CQV Engineer II - Raleigh, NC

· Job Title: C&Q Engineer (Mid -Senior Level) Clean Utilities & Downstream Equipment · Location: Greater Raleigh Area, NC  · Industry: Pharmaceutical Manufacturing · Employment Type: Full-Time or Contract · Position Summary: · We are looking for a mid- to senior-level Commissio ...

The C&Q Lead is responsible for directing and executing all commissioning activities for plant utility systems within our client's Expansion Project in Apex, NC.This role ensures all utility systems are designed, installed, tested, energized, and documented in accordance with pro ...

We are seeking a motivated and detail-oriented Entry-Level Equipment Validation Engineer to support Commissioning, Qualification, · and Validation (CQV) activities for GMP manufacturing · and utility equipment at a client site.A highly competitive benefits package including pre ...

The Commissioning Qualification and Validation Engineer II report directly to the Team Leader Manager or Director of the CQV Team depending on the organizational structure. · CQV Engineers take a proactive role in supporting CQV projects and in providing client support. They buil ...

We don't settle until we give our best and know that we're making a difference. As a Commissioning Qualification and Validation CQV Engineer you'll join our collaborative team providing CQV support to clients that manufacture GMP products on a consistent basis in conjunction with ...

CQV Engineer – Process & Utility Systems Our client is seeking a Senior Process & Mechanical Engineer with extensive experience in pharmaceutical GxP environments, specializing in utility systems... · ...

CQV Engineer<\/span> · <\/span><\/span><\/p> · Location - onsite Durham, NC<\/span> · <\/span><\/span><\/div> · <\/span><\/span><\/span><\/p> · New Grad role to be utilized as · needed for CQV/manufacturing support. On -the -Job training will be provided as · needed.<\/span> · < ...

· Position: CQV Engineer · Company Overview: · PharmEng Technology is a leading global provider of engineering and consulting services to the pharmaceutical and biotechnology industries. We specialize in providing innovative solutions to our clients to help them achieve their go ...

Experience Required: · 6+ years of CQV experience in GMP-regulated pharmaceutical or biotechnology manufacturing environments · Top Required Skills (Must-Have): · Commissioning, Qualification & Validation (CQV) lifecycle · Solution preparation systems (buffer prep, media prep, mi ...

We are hiring CQV Engineers (I, II, III, IV) of varying experience responsible for the commissioning, qualification and validation for facilities utilities and process equipment in the pharmaceutical and biotech industries. · ...

· CQV Engineer - Downstream Process Equipment (Biopharma) · Employment Type: Permanent/Contract (Fulltime) · We are seeking a skilled CQV Engineer to support commissioning and qualification activities for downstream process equipment within a large-scale biopharmaceutical manufa ...

The CQV Engineer is responsible for the planning, execution and documentation of commissioning qualification and validation activities for GMP equipment. · ...

Experience Required: · 6+ years of CQV experience in GMP-regulated pharmaceutical or biotechnology manufacturing environments · Top Required Skills (Must-Have): · Commissioning, Qualification & Validation (CQV) lifecycle · Downstream purification systems (chromatography, TFF, fil ...

Experience Required: · 6+ years of CQV experience in GMP-regulated pharmaceutical or biotechnology manufacturing environments · Top Required Skills (Must-Have): · Commissioning, Qualification & Validation (CQV) lifecycle · Solution preparation systems (buffer prep, media prep, mi ...

Experience Required: · 6+ years of CQV experience in GMP-regulated pharmaceutical or biotechnology manufacturing environments · Top Required Skills (Must-Have): · Commissioning, Qualification & Validation (CQV) lifecycle · Upstream bioprocess systems (bioreactors, media/buffer pr ...

We are seeking an experienced CQV Validation Engineer to join our team in Cary, NC. The ideal candidate will have a strong background in the pharmaceutical or biotech industry and 5–8 years of experience in commissioning, qualification, and validation of equipment, systems, and p ...

The CQV Engineer II report directly to the Team Leader, Manager, or Director of the CQV Team. These positions are exempt. Up to 100% travel may be required. · CQV Engineers take a proactive role in supporting CQV projects and in providing client support..Performs commissioning, q ...

The Commissioning, Qualification, and Validation Engineer II report directly to the Team Leader Manager or Director of the CQV Team depending on the organizational structure. Up to 100 travel may be required. · ...

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. · Our goal is to skyrocket our clients' success, a ...

Job Information · Date Opened · 02/27/2026 · Job Type · Full time · Work Experience · 10+ years · Industry · Pharma · City · Holly Springs · State/Province · North Carolina · Country · United States · Job Description · PSC Biotech provides the life sciences with essential service ...