Senior CQV Engineer

3 weeks ago


Oceanside, California, United States IPS-Integrated Project Services, LLC Full time

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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