CQV Engineer II

PM Group•Conshohocken, PA

About The Position

The CQV Engineer II is an early-career role on PM Group’s Outsourced Technical Services team in Indiana. The position combines client interaction with technical work involving commissioning, qualification, and validation (CQV). The engineer is expected to manage multiple complex projects, collaborate effectively, maintain a strong work ethic, and apply current good documentation practices (CGDP). The role is mentored by senior CQV team members and reports to the Director of CQV. Work includes developing documents and executing tests to meet client qualification needs, with project assignments spanning qualification from design through completion. The employee must be willing to travel to client sites in Indiana and as needed for client development and project execution. PM Group is an employee-owned international project delivery firm with more than 4,000 people, serving the pharmaceutical, food, biotech, medical technology, and mission-critical sectors. The company describes itself as focused on sustainable business, inclusion, diversity, and a workplace built on mutual respect and belonging. Reasonable accommodations are available to candidates with disabilities during recruitment.

Requirements

  • Bachelor’s degree required; an engineering degree is preferred.
  • 3–5 years of CQV experience in the pharmaceutical, biotech, life science, and/or cell and gene therapy industries.
  • Experience working with current good engineering practices and current good manufacturing practices.
  • Demonstrated experience working in a regulated life sciences environment.
  • Understanding of the entire validation life cycle and change control process.
  • Mandatory good technical report-writing skills.
  • Ability to travel as needed for client development and project execution, including travel to client sites in Indiana.
  • Ability to handle multiple complex projects while maintaining a strong work ethic and collaborating effectively.

Nice To Haves

  • Engineering degree preferred.
  • Knowledge of cGMP manufacturing environments preferred.

Responsibilities

  • Perform work in compliance with PM Group’s Service Delivery Platforms and Quality Management System (QMS).
  • Understand the assigned project scope of work.
  • Understand the commercial aspects of assigned work, including hours and capital cost.
  • Deliver assigned scope of work within budgeted hours.
  • Develop documents and execute testing to meet client qualification needs.
  • Apply the principles of current good documentation practices (CGDP).
  • Collaborate in a multidisciplinary team environment.
  • Independently perform qualification protocols and review qualification documents prepared by other team members.
  • Ensure implementation of current good manufacturing practices (CGMP).
  • Undertake special projects as assigned.
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