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
Join Galderma, a leading global dermatology company with a strong international presence and a commitment to innovation, collaboration, and excellence. We offer exciting opportunities for personal and professional development in a dynamic and purpose-driven environment.
About the Role
In this position, you will perform and review analytical testing according to established methods, using qualified instruments and working within agreed timelines. You will help ensure that methods and instructions are accurate and user-friendly, that instrument maintenance and calibrations are carried out as planned, and you will continuously contribute to improving analytical processes and workflows.
Key Responsibilities
Perform and review analytical tests according to SOPs using qualified instruments
Document all QC activities in line with established instructions
Contribute to process improvement and simplification initiatives
Report deviations and support investigations
Take responsibility for more complex methods, processes, and instruments according to certification
Conduct risk assessments related to methods and instruments
Update QC documents
Lead deviations and change control activities within your responsibility area
Support method validation and perform Class III instrument qualifications
Present relevant activities during audits
Contribute to a positive and collaborative working environment
Your Profile
Experience:
Bachelor’s degree or equivalent qualification in a relevant scientific field
2–5 years of experience in a QC laboratory or similar regulated environment
Documented GxP training and experience (pharmaceutical and/or medical device)
Experience with laboratory data systems, equipment qualification, and GxP-compliant testing
Experience performing or supporting method validation and/or instrument qualification
Experience preparing QC documentation and supporting audit readiness
Skills:
Strong understanding of GxP principles and how to ensure compliance
Solid knowledge of analytical laboratory techniques and data integrity requirements
Ability to explain analytical methods and procedures clearly to internal/external stakeholders
Strong documentation, analytical, and problem-solving skills
Ability to work independently with moderate supervision
Professional proficiency in English and Swedish, both written and spoken
Collaborative mindset and ability to contribute to a positive team atmosphere
Ability to perform delegated QC release of products, utilities, and incoming materials