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Job Description:
Performs cGMP compliance-based services (commissioning, qualification, validation, consulting, etc.) as developed and defined in project agreements with IPS’ clients. Follows IPS and client standards and requirements, overall good industry practices for C/Q/V services and regulatory requirements. May also perform standalone commissioning services for non-FDA regulated clients.
KEY ACTIVITIES AND RESPONSIBILITIES
- Write C/Q/V documents following established standards and templates, including but not limited to the following:
- Commissioning Forms
