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.
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.
Location: Uppsala
Employment type: Full-time
The Role
We are seeking a Quality Control Specialist – Analytical Methods, Protein to join our Quality Control (QC) organization. In this senior expert role, you will act as the technical authority in protein-based analytical methods, providing guidance, training, and scientific support to QC colleagues, cross-functional departments, and Galderma’s global network. You will ensure analytical methods and laboratory practices comply with GMP and internal quality standards, lead method validations, and drive continuous improvement and optimization within your area of expertise. This position offers an exciting opportunity for an experienced professional with deep technical knowledge and a passion for analytical excellence and quality.
Key Responsibilities
- Serve as Subject Matter Expert (SME) in analytical methods for proteins, including chromatographic, electrophoretic, and spectroscopic techniques.
- Provide technical leadership, training, and mentorship to QC analysts and cross-functional partners.
- Lead and coordinate method validations, including design, execution, evaluation, and reporting.
- Ensure analytical methods and QC operations comply with GMP, GxP, and Galderma quality standards.
- Identify, assess, and mitigate quality and compliance risks; support investigations with technical expertise.
- Represent QC in cross-functional and global projects, providing analytical insights and recommendations.
- Drive continuous improvement and simplification of analytical methods, work instructions, and quality systems.
- Prepare and present technical documentation and reports for audits, inspections, and internal/external stakeholders.
- Contribute to a positive, compliant, and collaborative laboratory culture.
Your Profile
Education:
- PhD or Master’s degree (or equivalent) in Biochemistry, Biotechnology, or a related field.
Experience:
- Minimum 10 years of experience in Quality Control or R&D with a focus on protein analytical methods.
- Extensive laboratory experience in chromatographic, electrophoretic, or spectroscopic analysis of proteins (e.g., SE, SEC-HPLC, SDS-PAGE, Western Blot).
- Strong knowledge of method development, optimization, and validation.
- Documented experience with GxP, GMP, and regulatory requirements for pharmaceuticals and/or medical devices.
- Proven ability to train, coach, and explain complex analytical concepts to internal and external audiences.
Skills:
- Advanced problem-solving and project management abilities.
- Strong communication and presentation skills in English and Swedish (both written and spoken) is a must.
- Ability to work independently and collaboratively in a global, cross-functional environment.
