More jobs:
GMP CQV Validation Documentation Specialist
Job in
Fishers, Hamilton County, Indiana, 46085, USA
Listed on 2026-08-17
Listing for:
INCOG BioPharma Services
Full Time
position Listed on 2026-08-17
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist
Job Description & How to Apply Below
INCOG Bio Pharma 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-LjbffrTo View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×