Explore 1M+ Live Opportunities.
Direct applications, high-package MNC listings, and exclusive insider referrals updated daily across 50+ niches worldwide.
Live Jobs|Remote & Onsite|Apply in 1 Click
Join Our WhatsApp Job ChannelDirect applications, high-package MNC listings, and exclusive insider referrals updated daily across 50+ niches worldwide.
DPS Group Global · Cary, North Carolina
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
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
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 &
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
Ability to work independently and manage multiple priorities
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.
#LI-SM1
Details
| Company | DPS Group Global |
| Location | Cary, North Carolina |
| Type | FULL TIME |
| Niche | None |