Overview
On Site
Full Time
Skills
Change Control
Technical Support
Manufacturing
Documentation
Corrective And Preventive Action
Job Details
Roles & Responsibilities:
- Minimum 7 years of CQV experience in a parenteral fill/finish environment.
- Lead process validation projects of broad scope.
- Responsible for project deliverables such as VMPs, pFMEAs, PPQ protocols and reports, change control assessments, technical transfer assessments, as well as other client deliverables as required.
- Provide technical support to Manufacturing - troubleshooting and resolving process related issues.
- Participate in investigations and provide documentation for Deviations and CAPA based on OOS/OOT results or validation activities.
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