Job Description
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: Head of Quality
Location: Uppsala, Sweden
About the Role
We are seeking an experienced and inspirational Head of Quality to lead and transform our Quality function at our site in Uppsala, Sweden This is a critical leadership role where you will shape a proactive, patient-focused, and risk-aware quality culture within a highly regulated pharmaceutical/biotech environment
As a key member of the leadership team, you will ensure full compliance with global regulatory standards while driving operational excellence, continuous improvement, and integration of quality across all phases of product development and manufacturing.
Key Responsibilities
- Lead the site’s Quality strategy, governance, and execution, ensuring full compliance with GMP/cGMP and international regulations
- Act as the primary Quality authority during regulatory inspections(e.g., EMA, FDA and other global agencies)
- Oversee and continuously improve the Quality Management System (QMS)covering QA, QC, validation, and regulatory compliance
- Ensure the approval and release of raw materials, packaging, intermediates, and finished products
- Drive management of deviations, CAPAs, change controls, and customer complaints
- Own supplier quality management, audits, and qualification processes
- Lead internal and external auditsand ensure inspection readiness at all times
- Oversee analytical, microbiological, and product quality control activities
- Ensure compliance with marketing authorizations and regulatory submissions
- Lead validation and qualification activities(equipment, systems, processes, computerized systems)
- Build and lead a high-performing Quality organization, including hiring, development, and performance management
- Define and manage Quality budgets and resources
- Contribute to site strategy and business planningas a key member of the Management Team
- Embed Health, Safety & Environment (HSE)principles into all quality-related activities
What We’re Looking For
Required Experience
- Mandatory:Extensive experience in pharmaceutical and/or biotechnology environments
- 10–15+ years of progressive experience in Quality (QA/QC)with significant leadership responsibility
- Proven track record managing regulated manufacturing environments
Education
- Bachelor’s or Master’s degree in a scientific discipline(e.g., Chemistry, Biochemistry, Microbiology, Chemical Engineering)
Technical Expertise
- Deep knowledge of GMP/cGMP regulations (EMA, FDA, ICH)
- Strong experience with regulatory inspections and audits (FDA/EMA)
- Expertise in QMS, validation, and regulatory compliance
- Solid understanding of product lifecycle and regulatory submissions
- Experience in project management and change management
Leadership Skills
- Strategic and hands-on leader with the ability to drive cultural transformation
- Strong stakeholder management and communication skills
- Ability to lead through complexity in a high-growth, high-regulation environment
Languages
- Fluent in English(written and spoken)
Why Join Us?
- Be part of a mission-driven organizationin the pharma/biotech space
- Lead impactful transformation in a high-visibility leadership role
- Work in Uppsala, a leading European hub for life sciences innovation
- Shape the future of quality in a growing and collaborative environment
Ready to Make an Impact?
If you are a quality leader passionate about excellence, compliance, and continuous improvement in Pharma/Biotech, we’d love to hear from you.