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Cqv Manager Jobs (NOW HIRING)

IL ยท On-site

Project Commissioning (CQV) Manager - Pharmaceutical / Life Sciences ๐Ÿ“ Illinois, USA | Site-Based | Permanent We are supporting the appointment of a Project Commissioning (CQV) Manager for a major ...

PR ยท On-site

This role is for Sr. CQV Manager/PM will require to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives. This ...

CQV Manager/PMwill require to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives. This individual will oversee ...

PR ยท On-site

This role is for Sr. CQV Manager/PM will require to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives. This ...

Arcadis is seeking a CQV PM to manage the entire program for our client in Wisconsin. Role accountabilities: โ€ข Refine Program Level Strategy for assigned workstream โ€ข Develop detailed activity ...

Develop and manage CQV schedules, ensuring alignment with project milestones * Support risk assessments and ensure compliance with regulatory expectations * Mentor and train junior engineers and ...

Manages multiple and complex CQV projects, collaboration with cross functional teams, provides status reports and coordinates with other departments or outside contractors/vendors to complete tasks.

Develop and manage CQV schedules, ensuring alignment with project milestones * Support risk assessments and ensure compliance with regulatory expectations * Mentor and train junior engineers and ...

Hiring Manager Notes * Immediate need due to a significant CQV validation backlog. * Strong preference for candidates with analytical laboratory experience. * Must be comfortable balancing priorities ...

Ability to work to project schedules and manage deliverables with timely, accurate reporting ... CQV experience with one or more of the following: formulation vessels, non-sterile nasal spray fill ...

CQV Lead

Davie, FL ยท On-site

$45 - $50/hr

CQV Lead Duration: 9 + months (possible extension) Davie, FL Shift Schedule: Monday - Friday 8.00AM ... Lifecycle & Compliance Management * Maintain validated state through lifecycle management, periodic ...

$79K - $104K/yr

Key Responsibilities Lead and manage a team of CQV engineers, contractors, and specialists in all commissioning and qualification activities. Oversee CQV activities for clean and black utility ...

CQV Engineer

Austin, TX ยท On-site

Ensure compliance with GMP, FDA regulations, cGMP guidelines, and internal quality management ... CQV), Equipment Qualification, or Validation Engineering within the pharmaceutical, biotechnology ...

Manages multiple and complex CQV projects, collaboration with cross functional teams, provides status reports and coordinates with other departments or outside contractors/vendors to complete tasks.

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How much do cqv manager jobs pay per year?

As of Sep 2, 2026, the average yearly pay for cqv manager in the United States is $61,351.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $69,000.00 per year, depending on experience, location, and employer.
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Infographic showing various Cqv Manager job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $61,351 per year, or $29.5 per hour.

Project Commissioning (CQV) Manager - Pharmaceutical / Life Sciences

TEC Group International

IL โ€ข On-site

Other

This job post hasย expired 1 day ago.ย Applications are no longer accepted.


Job description

Project Commissioning (CQV) Manager โ€“ Pharmaceutical / Life Sciences

๐Ÿ“ Illinois, USA | Site-Based | Permanent


We are supporting the appointment of a Project Commissioning (CQV) Manager for a major pharmaceutical capital project in Illinois.

This is a senior, site-based leadership position for an experienced commissioning professional who can take overall responsibility for the commissioning and CQV function on a complex EPC project, from early project planning through construction, startup, qualification and final handover.

This is not purely a validation role. We are looking for someone who combines strong hands-on commissioning leadership, pharmaceutical/CQV knowledge and major construction project experience.


The Role:

You will establish and lead the project commissioning organization and oversee commissioning activities throughout:

Preconstruction โ†’ Engineering โ†’ Procurement โ†’ Construction โ†’ Mechanical Completion โ†’ Pre-Commissioning โ†’ Startup โ†’ CQV โ†’ Turnover & Handover


Key responsibilities will include:

โ€ข Developing the overall Commissioning Execution Plan, strategy and methodology

โ€ข Establishing commissioning philosophies, procedures and technical documentation

โ€ข Integrating commissioning activities and milestones into the overall project schedule

โ€ข Leading commissioning planning, scheduling and resource requirements

โ€ข Coordinating Engineering, Procurement, Construction, Quality/CQV and HSE teams

โ€ข Managing commissioning contractors, subcontractors and equipment vendors

โ€ข Leading commissioning readiness reviews and system turnover activities

โ€ข Overseeing Mechanical Completion, Systems Completion, pre-commissioning and startup

โ€ข Managing functional testing, system acceptance and operational readiness

โ€ข Supporting pharmaceutical CQV and GMP requirements

โ€ข Managing client interfaces and commissioning-related stakeholder relationships

โ€ข Monitoring commissioning KPIs, progress, risk, cost and schedule

โ€ข Leading final turnover, handover and project closeout

โ€ข Building, coaching and leading a multidisciplinary commissioning team


What Weโ€™re Looking For

Candidates should ideally have:

โ€ข 10+ years of Commissioning / CQV Management experience within complex capital projects

โ€ข Significant Pharmaceutical / Biopharma / Life Sciences project experience

โ€ข Strong understanding of GMP/cGMP and CQV environments

โ€ข Experience leading commissioning on major EPC, EPCM, General Contractor or design-build projects

โ€ข Multidisciplinary commissioning experience covering Mechanical, Electrical and Process systems

โ€ข Demonstrable responsibility for commissioning teams, contractors and vendors

โ€ข Experience taking systems from construction completion through startup and handover

โ€ข Strong commissioning planning, scheduling and documentation experience

โ€ข Bachelor's or Master's degree in Mechanical, Electrical, Chemical Engineering or equivalent relevant experience


Relevant technical experience may include:

HVAC | Clean Utilities | WFI | Purified Water | Clean Steam | Compressed Air | Process Piping | Process Skids | CIP/SIP | Cleanrooms | Pharmaceutical Manufacturing Equipment | MV/LV | UPS | Generators | BMS/BAS | EMS | PLC/DCS/SCADA | Instrumentation & Controls

Experience with FAT/SAT, IQ/OQ/PQ, risk-based qualification, ASTM E2500, ISPE and/or GAMP would be particularly relevant.


Who This Will Suit

The strongest candidates will be people who can operate at both levels: develop the commissioning strategy and organisation at leadership level while remaining close enough to site execution to drive construction turnover, startup, qualification and handover.


This is a full-time site-based position in Illinois, so candidates must be willing and able to work on site for the duration of the assignment.