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PM Group

CQV Engineer I

Rahway, NJ, United States

$75,000 to $90,000 USD / year

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Job details

Pay: $75,000 to $90,000 USD / year
Experience: 0-3 years of experience in computer system validation, laboratory systems, quality control, IT, automation, or pharmaceutical manufacturing support.
Posting language: English
Posted: Nov 9, 2026

Original job description

Overview

The CQV Engineer I position is an exciting opportunity to join PM Group’s quickly growing Outsourced Technical Services(OTS) team out of Rahway, NJ. Outsourced Technical Services (OTS) is an integral part of PM Group’s ability to support clients across the complete project life cycle. We have over 50 years’ industry experience, strong technical knowledge and integrated resources. Clients look to us to provide experienced technical professionals that complement their project teams. Together we are sharing knowledge, learning, growing and continuing to be an integral part of supporting PM Group’s ongoing expansion in the US.

This is an entry-level career position and we are looking for a CQV Engineer who enjoys client interaction as well as the technical aspects of the position. This individual needs to have a basic understanding of the technical aspects of CQV with a desire to learn the nuances of the design build industry. The ability to successfully handle multiple real-time complex projects, maintain a strong work ethic and drive to deliver for clients as a collaborative colleague are necessary for this role. The Graduate CQV Engineer will be mentored by more senior level CQV team members and will assist with the development of documents for Validation Protocols, Qualification Testing, and Commissioning Verifications. The Graduate CQV Engineer will learn and implement Current Good Engineering Practices, and Current Good Manufacturing Practices as they apply to equipment, system, and facility qualifications in the pharmaceutical and bio-tech industries. Expect project work to include all levels of qualification document development and qualification testing performance. Project sizes and scopes will vary within the compliance regulated life science industry, focusing on both new and existing equipment, systems, and facilities.

PM Group is an employee owned, international project delivery firm with a team of 4,000+ 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 partners.

Responsibilities

Perform work in compliance with PM Group’s Service Delivery Platforms and Quality Management System
Interact and communicate with the CQV department, other departments, project team members, clients and other external parties to ensure co-ordination of activities
Liaise with senior colleagues and mentors as appropriate
Keep abreast of current technology, regulatory and industry standards
Demonstrate a knowledge of PM Group and / industry standard methodologies and tools for CQV and GMP
Under supervision, prepares technical documents in accordance with agreed schedules and reports progress in a timely fashion to avoid any undue delays
Under supervision, perform Commissioning, Qualification and Validation testing in accordance with agreed schedules and reports progress in a timely fashion to avoid any undue delays
Carries out site visits / site surveys, under supervision
Participates in Factory Acceptance Tests ( FAT ) and Site Acceptance Tests ( SAT )
Special projects as required

Qualifications

Bachelor’s degree in Engineering or Science
0-3 years of experience in computer system validation, laboratory systems, quality control, IT, automation, or pharmaceutical manufacturing support.
Previous Co-op or Internship with pharmaceutical industry experience is preferred
The ability to travel as needed for client and project development
Strong writing and documentation skills
Computer literate with good experience working within MS Word and Excel

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 2026 business strategy. Click here to read more in our 2025 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.

PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.

Pay Range Disclosure:

The pay range for this position is $75,000 – $90,000 annually. This range represents the base salary that PM Group reasonably expects to pay for this role at the time of posting. The actual compensation offered will depend on factors such as work location, qualifications, skills, and relevant experience.

RECRUITMENT AGENCIES NEED NOT APPLY

Perform work in compliance with PM Group’s Service Delivery Platforms and Quality Management System
Interact and communicate with the CQV department, other departments, project team members, clients and other external parties to ensure co-ordination of activities
Liaise with senior colleagues and mentors as appropriate
Keep abreast of current technology, regulatory and industry standards
Demonstrate a knowledge of PM Group and / industry standard methodologies and tools for CQV and GMP
Under supervision, prepares technical documents in accordance with agreed schedules and reports progress in a timely fashion to avoid any undue delays
Under supervision, perform Commissioning, Qualification and Validation testing in accordance with agreed schedules and reports progress in a timely fashion to avoid any undue delays
Carries out site visits / site surveys, under supervision
Participates in Factory Acceptance Tests ( FAT ) and Site Acceptance Tests ( SAT )
Special projects as required
Bachelor’s degree in Engineering or Science
0-3 years of experience in computer system validation, laboratory systems, quality control, IT, automation, or pharmaceutical manufacturing support.
Previous Co-op or Internship with pharmaceutical industry experience is preferred
The ability to travel as needed for client and project development
Strong writing and documentation skills
Computer literate with good experience working within MS Word and Excel

Pay Range Disclosure:

RECRUITMENT AGENCIES NEED NOT APPLY

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More about this job

Skills

Good manufacturing practices
Regulatory compliance
Quality assurance procedures
Quality control
Pharmaceutical processes
Pharmaceutical industry
Documentation
Computer skills
Microsoft Word
Microsoft Excel

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