About this opportunity
DPS Group Global lists this CQV Engineer II opportunity in cary, North Carolina. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Our Cary, NC CQV team is growing and looking to add additional CQV Engineer II resources to the team.
In this role, you will lead commissioning, qualification, and validation (CQV) activities for pharmaceutical and biopharmaceutical facilities, utilities, and equipment. The ideal candidate will have a strong understanding of GEP, cGMP requirements, and CQV lifecycle execution.
This position requires the ability to independently develop and execute validation deliverables, collaborate with cross-functional teams, support project planning, and ensure compliant project delivery. The CQV Engineer II will work with minimal supervision, mentor junior team members, and play a key role in both field execution and documentation activities.
This role will be based in Cary, NC and candidates must be willing to travel for extended periods of time based on assigned projects.
Key Responsibilities
Develop, review, and execute CQV deliverables in accordance with project standards and regulatory requirements:
Commissioning test protocols and checklists
Qualification protocols (DQ/IQ/OQ/PQ)
Standard Operating Procedures (SOPs) and Work Instructions
Impact assessments and system risk evaluations
Specifications (URS, FRS, DDS, etc.)
FAT and SAT protocols and summary reports
Turnover packages and validation summary reports
Lead and execute field-based CQV activities:
Attend and support FATs and SATs as required
Perform protocol execution and troubleshooting
Conduct system walkdowns, punch listing, and redline updates
Support startup and commissioning activities
Identify and resolve issues during testing and coordinate retesting as needed
Provide guidance and mentorship to junior CQV engineers and team members
Support development and improvement of CQV processes, templates, and tools
Contribute to planning efforts, including estimating and resource loading as needed
Skills & Qualifications
Bachelor’s degree in Engineering (Chemical, Mechanical, Industrial, related field) or equivalent hands on experience
4–6 years of CQV, validation, or relevant engineering experience in a regulated industry (pharmaceutical, biotech, medical device, etc.)
cGMP regulations and FDA expectations
Good Engineering Practices (GEP)
Commissioning and qualification lifecycle
Proficient in Microsoft Word and Excel (data tracking, documentation, and reporting)
Experience with document management systems (e.g., Kneat, Veeva, or similar) preferred
Strong technical writing and documentation review skills
Ability to work independently and manage multiple priorities
Strong communication and stakeholder coordination skills
Detail-oriented with a structured and disciplined approach to work
Ability to travel based on project needs
Comfortable working in both office and field environments
Capable of operating independently while supporting team objectives
The Company
DPS Group, Inc. is proudly part of the Arcadis Group of Companies and is a global EPCM firm offering full-service solutions within the Life Sciences (pharmaceutical, biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and solar) industries. DPS is dedicated to delivering successful projects with a ‘client-first’ mentality and personal touch across a range of market sectors: Project and Program Management, Procurement, Design, Construction Management, Health and Safety Management, Commissioning, Qualification, and Start-up.
DPS Engineering Inc. is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. DPS does not discriminate in employment opportunities or practices on the basis of race, color, religion, gender, national origin, age, sexual orientation, gender identity, disability, veteran status or any other characteristic protected by country, regional or local law.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.