Vacant job

About the assignment

We are looking for an experienced CQV Engineer for assignments in Södertälje/Stockholm. You will work on projects where precision, traceability, and GMP compliance are crucial – from early design phases to a completed and validated facility.

Your responsibilities

• Planning and execution of IQ/OQ/PQ
• Development and review of validation plans, protocols, and reports
• FAT/SAT and commissioning of equipment and process systems
• Risk analysis (e.g., FMEA), requirements traceability, and GMP documentation
• Collaboration with process, automation, and quality functions
• Support to the project team in technical and regulatory matters

We are looking for someone who

• Has a relevant engineering degree and at least 5 years of experience in CQV/validation within the pharmaceutical or other GMP-regulated industries
• Thrives in technology-driven projects with high demands on quality and documentation
• Is structured, solution-oriented, and communicative
• Is fluent in Swedish and English, both spoken and written
• Has a thorough understanding of GMP and quality systems

We offer

• A flexible and secure work environment with collective agreements
• Assignments where your expertise makes a concrete difference
• Opportunities to work on technically advanced and quality-critical projects
• Focus on personal development and continuous learning