We place validation specialists for projects in:
- Pharmaceutical Manufacturing – Validating production processes, utility systems (HVAC, water-for-injection), and cleaning procedures in GMP drug manufacturing facilities to comply with FDA and EMA regulations.
- Biotechnology & Biopharma – Qualifying bioreactors, lab equipment, and new processes in biotech R&D and production (cell culture, fermentation), ensuring robust results and audit-ready documentation.
- Medical Devices & Diagnostics – Executing equipment qualifications and sterilisation validation for medical device assembly lines and diagnostic product manufacturing, meeting ISO 13485 and FDA quality standards.
Why work with us?
At QCS Staffing, we understand what it takes to succeed in validation. Our specialist consultants know the technical qualifications (engineering degrees, Six Sigma, CQV certifications) and regulatory standards (cGMP, FDA, MHRA) that top employers expect. We work with leading global pharmaceutical and biotech companies—often giving you access to exclusive CQV contract opportunities across the US, Europe and beyond. From quick onboarding to tailored project matches, we connect you with roles that move your career forward. Let us help you land your next contract.
