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About this Manufacturing Scientist, Assembly & Packaging role at Galderma

Galderma · Onsite · Uppsala

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.

At Galderma, we advance dermatology for every skin story. As the pure-play dermatology category leader, we combine innovation, science, and manufacturing excellence to deliver solutions that improve the lives of patients worldwide.


We are now looking for a Senior Manufacturing Scientist to join our Manufacturing Science & Technology (MS&T) team in Uppsala. In this role, you will serve as a key technical expert supporting assembly and packaging operations, driving process performance, product quality, and continuous improvement through scientific expertise and data-driven decision-making.


The Role

As a Senior Manufacturing Scientist, you will provide technical oversight and process support for commercial manufacturing activities while partnering closely with production, quality, engineering, validation, and supply chain teams. You will play a central role in investigations, process optimization initiatives, and the application of analytical tools to improve operational excellence.


Key Responsibilities

  • Provide scientific and technical support for assembly and packaging processes.
  • Drive continuous improvement initiatives to enhance process robustness, efficiency, and product quality.
  • Lead and support complex investigations, root cause analyses, and implementation of effective corrective and preventive actions.
  • Analyze manufacturing and quality data to identify trends, risks, and opportunities for improvement.
  • Apply statistical and analytical methodologies to support process understanding and optimization.
  • Collaborate cross-functionally to resolve technical challenges and ensure reliable manufacturing operations.
  • Support regulatory inspections, audits, and compliance activities.
  • Ensure manufacturing processes operate in accordance with GMP requirements and applicable regulatory expectations.
  • Contribute technical expertise to validation, risk assessments, and change management activities.

Who You Are


You combine strong scientific knowledge with a practical manufacturing mindset. You enjoy solving complex technical problems, working with data, and influencing stakeholders across functions to deliver sustainable improvements.


Qualifications


  • Bachelor's, Master's, or PhD degree in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or another relevant scientific or engineering discipline.
  • Approximately 6-10 years of experience within biopharmaceutical, medical device, or manufacturing environments.
  • Strong experience in investigations, root cause analysis, and structured problem-solving methodologies.
  • Excellent analytical skills, including data collection, interpretation, and reporting.
  • Knowledge of cGMP requirements and regulatory frameworks.
  • Experience supporting inspections and regulatory audits.
  • Strong communication, documentation, and stakeholder management skills.

Technical Expertise


  • Assembly and packaging processes and manufacturing equipment.
  • Data analysis tools such as JMP, Minitab, Python, R, Power BI, or Spotfire.
  • Manufacturing systems including MES, LIMS, ERP, and SCADA.
  • Statistical and quality methodologies such as SPC, DOE, and Six Sigma.
  • GMP regulations and guidelines, including FDA, EMA, ICH, and Annex 1 requirements.
  • Validation principles, risk assessment, and quality-by-design approaches.

Preferred Qualifications


  • Six Sigma Green Belt or Black Belt certification.
  • Experience with digital validation systems and advanced analytics platforms.
  • Experience working in multi-site manufacturing organizations or CMO environments.

Why Join Galderma?


This is an opportunity to take on a highly visible role where science, manufacturing, and innovation come together. You will work in a collaborative environment alongside experienced colleagues while helping shape the future of manufacturing excellence at Galderma's Uppsala site. 


Join us and contribute to delivering high-quality products that make a meaningful difference for patients around the world.

Ready to apply to Galderma?
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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. For more

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