Uppsala: Automation engineer

Job Title: Senior Automation Engineer

Location: Uppsala, Sweden (on site)



Job description:

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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.
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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.
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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:

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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.
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SCADA/PLC Programming: Develop, configure, and optimize SCADA systems and PLC programs for new projects, system upgrades, and continuous improvement initiatives.
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Automation System Design & Implementation: Lead the design, development, and commissioning of SCADA and PLC-based automation systems for pharmaceutical manufacturing operations.
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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.
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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.
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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.
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Documentation & Reporting: Create and maintain detailed technical documentation, including system designs, process flows, functional specifications, and user manuals.
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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.
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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

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Master's / bachelor's degree in electrical, control or electronic engineering
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Minimum of 8 years' experience in automation
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Previous experience within GMP and Part 11 or alternatively from a related regulatory industry.
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Experience with SCADA systems, historian, Siemens, WinCC, iFix, Wonderware, etc.
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Familiarity with robotics, motion control MES system
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Experience with configuring and programing vision system and machine learning software.
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Experience in capital project execution and machinery/system design.
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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.

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If your profile is a match, we will invite you for a first conversation with the recruiter.
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The next step is an interview 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.

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

Location: Uppsala, Sweden (on site)



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:

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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.
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Serve as a technical subject matter expert (SME) representing MS&T in Technology Transfer projects.
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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.
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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.
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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).
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Develop and lead execution of technical runs/design of experiments (DoE) with data analysis and recommendations.
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Maintain comprehensive records of investigations, findings, actions taken, and recommendations, ensuring compliance with regulatory and quality standards
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Write technical manufacturing documentation and dossier sections and provide responses to regulatory authorities as needed.
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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

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BSc, MSc, or PhD in a relevant scientific or engineering field, such as Chemistry, Biochemistry, Chemical Engineering, or a related discipline
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Prior manufacturing process experience within the biopharmaceutical industry with a minimum of 6 years of experience in a biopharmaceutical or manufacturing environment
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Experience in drug substance and/or drug product manufacturing within a GMP environment
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Previous experience of drug product manufacturing processes including compounding, filtration, aseptic filling (including setting up aseptic process simulation, APS) and visual inspection
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Experience with regulatory audits and regulatory requirements, risk management (FMEA), investigative methodologies and root cause analysis techniques is highly meriting
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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.

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.

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

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Develop, implement, and optimize aseptic manufacturing processes to meet quality, safety, and compliance standards.
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Collaborate with cross-functional teams to analyse and resolve technical challenges in production, leveraging prior experience and innovative thinking.
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Support engineering activities to modify and improve existing aseptic processes, develop new test procedures and policies for aseptic environment, ensuring alignment with operational goals
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Participate in risk analysis and troubleshooting, maintaining focus on aseptic standards to ensure contamination-free operations.
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Monitor technology trends and support the deployment of engineering solutions that enhance reliability, cost-effectiveness, and efficiency.
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Provide technical support during audits and inspections, ensuring adherence to regulatory and company standards.



Skills & Qualifications

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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.
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Some years of experience from industry, preferably within aseptic manufacturing.
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Strong problem-solving skills and the ability to work independently with moderate supervision.
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Familiarity with quality standards and risk management processes in regulated environments.
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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.



*

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.