CQV Engineer
Job in
Cambridge, Middlesex County, Massachusetts, 02140, USA
Listed on 2026-02-12
Listing for:
Intellectt Inc
Full Time
position Listed on 2026-02-12
Job specializations:
-
Engineering
Validation Engineer, Pharma Engineer, Quality Engineering -
Pharmaceutical
Validation Engineer, Pharma Engineer, Pharmaceutical Manufacturing, Quality Engineering
Job Description & How to Apply Below
We are seeking a CQV Engineer with 3+ years of pharmaceutical industry experience to support commissioning, qualification, and validation activities for GMP manufacturing systems and equipment.
Key Responsibilities- Execute IQ, OQ, and PQ for pharmaceutical equipment, utilities, and facilities.
- Prepare and review validation documents (URS, protocols, and reports).
- Perform risk assessments and ensure compliance with cGMP and FDA regulations.
- Support deviations, change controls, and audits.
- Collaborate with Engineering, QA, and Manufacturing teams.
- Bachelor’s degree in Engineering or Life Sciences.
- 3+ years of CQV/Validation experience in the pharmaceutical industry.
- Knowledge of cGMP and FDA regulations (21 CFR Parts 210/211).
- Strong documentation and communication skills.
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×