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Business Analyst, Serialization & Traceability L3 Expert
AI Summary
Manages end-to-end validation activities for serialization and traceability IT systems in a GxP-regulated environment, ensuring systems remain validated throughout their lifecycle.
About this role
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.
Business Analyst, Serialization & Traceability L3 Expert
Location: Krakow, Poland, 4 days onsite from 2027
We are looking for an experienced Test Manager & Validation Lead to take ownership of validation activities across our serialization and wider IT landscape.
You will be responsible for ensuring our GxP systems are appropriately validated and remain in a validated state throughout their lifecycle. This is a hands-on role covering validation strategy, documentation, testing and close collaboration with IT, Quality, Compliance and business teams.
Key Responsibilities
- Define and manage end-to-end validation strategies and plans.
- Prepare and maintain validation documentation, including risk assessments, validation plans, functional and technical specification, test protocols, test execution reports and final validation reports.
- Coordinate and participate in test execution and review.
- Manage deviations, non-conformities and follow-up actions.
- Ensure systems remain in a validated state following changes and updates.
- Work closely with IT Compliance, Quality, business teams and technical colleagues.
- Support functional test scenarios and ensure appropriate test data is available.
- Provide validation expertise throughout implementation and operational activities.
Ideally you will have
- Strong expertise in GxP and Computerized System Validation.
- Hands-on experience preparing and managing validation documentation.
- Experience managing the full validation lifecycle for computerized systems.
- Strong understanding of testing, risk assessments, deviations and validation controls.
- Experience within pharmaceutical, life sciences or another highly regulated environment.
- Strong attention to detail and a structured approach to documentation.
- Able to manage validation activities independently from start to finish.
- Strong communication and collaboration skills across technical and business teams.
- Experience with serialization or traceability systems would be beneficial.
What we offer in return
We offer a competitive reward package, alongside benefits designed to support your health, wellbeing and development, including:
- Private healthcare and life insurance
- Pension plan
- Health and wellbeing benefits, including access to fitness support
- Annual leave and additional employee benefits
- Learning and development opportunities
- An international, collaborative environment where you are trusted to take ownership and make an impact
Why Join Us?
You’ll be joining a global dermatology leader with premium brands trusted worldwide and a team culture built on collaboration, accountability and care.
We believe diverse perspectives help us deliver better outcomes for our customers, patients and consumers. At Galderma, our people make a difference, and we want every team member to feel supported to thrive and do their best work.
Ready to make an impact?
Apply now and join us in shaping the future of dermatology.
Skills
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