's Degree in Biology, Chemistry with experience from working with process engineering, or equivalent experience.
*

Some years of experience from industry, preferably within aseptic manufacturing.
*

Strong problem-solving skills and the ability to work independently with moderate supervision.
*

Familiarity with quality standards and risk management processes in regulated environments.
*

Fluent in Swedish and English.



What we offer in return
You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.



We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.



Next steps
We welcome your application via our company website CAREERS | Galderma. If you are currently an employee of Galderma, we welcome your application via our internal career site via Workday. The selection process is ongoing and the role may be filled prior the last application date.



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If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
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The next step is a virtual conversation with the hiring manager
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The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.