Validation Engineer

CAI; Princeton (NJ); On-site; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking CQV Engineers to join their dynamic team in Princeton. This role involves developing critical documentation for commissioning, qualifications, and validation processes in regulated environments. Ideal candidates will have 2-4 years of experience and a strong foundation in pharmaceutical manufacturing processes. The company offers a supportive environment with competitive compensation, benefits, and opportunities for professional growth. If you are driven, have a can-do attitude, and are ready to make a meaningful impact, this opportunity is perfect for you.

Benefits

15% retirement contribution

24 days PTO

5 sick days per year

Health insurance at low cost

Financial support for education

70% long term disability paid

Qualifications

• 2-4 years' experience in a regulated industry.
• Strong background in commissioning and qualification.

Responsibilities

• Develop documentation for Commissioning, Qualifications, and Validation.
• Responsible for protocol writing, execution, and field verification.

Skills

Commissioning

Qualification

Validation

Protocol Writing

Field Verification

Pharmaceutical Manufacturing Processes

Troubleshooting

Utilities Management (WFI, RO, HVAC)

Education

BS in Science or Engineering

Equivalent Experience

Job description

We are seeking CQV Engineers with 1-4 years' experience and we can assist with relocation costs.

Position Description:

The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These individuals are responsible for protocol writing and execution, field verification, and development of summary reports at the client site.

Requirements include:

Position Requirements:

1. BS in a science or engineering field or equivalent years of experience
2. Minimum 2-4 years' experience in commissioning and qualification in a regulated industry
3. Ideally, you will already have experience in 1 or more of the following: facilities and equipment startup, walk downs & troubleshooting, utilities (WFI, RO, HVAC) upstream, downstream, purification, recovery, building automation or other pharmaceutical manufacturing processes

Other Requirements:

1. Excellent oral and written English is required
2. Able to travel domestically and internationally if required
3. Able to work (paid) overtime
4. Able to work in the US without sponsorship now or any time or in the future

About CAI

CAI is a 100% employee-owned company established in 1996, that has grown year over year to more than 800 people worldwide. We provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA regulated and other mission critical industries.

Are You Ready?

Our approach is simple; we put the client’s interests first, we do not stop until it is right, and we will do whatever it takes to get there.

As owners of CAI, we are committed to living our Foundational Principles, both professionally and personally:

1. We act with integrity
2. We serve each other
3. We serve society
4. We work for our future

With employee ownership, one person’s success is everyone’s success; we work diligently to accomplish team goals. We place Team Before Self, demonstrate Respect for Others, and possess a can-do attitude. That is how we have grown exponentially.

Benefits

Our full-time positions offer competitive compensation and benefits which include: up to 15% retirement contribution, 24 days PTO and 5 sick days per year, health insurance at extremely low cost to employee, financial support for both internal and external professional education as well as 70% long term disability paid for by the company.

This job description is not all inclusive and you may be asked to do other duties. CAI will also consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of the Fair Chance Act (FCA) / Fair Chance Ordinance (FCO).