CQV Engineers – Autoclave / Part Washer / Lyophilizer
Contract: Full-time Freelance / Contract
Duration: Project-based
Start: Immediate
Project Type: Sterile Pharmaceutical Manufacturing
We are looking for specialist CQV Engineers with experience in sterilization and critical process equipment. This role supports qualification activities within a high-compliance sterile GMP facility.
Key Responsibilities
Execute IQ/OQ protocols for sterilization equipment
Qualify autoclaves, part washers, and freeze dryers / lyophilizers
Conduct system walkdowns and vendor testing
Support startup and commissioning
Update RTMs and qualification documentation
Ensure compliance with GMP standards
Requirements
Strong sterile pharma CQV experience
Hands-on experience with autoclaves and/or lyophilizers
Understanding of sterilization validation principles
Experience in GMP-regulated environments
Independent execution capability
If this opportunity aligns with your background, please send your CV to and I will contact you to discuss next steps.