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.
Looking for real growth in a dynamic, science-driven environment?
We’re growing our CQV team at Galderma Uppsala and offer exciting opportunities in validation and engineering.
About Galderma
Galderma is the world’s largest independent dermatology company, operating in nearly 90 countries with a portfolio that includes some of the most trusted brands in aesthetics and dermatological care — such as Restylane, Azzalure, and Sculptra.
At our Uppsala site, we offer something unique: the entire value chain — from R&D to manufacturing and global distribution — all in one location. This enables close collaboration, real impact, and rapid innovation.
We are now expanding our CQV (Commissioning, Qualification & Verification) team with an experienced engineer who is ready to grow with us, contribute to quality outcomes, and support our mission to deliver safe and effective dermatological solutions to patients worldwide.
About the Role
As a CQV Engineer, you will be responsible for qualifying and verifying critical manufacturing and utility systems in accordance with GxP standards and internal requirements. You will ensure that systems are designed, installed, tested, and maintained according to regulatory expectations and project timelines.
Key responsibilities include:
- Planning and executing Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for GxP systems.
- Writing, executing, and reviewing qualification protocols and reports.
- Providing support during deviations, change control, and CAPA activities.
- Collaborating closely with production, quality, engineering, and maintenance teams.
- Ensuring all activities follow applicable guidelines such as ASTM E2500, ISPE Commissioning and Qualification Good Practice Guide, and internal SOPs.
- Supporting requalification of systems and continuous improvement of CQV documentation and strategy.
This is a hands-on, on-site role in Uppsala due to the physical access required to systems and equipment.
Required Qualifications and Experience
- 2–5 years of experience in CQV, validation, or engineering within the pharmaceutical or medical device industry.
- Experience with executing and reviewing IQ/OQ/PQ protocols and working under cGMP conditions.
- Familiarity with qualification of cleanrooms, WFI systems, HVAC, gas utilities, cold storage, and aseptic manufacturing equipment.
- Strong knowledge of applicable regulatory frameworks and industry best practices.
- Fluent in both Swedish and English.
Preferred Qualifications
- Experience with computerized system validation (CSV).
- Familiarity with digital validation systems (e.g., ValGenesis, Veeva Vault).
- Experience with serialization, automation systems, or MES platforms such as Pas-X.
- Background in startup or large-scale production environments.
- Enjoyment of structured documentation work and detail-oriented tasks.
What We Offer
- A dynamic, cross-functional working environment with exposure to multiple technologies.
- Access to the full product lifecycle in a single location – from research and development to final manufacturing.
- A collaborative, inclusive culture that values every voice.
- Opportunities for professional growth, internal mobility, and training.
- Competitive salary and comprehensive benefits package.
Why Join Galderma?
At Galderma, you’ll have the opportunity to work with world-leading products and technologies in a company that puts science, quality, and patient outcomes first. You’ll join a supportive team of professionals who share a common goal — advancing dermatology for every skin story.
Our Uppsala site offers a rare opportunity to be involved in all stages of product development and manufacturing in one of the world’s most respected dermatology companies.
