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Role Overview:
- Manage eQMS implementation projects for life sciences clients.
- Coordinate activities across configuration, data migration, validation, and go-live.
Key Responsibilities:
- Develop and execute validation documentation, including URS, risk assessments, and traceability matrices.
- Facilitate requirements gathering and translate business processes into system workflows.
- Support system testing, UAT, defect resolution, and post-implementation support.
Requirements:
- 4–8 years of experience in pharmaceutical, biotech, or medical device environments.
- Hands-on experience with QMS platforms like Veeva, MasterControl, or ZenQMS.
- Strong knowledge of GxP, data integrity, and 21 CFR Part 11.
Work Environment:
- Primarily remote with approximately monthly travel to Eastern Pennsylvania.
- Contract-to-hire engagement with potential for long-term growth.
Partner Company
The hiring partner company supports end-to-end Quality Management System implementations for life sciences clients. They offer a remote contract-to-hire opportunity with potential for long-term growth.