Senior CQV Engineer
3 weeks ago
About IPS-Integrated Project Services, LLC
We are a global leader in developing innovative business solutions for the biotechnology and pharmaceutical industries.
As a Commissioning and Qualification (C/Q) professional with our team, you will perform cGMP compliance-based services, including commissioning, qualification, validation, consulting, and other related activities.
You will be responsible for writing and executing C/Q documents, performing field/site activities, collaborating with project delivery teams, and ensuring the successful completion of projects.
Main Responsibilities:
- Write and execute C/Q documents, including commissioning forms, protocols, and summary reports.
- Perform field/site activities, including attending Factory Acceptance Tests (FATs) and Site Acceptance Tests (SATs), execution of commissioning forms, and witnessing vendor start-up and testing.
- Compile data and prepare reports for completed C/Q activities.
- Assist in deviation investigation and resolution of problems and issues encountered during field execution activities.
Requirements:
- Bachelor of Science in Engineering or related field.
- 5 or more years of relevant experience in C/Q, pharmaceutical, biotech, medical device design, construction, commissioning, validation, or QA.
Benefits:
- A competitive salary range of $90,000 to $130,000 based on location and experience.
- An opportunity to work with a talented team of professionals.
- Ongoing training and development opportunities.
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