Job Title: CQV Engineer (Contract/Freelance)
Location: Geel, Belgium
Employment Type: Full-time (3–4 days onsite, 1–2 days remote)
Overview:
Our client, a leading pharmaceutical manufacturer, is seeking experienced CQV Engineers to support ongoing and upcoming projects at their API site in Geel. With a strong pipeline of 80–100 projects annually, this is an opportunity to join a high-performing team delivering critical qualification and validation activities for complex process systems.
Why this role exists:
Due to a continuous flow of projects and the need for qualified professionals to support equipment and system qualification activities, the team is expanding. If you bring the right expertise and mindset, there’s always room for you to contribute.
Key Responsibilities:
* Prepare and execute qualification protocols (IQ, OQ, PQ) for process equipment, including:
* Reactors (glass-lined or stainless steel)
* Centrifuges
* Dryers (vacuum, tray, rotary, or fluid bed)
* Vessels and tanks
* Process and utility piping systems
* Review and approve vendor FAT/SAT documentation and ensure traceability in site qualification packages.
* Oversee or perform testing, calibration, and verification of control systems and instrumentation.
* Ensure qualification documentation meets site and GMP standards.
* Manage deviations, non-conformances, and CAPAs related to qualification activities.
Requirements:
* 5–15 years’ experience in CQV or equipment qualification within the pharmaceutical industry.
* Strong understanding of GMP and equipment qualification processes.
* API site experience preferred (chemical processes rather than sterile manufacturing).
* Dutch language preferred; strong English speakers considered.
* Must be located within commuting distance of Geel.
Offer:
* Long-term freelance assignment with an industry leader.
* Hybrid working model (onsite & remote).
* Start date: ASAP this quarter.
* Competitive hourly rate (depending on experience).