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PM Group

International project delivery firm for facilities

CQV Engineer 3

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeOceanside, CA, USA$100k - $130k /yr

About the Job

Requirements

  • A bachelor's degree is required; an engineering degree is preferred.
  • Five to ten years of CQV experience in the pharmaceutical, life sciences, biotech, and/or cell and gene therapy industries.
  • Experience with factory acceptance testing (FAT) and site acceptance testing (SAT).
  • Proven experience developing commissioning pre-functional checklists (PFCs) and performing commissioning functional performance testing (FPT).
  • Experience working with current good engineering practices and current good manufacturing practices.
  • Understand client needs and assist with developing user requirements specifications (URS) and system impact analysis (SIA).
  • Demonstrated experience working in an industry-regulated life sciences environment.
  • Participate in the document approval process.
  • Understand the entire validation life cycle and change control process.
  • Experience reviewing vendor-supplied documents such as submittal sheets and turnover packages (TOPs).
  • Be familiar with and understand the basics of design drawings.
  • Have a full understanding of all commissioning, qualification, and validation (CQV) testing procedures.
  • Ability to document and execute cleaning validation procedures.
  • Knowledge of cGMP manufacturing environments is required.
  • Good technical report-writing skills are mandatory.
  • Ability to travel as needed for client development and project execution.

Responsibilities

  • Perform work in compliance with PM Group’s Service Delivery Platforms and Quality Management System (QMS).
  • Interact independently with clients to assess and continuously reassess their needs.
  • Perform quality gap analysis.
  • Author technical and scientific reports.
  • Understand the assigned project scope of work and its commercial aspects, including hours and capital cost.
  • Deliver the scope of work within budgeted hours.
  • Develop documentation and execute testing to meet client qualification needs.
  • Apply the principles of good documentation practices (CGDP).
  • Collaborate in a multidisciplinary team environment.
  • Perform qualification protocols and review other team members’ qualification documents.
  • Ensure implementation of current good manufacturing practices (cGMP).
  • Independently assess qualification needs for equipment, facilities, utilities, and systems.
  • Provide technical guidance to less-experienced CQV team members.
  • Perform special projects as assigned.

About the Company

PM Group

International project delivery firm for facilities

PM Group is a global project delivery firm focusing on architecture, engineering, construction management, and validation services. It designs and delivers complex facilities for sectors including pharmaceuticals and life sciences, advanced technology and data centers, food and agriculture, and energy. The company provides end-to-end project work—from initial design and engineering through construction management and validation—to ensure facilities meet rigorous industry standards. What sets PM Group apart is its employee-owned structure and its international footprint, with offices across Europe, Asia, and the United States, enabling it to coordinate multidisciplinary teams on large-scale projects worldwide. The company’s goal is to ensure safe, compliant, and efficient delivery of complex facilities for its clients, helping them bring critical infrastructure online on time and within scope.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Machelen, Belgium
Founded
1973

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