Overview The CQV Engineer II position is an exciting opportunity to join PM Group’s quickly growing Southeast USA area team at a client site in Richmond, VA area. Together we will all be sharing knowledge, learning, growing and continuing to be an integral part of supporting PM Group’s ongoing expansion in the US. Our office is executing cutting-edge projects for Cell & Gene Therapy, Biologics, and Pharma facilities – from feasibility through to qualification – for both local and international clients. With our clients and partners, we will deliver projects that improve the everyday lives of people across the globe.
This is an early career position and we are looking for a professional who enjoys client interaction as well as the technical aspects of the position. This position requires an understanding of the technical aspects of commissioning (Cx), qualification and validation (CQV). The ability to successfully handle multiple real-time complex projects while maintaining a strong work ethic, and drive to deliver for clients, as a collaborative colleague, is necessary for this role. An understanding and applying the principals of good documentation practices (CGDP) is essential to performing in this position. The CQV Engineer II is mentored by more senior level CQV team members and will report to the Director of CQV. Their responsibilities will include document development as well as testing execution to meet client qualification needs. Expect project work to include all levels of qualification from design to completion. Project sizes will vary and the duties of the role require periotic travel to client sites.
PM Group is an employee owned, international project delivery firm with a team of 3,800+ people. We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organizations. We are focused on growing a sustainable business centered on our people, our clients and trade partner
Responsibilities - Performs work in compliance with PM Group’s Service Delivery Platforms and Quality Management System (QMS)
- Demonstrates an understanding of project scope of work assigned
- Demonstrates an understanding of commercial aspects (hours and capital cost) of their work
- Delivers scope of work within budgeted hours
- Document development as well as testing execution to meet client qualification needs
- Applying the principals of good documentation practices (CGDP)
- Collaborate in a multi discipline team environment
- Independently perform qualification protocols and review other team members qualification documents
- Ensure the implementation of current good manufacturing practices (CGMP)
- Special projects as assigned
Qualifications - Bachelor’s degree is required; an engineering degree is preferred
- 2 + Years of CQV experience in the Pharmaceutical, Biotech, Life Science and/or Cell & Gene Therapy industries
- Experience working with current good engineering and current good manufacturing practices
- Demonstrated experience working in an industry regulated life sciences environment
- Understanding of the entire validation life cycle and change control process
- Knowledge of cGMP Manufacturing environments is preferred
- Good technical reporting writing skills are mandatory
- The ability to travel as needed for client development and project execution
All of your information is confidential according to EEO guidelines.
Why PM Group?
As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2025 business strategy. Click here to read more in our 2024 Environmental, Social and Governance Report.
Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.
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