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