Sr Manufacturing Scientist -Cleaning Validation Expert

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.

We’re now looking for a passionate and driven MS&T Scientist – Cleaning Validation to join our team and ensure world-class contamination control and compliance in pharmaceutical manufacturing.
If you’re ready to bring science to life and make an impact beyond the lab — this is your chance.

At [Company Name], we’re not just offering a job — we’re inviting you to be part of something bigger. As a global leader in healthcare innovation, we combine purpose with technology to improve the lives of millions.

About Galderma:

Galderma is a global leader in pharmaceutical and biopharmaceutical solutions, present in over 90 countries. We deliver innovative, science-based products and services that meet the highest standards of quality and safety. Since our foundation, we have dedicated our focus and passion to advancing healthcare and improving patient outcomes worldwide.

Job Description

As an MS&T Scientist – Cleaning Validation, you will provide technical expertise and operational support for cleaning validation activities across pharmaceutical manufacturing processes. Your role ensures that equipment cleaning procedures are scientifically justified, compliant with global regulatory standards, and effective in preventing cross-contamination. You will collaborate with MS&T process owners, QA, and Production to deliver robust validation strategies and maintain inspection readiness.

Key Responsibilities

• Develop and validate cleaning processes (manual, CIP/SIP) and analytical methods (TOC, HPLC, LC-MS).
• Author and execute cleaning validation protocols and reports.
• Perform risk assessments and establish acceptance criteria based on regulatory guidance.
• Ensure compliance with GMP, FDA, EMA, ICH, and PIC/S guidelines.
• Support regulatory submissions and health authority inspections.
• Collaborate cross-functionally with Development, Production, QA, QC, and Engineering.
• Drive continuous improvement initiatives to optimize cleaning procedures and reduce downtime.

Key Requirements & Qualifications

• MSc/PhD in Pharmaceutical Sciences, Chemistry, Biotechnology, or related field.
• 3–5 years of experience in pharmaceutical manufacturing or validation, with a focus on cleaning validation.
• Strong knowledge of GMP and cleaning validation principles.
• Excellent problem-solving, documentation, and communication skills.
• Ability to work independently and in cross-functional teams.
• Hands-on experience with injectable manufacturing processes is a plus.
• Lean or Six Sigma certification preferred.

Why Join Us?

Our site in Uppsala is a global center of excellence — home to hundreds of professionals working across R&D, manufacturing, and quality, 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 results, embrace learning, and bring positive energy. We combine initiative with teamwork and collaboration. Above all, we are passionate about doing something meaningful for patients and healthcare professionals.

With us, you have the ultimate opportunity to gain new and challenging work experience and create an unparalleled, direct impact.

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