CQV Engineer I

PM Group • Rahway, NJ

2h

About The Position

The CQV Engineer I is an entry-level role on PM Group’s growing Outsourced Technical Services team in Rahway, New Jersey. The role combines client interaction with technical work and is suited to someone with a basic understanding of commissioning, qualification, and validation (CQV) who wants to develop knowledge of the design-build industry. The engineer will be mentored by senior CQV team members and assist with developing validation protocols, qualification testing, and commissioning verification documents. The role involves learning and applying Current Good Engineering Practices and Current Good Manufacturing Practices to equipment, system, and facility qualifications in the pharmaceutical and biotechnology industries. Projects may cover new and existing equipment, systems, and facilities, with project sizes and scopes varying across the regulated life sciences industry.

PM Group is an employee-owned international project delivery firm with more than 4,000 people and over 50 years of industry experience. It serves clients in the pharmaceutical, food, biotech, medical technology, and mission-critical sectors. Its Outsourced Technical Services team provides technical professionals to complement client project teams.

Requirements

• 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.
• Ability to travel as needed for client and project development.
• Strong writing and documentation skills.
• Computer literacy and good experience using Microsoft Word and Excel.

Nice To Haves

• Previous co-op or internship experience in the pharmaceutical industry.

Responsibilities

• Perform work in compliance with PM Group’s Service Delivery Platforms and Quality Management System.
• Coordinate activities by communicating with the CQV department, other departments, project team members, clients, and external parties.
• Liaise with senior colleagues and mentors as appropriate.
• Keep abreast of current technology, regulatory requirements, and industry standards.
• Demonstrate knowledge of PM Group and industry-standard CQV and GMP methodologies and tools.
• Under supervision, prepare technical documents to agreed schedules and report progress in a timely manner.
• Under supervision, perform commissioning, qualification, and validation testing to agreed schedules and report progress in a timely manner.
• Carry out site visits and site surveys under supervision.
• Participate in Factory Acceptance Tests (FAT) and Site Acceptance Tests (SAT).
• Complete special projects as required.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level