Uppsala: Manager MSAT Device Injectables

Hitta ansökningsinfo om jobbet Manager MSAT Device Injectables i Uppsala. Är det intressant kan du gå vidare och ansöka jobbet. Annars kan du klicka på arbetsgivaren eller yrkesbenämningen för att se alla jobb i Uppsala inom den kategorin.

Publicerad: 2025-10-01 // Varaktighet: Heltid

Job Title: Manager MSAT Device Injectables

Location: Uppsala, Sweden (Hybrid)

Job description:

In this exciting leadership role, you'll manage a skilled team of scientists working with Device Injectables - focused on both new product implementation (NPI) and commercial production support.

Together, you'll turn cutting-edge technologies into real-world manufacturing capabilities by applying science, solving problems, and driving continuous improvement.

You'll play a key part in bridging innovation and production - ensuring that what's developed in R&D can be scaled, validated, and successfully transferred to manufacturing.



Key responsibilities:

As Manager MSAT Device Injectables, you and your team will:

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Lead NPI activities - from early prototyping to full-scale manufacturing
*

Ensure smooth tech transfer from R&D into commercial production
*

Own and optimize end-to-end assembly and packaging processes
*

Ensure design solutions from engineering teams support manufacturing efficiency, reliability, and quality
*

Develop and validate processes for bulk and fill-finish manufacturing of injectable device products
*

Drive process validation (PV), trending, and continuous process verification (CPV)
*

Provide expert technical support for daily operations, audits, and regulatory submissions
*

Own change controls and ensure compliance with all relevant regulatory frameworks (LoRR, MDR, etc.)
*

Be responsible for process material specifications and post-validation documentation
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Own design control documentation after product transfer to production



In this role, you'll collaborate closely with QA, Engineering, R&D, Regulatory Affairs, and external partners - helping to solve complex challenges and enable seamless production.

You'll also serve as a trusted advisor to senior leaders, guiding them on best practices, systems, and process strategies to ensure high performance across functions.

Skills & Qualifications

We're looking for a pragmatic, hands-on leader with a deep understanding of injectable manufacturing - someone who thrives where science meets execution and isn't afraid to take technical ownership.

You bring experience from the shop floor to senior decision-making, and you know how to drive products from R&D into full-scale production - efficiently, compliantly, and collaboratively.



You're likely a great match if you have:

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8+ years in biopharma or medical device manufacturing, especially with injectables
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Solid knowledge of bulk formulation, sterile filtration, fill-finish (syringes, vials), visual inspection, and sterilization
*

Strong background in tech transfer, process validation (IQ, OQ, PQ, PPQ, FAT, SAT), and commercial manufacturing
*

Hands-on experience managing CAPA, deviations, audits, and documentation ownership
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Proven ability to lead process implementation, equipment qualification (including URS), and supplier collaboration - ideally with CAPEX exposure
*

Familiarity with GMP, ISO 13485, 21 CFR Part 11, and MDR
*

End-to-end process responsibility: from design input to commercial readiness
*

Leadership experience with at least 2 direct reports
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Excellent communicator, confident across functions like QA, R&D, Production, and Engineering
*

Fluent in English (Swedish is a plus)



Bonus points if you bring:

*

Skills in problem-solving frameworks (e.g. 5 Whys, FMEA, Ishikawa)
*

Experience in global or matrix-driven organizations
*

A project management certification (PMP, PRINCE2, or equivalent)

Why Join Galderma in Uppsala?

Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics - home to over 800 professionals working across R&D, manufacturing, clinical development, and marketing, all under one roof.

You'll be part of a multidisciplinary team where science meets application.



What we offer:

· Career development & learning opportunities

· Attractive benefits and bonus models

· Innovative projects

· Global & inclusive culture

· Strong team spirit & engagement

· Work-life balance & wellbeing



Are You the One We're Looking For?

We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

At Galderma, we actively give our teams reasons to believe in our bold 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.

Q-Med AB

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Andra jobb i Uppsala som Civilingenjör, forskning/utveckling, kemi

Nedan visas andra jobb i Uppsala som Civilingenjör, forskning/utveckling, kemi.

Technical Specialist – Material Development and Process Engineering

Besca AB
Civilingenjör, forskning/utveckling, kemi
Läs mer Jun 7
About the Company
Besca is a Swedish deeptech startup developing advanced carbon materials from renewable resources. Our solutions enable sustainable battery production and efficient water purification through breakthrough biomass refining using plasma technology. We are a research-driven team with strong international expertise, based in Uppsala and Stockholm.


Job Responsibilities
We are now looking for a Technical Specialist in material technology who will play a central role in our technology development. The role includes:
- Leading the development of carbon-based material through biomass carbonization
- Defining and specifying components in our process equipment, including plasma and microwave units
- Contributing to the development of testing protocols and material analysis
- Supporting work related to intellectual property and innovation


Required Qualifications
- Master’s degree (or equivalent) in Materials Science, Chemical Engineering, Physics, or a related field
- Documented experience in carbonization of biomass or other organic materials
- Practical experience with plasma technology and/or microwave-based thermal processes
- Ability to work in a laboratory and R&D environment
- Fluent in English (spoken and written)


Meriting Qualifications
- Experience from startup environments
- Knowledge of material characterization and analytical methods
- PhD’s degree (or equivalent) in Materials Science, Chemical Engineering, Physics, or a related field
- Familiarity with IP and patent work


Terms and Benefits
Location: Uppsala
Scope: Part-time, 75%
Duration: Permanent, with 6-month probation
Application: CV and cover letter to be sent to info@bescacarbon.com
Start: As soon as possible. Interviews are conducted on a rolling basis.
Benefits: Generous pension contributions and the opportunity to participate in the company’s stock option program
Besca is in an early commercialization phase, which is reflected in moderate salary level. However, employees are offered long-term incentives through employee stock options and the opportunity to build deep expertise in a future-oriented field.
We are looking forward to your application!

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Senior Scientist - Oligonucleotide Synthesis

Cytiva Sweden AB
Civilingenjör, forskning/utveckling, kemi
Läs mer Jun 4
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible.
We are looking for a Senior Scientist to join our team in Uppsala. As part of Nucleic Acids R&D, you will play a key role in developing innovative products that are used in the manufacturing of leading biological drugs. Your work will span the full development lifecycle—from idea generation and research to development and continuous improvement—while also contributing to troubleshooting and optimisation of existing Cytiva processes.
The Uppsala site is a key hub within Cytiva, with more than 1,500 employees across functions such as manufacturing, marketing, quality control, and quality assurance. Collaboration is therefore central to this role, and you will work closely with cross-functional partners to drive projects forward and deliver high-quality solutions.
You will join the Nucleic Acids section within the Genomic Medicine Operating Company, R&D Uppsala. Our team consists of 16 researchers working across production, purification, filtration, and analytical characterisation of nucleic acids, supporting product development to meet our customers’ needs. We are now looking to strengthen the team with an expert in oligonucleotide synthesis who can bring deep technical expertise and contribute to our continued innovation.
What you will do:
Act as a subject matter expert in oligonucleotide synthesis, including phosphoramidite chemistry, solid supports, and synthesis optimization.
Conduct analysis and method-related work in new product development, product care, and market support projects, with a strong customer focus.
Develop analytical methods to characterize oligonucleotides such as HPLC, LCMS or mass spectrometer.
Lead and own the automated oligonucleotide synthesis workflow, including instrument configuration, method setup, advanced troubleshooting, and performance optimization across different oligo sequences and applications.
Lead method development, optimization, verification, and validation activities, ensuring robustness, reproducibility, and alignment with design control and regulatory expectations.
Independently plan, execute, and document experimental work in a structured manner.
Present and communicate results at project meetings, in customer interactions, and occasionally through posters or oral presentations at conferences.
Act as a technical advisor to customer-facing and commercial teams, supporting complex customer queries related to oligonucleotide synthesis and nucleic acid workflows.

Who you are:
You hold a PhD (5+ years experience) or BSc/MSc (8+ years experience) in chemistry, biochemistry, biotechnology preferable from industry experience.
You have hands-on experience in oligonucleotide synthesis, including phosphoramidite chemistry and solid support synthesis.
You have solid experience working in design control.
You have experience with method development, verification, and validation, preferably in a regulated or industrial R&D environment.
You are comfortable configuring automated oligonucleotide synthesizer including synthesis protocols and instrument settings and troubleshooting both chemistry- and hardware-related issues.
Experience working with chromatography systems and UNICORN™ software is considered a strong advantage.
You are collaborative, structured, and self-driven, and enjoy working in a dynamic, cross-functional, and customer-focused environment.
You have strong presentation and communication skills, with advanced proficiency in English (written and spoken).
You hold a valid Swedish work permit.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.

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Forskare inom utveckling av PINN-modell för massatillverkning

Uppsala Universitet
Civilingenjör, forskning/utveckling, kemi
Läs mer Apr 17
Vid avdelningen för tillämpad mekanik, institutionen för materialvetenskap, Uppsala Universitet
Tidsbegränsad heltidsanställning om 9 månader, med start enligt överenskommelse.
Bli en av oss! 
Institutionen för materialvetenskap har som mål att vara en miljö för framgångsrik och värdefull forskning och utbildning med inriktning mot materialvetenskapliga lösningar för viktiga samhällsutmaningar. Vår institution är en spännande arbetsplats med forskning i ett brett teknikrelaterat område, från grundforskning till storskalig tillämpad forskning, och har täta kontakter med studenter genom institutionens engagemang i civilingenjörs- kandidat- och masterutbildningar. Institutionen har sju avdelningar med olika forskningsfokus, samt en administrativ avdelning för stöd och service. Institutionen är en internationell arbetsplats med ca 230 verksamma medarbetare. 
Läs mer om oss här 
Om avdelningen
Avdelningen för tillämpad mekanik är en del av Institutionen för materialvetenskap och teknik vid Ångströmlaboratoriet. Vi bedriver forskning inom experimentell och beräkningsinriktad mekanik med tillämpningsområden främst inom livsvetenskaper, material- och strukturutveckling samt energirelaterade områden. Den forskning som bedrivs är ofta tvärvetenskaplig och sträcker sig från tillämpade projekt i nära samarbete med industri till akademisk grundforskning.
Projektbeskrivning
I detta pilotprojekt utvecklas ett digitalt modelleringsverktyg som kopplar samman molekylära simuleringar av lignin med processmodeller för massakok. Med hjälp av molekyldynamiska simuleringar (MD) analyseras hur ligninets kemiska struktur påverkar tillgänglighet, packning och transportegenskaper på mikroskopisk nivå. MD-resultaten integreras i en Physics-Informed Neural Network (PINN), där etablerade fysikaliska samband för diffusion, reaktion och massbalans byggs in i modellen. PINN-modellen fungerar därmed som ett uppskalningsverktyg som översätter molekylära skillnader i råvaran till processrelevanta parametrar på kokerinivå.
Projektet utförs i dialog med företag inom skogsindustrin.
Arbetsuppgifter
Du ansvarar för att utveckla en PINN-modell baserad på resultat från MD-simuleringar. Du utgår ifrån mätbara industriellt relevanta processparametrar och optimerar dessa genom att integrera resultat från atomistisk modellering i ett Physics Informed Neural Network (PINN). Exempel på industriella processparametrar som skulle kunna vara relevanta är kappatal, massautbyte eller kemikalieanvändning.
I arbetsuppgifterna ingår även skriftlig dokumentation och kommunikation av forskningsresultat och presentationer vid informella seminarier samt samverkan med skogsindustrin.

Kvalifikationskrav
För anställning som forskare ska du ha doktorsexamen, eller en utländsk examen som bedöms motsvara doktorsexamen.
För denna anställning krävs:
En doktorsexamen inom beräkningskemi, materialvetenskap, teknisk/teoretisk fysik eller motsvarande examen inom angränsande område.
Dokumenterad kunskap och erfarenhet av molekyldynamiska simuleringar.
Mycket goda skriftliga och muntliga färdigheter i engelska,
Mycket goda färdigheter att skriva vetenskapliga publikationer.

Meriterande/önskvärt i övrigt
Erfarenhet av MD-simuleringar av vedpolymerer
Dokumenterade kunskaper om processerna i ett massabruk
Programmeringsvana
Erfarenhet av samverkan mellan industri och akademi
Erfarenhet av PINN-modellering eller andra maskininlärningsmetoder

Vi lägger stor vikt vid dina personliga egenskaper och du måste vara självgående och initiativrik och ha förmåga att självständigt planera och driva projekt. Du skall vidare vara strukturerad och kunna arbeta effektivt både enskilt och i grupp, samt ha lätt för att samarbeta och kommunicera i tvärvetenskapliga sammanhang.
Instruktioner för ansökan
Din ansökan ska innehålla:
Ett kort brev där du beskriver dig själv, varför du är intresserad av detta projekt och varför du är lämplig för denna tjänst
CV (max 2 sidor)
Kopia på doktorsexamen, masterexamen (eller motsvarande) och kursbetyg
Publikationslista. Markera de mest relevanta publikationerna för tjänsten samt kommentera vad du bidragit med i just dessa publikationer.
Namn och kontaktuppgifter på minst två personer som har accepterad att vara referenser för dig. Det ska även framgå vilken relation du har haft till respektive referent.

Ansökan kan med fördel skrivas på engelska. Vi kommer löpande under ansökningstiden att läsa ansökningshandlingar och kalla till intervju.
Om anställningen: Anställningen är tidsbegränsad, 9 månader. Omfattningen är 100%. Tillträde enl överenskommelse. Placeringsort: Uppsala
Upplysningar om anställningen lämnas av:
Universitetslektor Malin Wohlert, malin.wohlert@angstrom.uu.se
Välkommen med din ansökan senast den 10 Maj 2026, UFV-PA 2026/1156
Uppsala universitet är ett brett forskningsuniversitet med stark internationell ställning. Det yttersta målet är att bedriva utbildning och forskning av högsta kvalitet och relevans för att göra skillnad i samhället. Vår viktigaste tillgång är alla 7 500 anställda och 53 000 studenter som med nyfikenhet och engagemang gör Uppsala universitet till en av landets mest spännande arbetsplatser.
Läs mer om våra förmåner och hur det är att jobba inom Uppsala universitet
https://uu.se/om-uu/jobba-hos-oss/
Anställningen kan komma att säkerhetsprövas. Vid säkerhetsprövning är en förutsättning för anställning att sökande blir godkänd.
Vi undanber oss erbjudanden om rekryterings- och annonseringshjälp.
Ansökan tas emot i Uppsala universitets rekryteringssystem.
Fackliga företrädare: Saco-S - saco-s@uu.se, Seko - seko@uadm.uu.se, ST (OFR/S) - ofr@uu.se

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Senior Research Engineer, Sunresin

SallyQ AB
Civilingenjör, forskning/utveckling, kemi
Läs mer Mar 2
Sunresin is a newly established subsidiary of a leading global manufacturer of chromatography resins, now building its European hub in Uppsala, Sweden. The site brings together research, development, and production of agarose-based chromatography resins and affinity ligands, supported by a strong multinational group. 
The lab at the Sunresin Uppsala site is starting to take form and most things are coming into place. Therefore, they are looking for a Research engineer to join the team. 
The Role 
As a Research Engineer, you will strengthen the analytical team at the new Uppsala site. In this role, you will contribute hands-on in the laboratory in close collaboration with research and development, with a primary focus on supporting the development of protein purification processes and chromatography media. As Sunresin at Uppsala is in a start-up phase the role will evolve as Sunresin grows and it is a good fit for someone who likes taking on new responsibilities without losing structure or direction.  
Your responsibilities will include implementing and validating immunoassays, as well as establishing and performing other analytical methods.
Duties & Responsibilities 
Implement and validate immunoassays, primarily ELISA. 


Perform and optimize electrophoresis-based methods. 


Support protein purification process development through analytical characterization. 


Conduct protein identification, quantification, and activity assays. 


Perform HPLC and other relevant analytical techniques. 


Document and ensure quality compliance according to applicable standards. 


Collaborate cross-functionally with resin chemistry, ligand development, and production teams. 


The company is located in Uppsala Business Park, and you will be part of a growing team.? 
Your Profile 
You hold a degree in Biotechnology, Chemistry, Biochemistry, or a related field, and have hands-on laboratory experience in protein analytics.  
You have demonstrated experience in: 

Independently implementing and validating ELISA methods.


Working with electrophoresis techniques.


Applying protein analytical methods such as HPLC, activity assays, and quantification methods.


As a person, you are structured, analytical, and curious. You thrive in a hands-on role that combines laboratory work with problem-solving and cross-functional collaboration. You are comfortable in a growing organization where processes and structures are still evolving. This role suits someone who remains confident even when not all the answers are in place, you take ownership of your work and collaborate closely with colleagues to find the right way forward. 
You are fluent in English; Swedish is considered an advantage.
Application? 
Please send in your application no later than the 13 March. If you have any questions, please do not hesitate to reach out to recruiter Hanna Peterson at SallyQ - phone: +46 (0)73-940 57 98 or email: hanna.peterson@sallyq.se
About Sunresin 
Sunresin is a newly established Swedish subsidiary of a leading global manufacturer of chromatography resins, with annual revenues exceeding $360M. The company has a long-standing reputation for delivering high-quality solutions that enable the purification of biopharmaceuticals worldwide. The Uppsala site marks a strategic expansion, serving as the European hub for the development and production of agarose-based chromatography resins and affinity ligands. They are now building a high-performing team that combines research, development, and manufacturing capabilities under one roof. The site will play a central role in advancing resin chemistry, ligand development, and operational excellence, contributing to the global supply of critical materials for biopharmaceutical purification. Backed by the strength of a multinational group and driven by innovation at the local level, we are creating an environment where expertise, collaboration, and growth go hand in hand. Our mission is to provide cutting-edge purification technologies that support the development of life-saving therapies worldwide.

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Process Development Engineer, Biologics

Q-Med AB
Civilingenjör, forskning/utveckling, kemi
Läs mer Feb 25
Job Title: Process Development Engineer, Biologics (Drug Substance or 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 Process Development Engineer is a subject matter expert (SME) responsible for new product implementation (NPI) into a manufacturing facility.



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)
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Write and review technical documentation ensuring compliance with regulatory and quality standards.
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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.
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Prepare detailed investigation reports, conveying findings and recommendations to management and relevant stakeholders



Skills & Qualifications

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BSc or MSc in a relevant scientific or engineering field, such as Chemistry, Biochemistry, Chemical Engineering, or related discipline
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Minimum of 2 years of experience in a biopharmaceutical environment
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Familiarity with manufacturing processes in the biopharmaceutical industry
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Experience in investigative methodologies and root cause analysis techniques





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.

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Andra jobb i Uppsala från Q-Med AB

Nedan visas andra jobb i Uppsala från Q-Med AB .

Senior Automation Engineer

Q-Med AB
Automationsingenjör, maskin
Läs mer Mar 31
We're now looking for a passionate and driven Automation Engineer to join our Operations Engineering team in Uppsala and play a key role in shaping the future of manufacturing automation at Galderma. If you thrive in a GMP-regulated environment, enjoy solving complex technical challenges, and want to make a real impact on production performance and reliability - this is your opportunity.

At Galderma, we're not just offering a job - we're inviting you to be part of something bigger. As a global leader in dermatology, we combine purpose with innovation to improve the lives of millions.



About Galderma:

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.



Job Description

As an Automation Engineer based in Uppsala, you will manage, plan, and oversee the implementation of engineering plans and programs related to operational automation systems and manufacturing lines. You will ensure that systems meet required safety, quality, compliance, and performance standards within a GMP-regulated environment.

In this role, you will develop and execute engineering plans, analyze trends and recurring issues in manufacturing automation systems, and provide robust, sustainable solutions that secure high system availability and optimized Overall Equipment Effectiveness (OEE). You will collaborate closely with cross-functional teams, represent Engineering in projects, and maintain strong relationships with internal stakeholders and external suppliers.

You will act as an individual contributor with recognized intermediate expertise in automation, working independently with moderate supervision while contributing to coordination across engineering and operational areas.

Key Responsibilities

In this position, you will play a central role in ensuring reliable and compliant automation systems that support our manufacturing operations. Your responsibilities include:

* Providing expert troubleshooting and maintenance support for existing automation systems, ensuring maximum uptime and system performance.
* Programming and configuring automation systems including PLCs, HMIs, SCADA platforms, and related control systems.
* Supporting the design and development of automation solutions for biopharmaceutical manufacturing processes.
* Collaborating with cross-functional teams to ensure alignment with site standards, project requirements, and engineering strategies.
* Implementing best practices to enhance system reliability, scalability, and Overall Equipment Efficiency (OEE).
* Creating automation-related change controls and executing Computer System Validation (CSV) activities in accordance with GMP and Part 11 requirements.
* Investigating automation-related deviations, supporting root cause analysis (RCA/RCCA), and implementing corrective and preventive actions.
* Performing automation computer system support activities such as system backups, performance monitoring, and user/password administration.
* Providing technical support for automation control platforms and process information systems (e.g., data historians).
* Contributing to capital project execution and supporting machinery/system design activities.
* Ensuring all work is executed in compliance with GMP, internal policies, procedures, safety rules, and regulatory standards, including participation in internal and regulatory audits.



Key Requirements & Qualifications

We are looking for a technically skilled and solution-oriented professional who combines analytical thinking with hands-on capability in automated production environments.

* Bachelor's degree in Electrical Engineering, Control Engineering, Electronic Engineering, or equivalent experience.
* Minimum of 3 years' experience configuring and supporting automation systems, including PLCs, HMIs, and SCADA solutions.
* Experience working in a GMP-regulated environment and familiarity with Part 11 requirements, or experience from a similarly regulated industry.
* Experience with SCADA systems and related platforms such as Siemens, WinCC, iFix, Wonderware, and data historians.
* Experience in capital project execution and/or machinery or system design is considered an advantage.
* Professional level of English; Swedish is desirable.
* Solid understanding of project management processes and structured problem-solving methodologies.



Why Join Galderma in Uppsala?

Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics - home to over 800 professionals working across R&D, manufacturing, clinical development, and marketing, all under one roof. You'll be part of a multidisciplinary team where science meets application.



About Galderma:
Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

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Sr Project Manager

Q-Med AB
Civilingenjör, process, kemiteknik
Läs mer Mar 31
Job Title: Senior Project Manager Life Sciences (R&D)

Location: Location: Uppsala, Sweden - Hybrid



We're now looking for an experienced and business-driven Senior Project Manager within Therapeutic Injectables (R&D) to join our team in Uppsala. In this pivotal role, you will lead complex drug development projects, working at the heart of innovation where science, strategy, and execution meet. If you thrive in a cross-functional global environment and are motivated by turning ambitious R&D plans into reality - this is your opportunity to make a real impact.

If you're ready to bring science to life and make an impact beyond the lab - this is your chance.

At Galderma, we're not just offering a job - we're inviting you to be part of something bigger. As a global leader in dermatology, we combine purpose with innovation to improve the lives of millions.



About Galderma:
Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.



Job Description

As Senior Project Manager Life Sciences (R&D), you will work in close partnership with Program Franchise Head(s) and cross-functional project team members to establish and maintain integrated project plans and budgets. You will organize and lead structured project team meetings, foster transparent communication, and coordinate activities across multiple functional areas. You are accountable for driving the operational execution of project plans - both internally and in collaboration with external partners - ensuring that strategic objectives are translated into timely, high-quality deliverables.



Key Responsibilities

* Oversee and manage the effective coordination and facilitation of cross-functional R&D project team meetings, ensuring clear agendas, structured preparation, and timely documentation of decisions and actions to maintain momentum and alignment.
* Develop and manage global, integrated cross-functional project plans by identifying key deliverables, mapping interdependencies, driving alignment and accountability, coordinating project-level budget and resource forecasting, managing procurement activities, monitoring timelines, identifying risks and issues, and ensuring proactive follow-up on actions.
* Collaborate with stakeholders to create, organize, and continuously optimize project plans and timelines, while executing R&D project and portfolio management processes related to prioritization, resource allocation, and risk management.
* Proactively identify constraints, risks, and conflicts that may impact scope, budget, or timelines, and work closely with internal teams, senior management, and external business partners to develop sustainable solutions and ensure contractual deliverables are met.



Key Requirements & Qualifications



* A minimum of 5 years of relevant experience within pharmaceutical, life sciences, or a related regulated industry, combined with at least 5 years of leadership or management experience in complex environments.
* 3-5 years of hands-on experience in drug development project management, supporting functions such as Research, Clinical Operations, Regulatory Affairs, Medical Affairs, or Clinical Development sub-teams, with strong knowledge of the drug development lifecycle.
* Demonstrated ability to balance strategic thinking with operational execution, supported by strong interpersonal, negotiation, and stakeholder management skills, and the confidence to interface effectively with all organizational levels.
* Strong communication skills in English (verbal and written), financial and resource planning expertise, and hands-on experience with project management tools such as Planisware, MS Project, MS Teams, Smartsheet, or PowerBI. You are self-directed, process-oriented, and recognized for your creativity and foresight in solving complex project challenges.



Why Join Galderma in Uppsala?

Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics - home to over 800 professionals working across R&D, manufacturing, clinical development, and marketing, all under one roof.
You'll be part of a multidisciplinary team where science meets application.



What we offer:

* Career development & learning opportunities
* Attractive benefits and bonus models
* Innovative projects
* Global & inclusive culture
* Strong team spirit & engagement
* Work-life balance & wellbeing



Are You the One We're Looking For?
We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.
At Galderma, we actively give our teams reasons to believe in our bold 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.

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Classified Areas Engineer

Q-Med AB
Pressare, kläder
Läs mer Mar 25
Vill du arbeta i en högteknologisk och regulatoriskt styrd miljö där kvalitet, säkerhet och innovation står i fokus? Vi söker nu en Classified Areas Engineer som vill bidra till utveckling och drift av våra renhetsklassificerade tillverkningslokaler.



Om rollen

Som Classified Areas Engineer hos Galderma arbetar du i huvudsak med att ansvara för drift och underhåll av tillverkningslokaler där produktion sker. Dessa tillverkningslokaler har olika nivåer av renhetskrav, t.ex. renrum EU GMP Grade C och D samt ISO Klass 7 och 8. Under ansvaret finns även tillverkningslokaler som inte är klassificerade enligt externa regelverk, som monitoreras med avseende på temperatur och luftfuktighet.

Som Classified Areas Engineer ansvarar du för att tillverkningslokalerna är i gott skick och uppfyller de krav som ställs gällande hygienisk design. Samordna underhållsaktiviteter inom ansvarsområdet som t.ex. kontroller av HEPA filter, dörrar, slussar samt städning som utförs till större del av externa parter. Skapa och underhålla instruktioner, utreda avvikelser och utföra korrigerande och förebyggande åtgärder.

För den här rollen så är fokus på den nya fabrik som byggts på siten där vissa delar redan är i drift medan andra delar fortfarande är i projektfas (bland annat renrum EU GMP Grade C och D). Classified Areas Engineer rollen är en viktig spelare i övergången från projektfas till drift och produktion.

Du får en viktig roll i att säkerställa att våra processer, system och miljöer uppfyller högt ställda krav inom kvalitet, säkerhet och regelefterlevnad.

Du kommer att arbeta självständigt med stöd från erfarna kollegor och samarbeta brett inom organisationen.



Huvudsakliga ansvarsområden

* Implementera och följa upp ingenjörsplaner och processer
* Övervaka och hantera driften av klassade områden och säkerställa efterlevnad av säkerhetsstandarder och myndighetskrav.
* Utföra arbete i enlighet med ISO?standarder, CFR, cGMP samt Galdermas SOP:er och policys.
* Ansvara för underhållsprogram för klassade områden såsom (men inte begränsat till) EU GMP Grade C och D samt ISO 7 och 8, inklusive sitens CNC?områden (Controlled Not Classified).
* Utföra och leda tekniker i felsökning inom avdelningens definierade ansvarsområden.
* Ansvara för planering av fältmätningar, provanalyser och rutinmässiga driftaktiviteter som faller under avdelningens ansvar.
* Rapportera, utreda och stänga avvikelser samt genomföra CAPA och effektivitetskontroll i enlighet med Galdermas kvalitetsledningssystem.

Övervaka systemprestanda via automatiserade system såsom BMS (Building Management System), UMS (Utility Management System) och EMS (Environmental Management System)

Din profil

Du är en analytisk och lösningsorienterad ingenjör som trivs i en komplex miljö och har ett starkt kvalitetstänk. Du arbetar strukturerat, tar ansvar och har god samarbetsförmåga.

Kvalifikationer

* Kandidatexamen inom relevant tekniskt område (eller motsvarande)
* 2-5 års erfarenhet inom teknik/ingenjörsarbete
* Erfarenhet från läkemedel, tillverkning eller reglerad verksamhet är meriterande
* God kunskap om cGMP, ISO-standarder eller liknande
* Flytande svenska och engelska

Varför Galderma?

Hos oss får du arbeta i en global organisation där innovation möter verklighet. Du blir en del av ett engagerat team och bidrar till produkter som gör verklig skillnad för patienter världen över.

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HRBP

Q-Med AB
HR-specialist/HR-adviser
Läs mer Mar 23
Vi söker nu en erfaren och affärsdriven HR Business Partner som vill spela en nyckelroll i att utveckla både verksamhet och människor i vår organisation i Uppsala.
Om du drivs av att arbeta nära verksamheten, påverka strategiska beslut och skapa verklig förändring - då är detta din chans.

På Galderma erbjuder vi inte bara ett jobb - vi bjuder in dig att bli en del av något större. Som en global ledare inom dermatologi kombinerar vi syfte med innovation för att förbättra livet för miljontals människor.

I denna roll får du möjlighet att arbeta nära ledare och verksamhet för att driva HR-agendan framåt. Du kommer att vara en strategisk partner i förändringsresor, samtidigt som du säkerställer att våra HR-processer skapar värde för både organisationen och våra medarbetare. Här får du en unik möjlighet att kombinera operativt arbete med strategiskt inflytande i en global och dynamisk miljö.

Om Galderma:

Galderma är en framväxande, renodlad global ledare inom dermatologi och finns representerade i cirka 90 länder. Vi erbjuder en innovativ och vetenskapsbaserad portfölj av premiumprodukter och tjänster som täcker hela det snabbt växande dermatologiområdet - från injicerbara estetiska behandlingar och dermatologisk hudvård till terapeutisk dermatologi.

Sedan starten 1981 har vi haft ett tydligt fokus på människokroppens största organ - huden. Genom nära samarbete med vårdpersonal möter vi individuella behov hos både konsumenter och patienter med lösningar som ger överlägsna resultat. Vi vet att huden vi är i formar våra liv - och därför driver vi dermatologin framåt för varje unik hudhistoria.

Arbetsbeskrivning

Som HR Business Partner kommer du att arbeta nära verksamheten och ansvara för att implementera och driva HR-strategier, processer och initiativ som stödjer affärens mål. Du fungerar som ett strategiskt och operativt stöd till chefer och säkerställer att HR-arbetet är i linje med verksamhetens behov och prioriteringar.

Rollen innebär att du aktivt bidrar till att utveckla och förbättra HR-processer, samtidigt som du driver förändringsinitiativ och stärker organisationens förmåga att nå sina mål. Du kommer att arbeta brett inom HR-området och ha en central roll i att skapa en engagerande och högpresterande organisation.

Ansvarsområden

* Du implementerar HR-strategier och HR Business Partner-planer för att säkerställa ett proaktivt och affärsnära HR-stöd till verksamheten, samt driver implementering av policys, processer och program.
* Du bidrar till att utveckla, förbättra och administrera HR-processer för att säkerställa kvalitet, effektivitet och relevans i hela organisationen.
* Du säkerställer att HR-aktiviteter är i linje med affärsstrategin och bidrar till att uppnå verksamhetens mål, samtidigt som du balanserar organisationens och medarbetarnas behov.
* Du driver förändrings- och transformationsinitiativ inom HR för att stärka organisationens kapacitet och utveckla ledarskap och medarbetarskap på alla nivåer.

Kvalifikationer och krav

* Du har en akademisk examen inom HR, beteendevetenskap, ekonomi eller motsvarande, samt gedigen erfarenhet av kvalificerat HR-arbete.
* Du har cirka 8-12 års erfarenhet inom HR, gärna i en roll som HR Business Partner eller motsvarande i en komplex organisation.
* Du är en etablerad expert inom ditt område och har erfarenhet av att driva större projekt, förändringsinitiativ och processförbättringar självständigt.
* Du har god förmåga att analysera affärsbehov, tolka organisatoriska utmaningar och omsätta dessa i konkreta HR-lösningar och rekommendationer.
* Du är trygg i att arbeta självständigt med stort ansvar och har förmåga att hantera komplexa frågor ur ett helhetsperspektiv.

Varför arbeta på Galderma i Uppsala?

Vår site i Uppsala är Galdermas globala center of excellence för estetik - med över 800 medarbetare inom R&D, produktion, klinisk utveckling och marknad, samlade under ett och samma tak.
Här blir du en del av ett tvärfunktionellt team där vetenskap möter praktisk tillämpning och där idéer snabbt kan omsättas till verklighet.

Vad vi erbjuder:

* Möjligheter till karriärutveckling och kontinuerligt lärande
* Konkurrenskraftiga förmåner och bonusmodeller
* Innovativa och meningsfulla projekt
* En global och inkluderande arbetskultur
* Stark teamkänsla och högt engagemang
* Balans mellan arbete och privatliv med fokus på välmående

Är du den vi söker?

Vi söker personer som fokuserar på resultat, har en stark vilja att lära och bidrar med positiv energi. Du kombinerar eget driv med god samarbetsförmåga och trivs i en miljö där man arbetar tillsammans för att nå gemensamma mål.

Framför allt drivs du av att göra något meningsfullt för konsumenter, patienter och de vårdprofessioner vi arbetar med varje dag. Vi strävar efter att stärka varje medarbetares utveckling samtidigt som vi möter verksamhetens behov - både nu och i framtiden.

På Galderma värnar vi om mångfald och respekterar varje individs värdighet, integritet och rättigheter. Vi skapar förutsättningar för våra team att tro på vår ambition att bli världsledande inom dermatologi. Hos oss får du möjligheten att utvecklas, utmanas och göra verklig skillnad.

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Project Controller

Q-Med AB
Finansekonom
Läs mer Mar 19
Project Controller

???? Uppsala, Sweden

We are looking for a Project Controller to join our Capital Portfolio Team. In this role you will support capital investment projects as well as non-investment projects within our Operations organization. In this role, you will provide financial oversight, analysis and reporting to ensure projects are delivered in line with budgets, forecasts, and financial governance.

Working in a highly regulated life sciences environment, you will collaborate closely with Project Managers, Engineering, Operations, and Finance to support effective financial planning, monitoring, and reporting of CAPEX and OPEX activities.

This role offers the opportunity to contribute to projects that support the development and manufacturing of innovative pharmaceutical and life science products that improve patients' lives.

About the Role

As a Project Controller, you will ensure strong financial governance and transparency across our projects portfolios. You will manage financial data, provide insights for decision-making, and act as the Finance partner to Project Managers and cost center owners supporting cost tracking, forecasting, and financial performance.

Key Responsibilities

* Provide financial reporting, analysis, and forecasting for capital projects within Operations.
* Support budget preparation, monitoring, and financial follow-up for project portfolios.
* Track, analyze, and report project financial data in line with company policies and financial systems.
* Act as the primary finance partner to Project Managers, supporting project cost control and forecasting.
* Support Line Managers with OPEX budgeting and financial follow-up.
* Review and approve purchase requests related to project and operational costs.
* Serve as system administrator for the financial project tracking tool and ensure compliance with financial governance.
* Represent Finance in cross-functional project meetings and present financial insights to stakeholders and leadership.
* Contribute to the continuous improvement of financial controlling processes.


Your Profile

You are an analytical and structured finance professional who can translate complex financial data into clear insights that support project decisions. You enjoy working cross-functionally and building strong relationships with stakeholders.

Qualifications

* Bachelor's or Master's degree in Finance, Accounting, Business Administration, or related field
* Approximately 5 years of experience in financial controlling, project controlling, or similar roles
* Experience from manufacturing, pharmaceutical, biotech, or life sciences environments is a strong advantage
* Fluent in Swedish and English

Skills

* Strong analytical and financial modeling skills
* Experience working with ERP systems and financial/project tracking tools
* Ability to manage complex financial data and end-to-end processes
* Strong communication and stakeholder management skills
* Proactive mindset with a focus on process improvement

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Senior Process Engineer -Aseptic Filling & Visual Inspection

Q-Med AB
Processutvecklare, kemi
Läs mer Mar 12
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.

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