Experienced C&Q Process Engineer

Publiceringsdatum: 2025-05-15

Letar du efter ett jobb inom yrken med teknisk inriktning? Det är nu möjligt för dig att få jobb som processingenjör, kemiteknik hos Q-Med AB. Om du vill arbeta heltid hos Q-Med AB, har de just nu en tjänst tills vidare som kan passa dig.

Denna position är tillgänglig i Uppsala. Företaget Q-Med AB erbjuder just nu spännande karriärmöjligheter. Om du vill jobba som processingenjör, kemiteknik har de nu ett ledigt jobb - kolla in annonsen för att se om du har rätt erfarenhet. Bli en del av teamet hos Q-Med AB som processingenjör, kemiteknik genom att ansöka senast söndag den tjugofemte maj 2025.

Jobbannons

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.

Application Process

Apply via our careers page on galderma.com, or, if you're already employed at Galderma, through the internal Workday platform.

Application deadline: April 30, 2025.

We evaluate candidates on an ongoing basis and may fill the role before the deadline.

Ready to be part of something meaningful?

Apply now and help us shape the future of dermatology - one qualified system at a time.