Lead Deviation & Investigation Writer - Aseptic Fill-Finish
Listed on 2026-10-06
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist -
Manufacturing / Production
Regulatory Compliance Specialist
Stark Pharma Solutions Inc. in Michigan seeks an experienced Deviation Writer/Investigation Writer to join our regulated manufacturing teams. The role centers on writing and investigating manufacturing deviations, with emphasis on aseptic fill-finish operations.
You will partner with QA, Manufacturing, Engineering, Validation, QC, and Operations to review records, perform root cause analysis, and develop CAPAs ensuring GMP compliance and quality system effectiveness.
The Lead Deviation & Investigation Writer
- Aseptic Fill-Finish position in the Bio & Pharmacology & Health, Other field is open for applications.
We invite applications for the Lead Deviation & Investigation Writer
- Aseptic Fill-Finish position located in Midland, MI, United States.
The following position is for a Lead Deviation & Investigation Writer
- Aseptic Fill-Finish with Stark Pharma Solutions Inc.
Our team is growing, and we are hiring a Lead Deviation & Investigation Writer
- Aseptic Fill-Finish in Midland, MI, United States.
(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).