CQV Upstream/Downstream Leiden

CQV Upstream/Downstream Expert - Leiden, Netherlands - 12+ Months Contract

We're hiring a hands-on Upstream or Downstream Expert for a long-term contract with a leading biopharma company in Leiden. This is a great opportunity to join a high-performing team and work on a cutting-edge biologics manufacturing project.

Location: Leiden, Netherlands

Duration: 12+ Months

Start: ASAP

Type: Freelance Contract

Key Responsibilities:

• Execute Upstream (cell culture, bioreactors) or Downstream (chromatography, TFF, filtration) operations in a GMP setting
• Operate equipment like bioreactors, AKTA systems, TFF skids, and perform in-process controls
• Support CQV: IQ/OQ/PQ execution, cleaning validation, tech transfer, and process qualification
• Accurately document activities (batch records, deviations, CAPAs)
• Collaborate with QA, Engineering, and MSAT to ensure compliance and continuous improvement

Requirements:

• 3-5+ years in GMP biopharma manufacturing (USP or DSP)
• Strong experience with process equipment, validation, and troubleshooting
• CQV knowledge and hands-on validation protocol execution
• Solid documentation and regulatory compliance skills

Apply now: Send your CV to for immediate feedback!