Cleanroom Engineer - 19361

Assignment Description

We are looking for an experienced Cleanroom Engineer / Cleanroom Microbiologist

What You Will Work On

• Plan and execute Commissioning, Qualification & Validation (CQV) activities for cleanrooms
• Prepare and review CQV documentation, including:URS
• Risk assessments
• FAT/SAT protocols
• IQ/OQ/PQ protocols
• Validation reports

Participate in qualification of cleanrooms and HVAC systems

Support installation and commissioning of production equipment and technical systems

Coordinate and manage deviations related to qualification and validation

Ensure compliance with GMP and regulatory requirements

Coordinate CQV activities across multiple disciplines

Collaborate with QA, production, project management and external suppliers

Track activities and ensure project progress

Support qualification of process equipment and facility systems

Contribute to validation and quality assurance activities throughout the project

What You Bring

• Experience qualifying cleanrooms
• Experience qualifying HVAC systems
• Experience qualifying process equipment
• Experience with utilities, such as PW, WFI, compressed air and clean gases
• Strong knowledge of GMP and regulatory requirements
• Experience writing and reviewing qualification and validation documentation
• Strong understanding of CQV processes
• Strong technical understanding of cleanrooms and associated systems
• Experience working cross-functionally with different disciplines
• Strong coordination and project execution skills
• Ability to work independently and drive activities forward
• Very good communication skills in Swedish and English
• Strong quality-focused and structured approach

Interested? Please share your updated CV at cv@veritaz.se to proceed further.