INCOG BioPharma Services seeks a Validation Technical Writer to own CQV documentation within the Engineering and Technical Operations team. You will craft, revise, and organize GMP documentation, including SOPs, work instructions, and validation lifecycle records, ensuring audit readiness and regulatory compliance.
Preferred candidates have 3+ years of technical writing in regulated environments (or 1 year with validation/engineering exposure).
#J-18808-LjbffrGMP CQV Validation Documentation Specialist in fishers at Unknown Company
This position is listed as full time and onsite.