Upvote
Downvote
Senior Project Manager, CQV
Share Job
- Suggest Revision
Full-time
- In this role, you will perform cGMP compliance-based services (commissioning, qualification, validation, consulting, etc.)
- 10+ years of experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA.
- Project Management Professional (PMP) certification or a Professional Engineer (PE) license.
- General exposure and experience in a GMP/Validation discipline with a knowledge and understanding of pharmaceutical Design/Build/Commission/Validation processes and how they relate to regulatory requirements and cGMP regulations within the E.U. and U.S. FDA.
- The employee is designated for field work and attends activities at client sites where they work in construction, process, packaging, manufacturing, research, or other "non-administrative" areas.
Active Job
Updated 2 months agoSimilar Job
Relevance
Active