CQV Engineer
Performs cGMP compliance-based services (commissioning, qualification, validation, consulting, etc.)
Additional Responsibilities
- Write C/Q/V documents following established standards and templates, including but not limited to the following:
- Commissioning Forms
- C/Q/V Protocols and Summary Reports
- Standard Operating Procedures
- Impact Assessments
- Specifications (URS/FRS/DDS)
- FATS/SATs
- Perform field/site activities including, but not limited to, the following:
- Attend and witness FATs and SATs as a representative of IPS clients.
- Execution of commissioning forms and witnessing of vendor start-up and testing.
- Execution of C/Q/V protocols.
- Walkdown and verification of system drawings (P&IDs, as-builts, etc.)
- Compile data and prepare reports for completed C/Q/V activities including ETOPs, protocol data packages, etc.
- Assist in deviation investigation and resolution of problems and issues encountered during field execution activities.
- Work with the Project Delivery department or CM for start-up and vendor testing. Witness and troubleshoot as required.
- Primary responsibilities include C/Q/V of equipment and systems, including CSV and automation, supporting pharmaceutical, biotech, and medical device industries.
- Read, understand and utilize the IPS Best Practices and SOPs for delivery of compliance services
Job Types: Full-time, Contract
Pay: $50.00 - $65.00 per hour
Schedule:
- 8 hour shift
Education:
- Bachelor's (Required)
Location:
- Albany, NY 12244 (Preferred)
Ability to Commute:
- Albany, NY 12244 (Required)
Ability to Relocate:
- Albany, NY 12244: Relocate before starting work (Required)
Work Location: In person
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