CQ Documentation Engineer - Germany, Frankfurt - 12 Month ContractLooking to take your career to the next level? We’re recruiting for a high-impact pharmaceutical project located near Frankfurt. With major capital investment experience driving various facility build projects. This is a unique opportunity for a CQ Documentation Engineer to join a global leader in the life sciences market and play a key role in shaping the future of advanced manufacturing.
Responsibilities include:
- Coordinate with Document Preparation Lead on deliverables and approvals using the Document Generation Tracker to manage milestones and timelines.
- Oversee Verification Design deliverables (EDR/DQ) and review/approve vendor documentation.
- Manage documentation for Factory Acceptance Testing (FAT).
- Support protocol development (FAT/IV/SAT/FV) with the Document Preparation Lead.
- Liaise with vendors to ensure GEP/GDP compliance for test documentation.
Key requirements include:
- Prepare CSRs (Commissioning Summary Reports) for executed documentation
- Ensure all the requirements for the IOQ summary reports are available and the good engineering and documentation practices have been followed throughout.
- Review all vendor and site change controls for impact to the completed testing as required.
- Generate Project specific SOP's / other documentation as applicable
- Support CQV and QA programmes as required
Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-CO1