IL ยท On-site
Project Commissioning (CQV) Manager - Pharmaceutical / Life Sciences ๐ Illinois, USA | Site-Based | Permanent We are supporting the appointment of a Project Commissioning (CQV) Manager for a major ...
IL ยท On-site
Project Commissioning (CQV) Manager - Pharmaceutical / Life Sciences ๐ Illinois, USA | Site-Based | Permanent We are supporting the appointment of a Project Commissioning (CQV) Manager for a major ...
IL ยท On-site
Project Commissioning (CQV) Manager - Pharmaceutical / Life Sciences ๐ 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 ...
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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 ...
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 ...
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 ...
Kenosha, WI ยท On-site
Arcadis is seeking a CQV PM to manage the entire program for our client in Wisconsin. Role accountabilities: โข Refine Program Level Strategy for assigned workstream โข Develop detailed activity ...
Kenosha, WI ยท On-site
Arcadis is seeking a CQV PM to manage the entire program for our client in Wisconsin. Role accountabilities: โข Refine Program Level Strategy for assigned workstream โข Develop detailed activity ...
Cranbury, NJ ยท On-site
Job Title - Manager - SR Manager, CQV Quality Control Work Location - Cranbuy NJ Job Summary The Manager, CQV Quality Control is responsible for the strategic and operational leadership of QC CQV ...
Cranbury, NJ ยท On-site
Job Title - Manager - SR Manager, CQV Quality Control Work Location - Cranbuy NJ Job Summary The Manager, CQV Quality Control is responsible for the strategic and operational leadership of QC CQV ...
Philadelphia, PA ยท On-site
Coordinate system walkdowns, punch list management, and turnover documentation activities * Ensure all CQV activities comply with FDA, cGMP, GDP, and company quality standards * Collaborate with ...
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Philadelphia, PA ยท On-site
Coordinate system walkdowns, punch list management, and turnover documentation activities * Ensure all CQV activities comply with FDA, cGMP, GDP, and company quality standards * Collaborate with ...
Raleigh, NC ยท On-site
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 ...
Raleigh, NC ยท On-site
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 ...
We are seeking an experienced Senior CQV Project Manager to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives.
Quick apply
We are seeking an experienced Senior CQV Project Manager to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives.
We are seeking an experienced Senior CQV Project Manager to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives.
We are seeking an experienced Senior CQV Project Manager to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives.
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.
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 ...
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 ...
Bend, OR ยท On-site
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 ...
Bend, OR ยท On-site
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 ...
Lexington, KY ยท On-site
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 ...
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Lexington, KY ยท On-site
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 ...
Raleigh, NC ยท On-site
Schedule Development & Management * Create and manage detailed CQV schedules using Primavera P6 and MS Project. * Break down all systems and equipment into System Boundary/Turnover Packages.
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Raleigh, NC ยท On-site
Schedule Development & Management * Create and manage detailed CQV schedules using Primavera P6 and MS Project. * Break down all systems and equipment into System Boundary/Turnover Packages.
$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 ...
$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 ...
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 ...
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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 ...
West Valley City, UT ยท On-site
CQV Engineer Location : West Valley City, Utah Duration : Long Term Position Overview We are ... Familiarity with validation documentation, protocol execution, deviation management, CAPA, change ...
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West Valley City, UT ยท On-site
CQV Engineer Location : West Valley City, Utah Duration : Long Term Position Overview We are ... Familiarity with validation documentation, protocol execution, deviation management, CAPA, change ...
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.
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.
$23K - $30.2K
4% of jobs
$30.2K - $37.5K
10% of jobs
$43.3K is the 25th percentile. Wages below this are outliers.
$37.5K - $44.7K
14% of jobs
$44.7K - $51.9K
16% of jobs
The median wage is $58.1K / yr.
$51.9K - $59.1K
7% of jobs
$59.1K - $66.4K
10% of jobs
$70K is the 75th percentile. Wages above this are outliers.
$66.4K - $73.6K
29% of jobs
$73.6K - $80.8K
4% of jobs
$80.8K - $88K
3% of jobs
$88K - $95.3K
1% of jobs
$95.3K - $102.5K
2% of jobs
$23K
$61.4K
$102.5K
Cities with the most Cqv Manager job openings:
States with the most job openings for Cqv Manager jobs include:
The top searched job categories for Cqv Manager jobs are:

IL โข On-site
Other
This job post hasย expired 2 days ago.ย Applications are no longer accepted.
Project Commissioning (CQV) Manager โ Pharmaceutical / Life Sciences
๐ 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:
โข Developing the overall Commissioning Execution Plan, strategy and methodology
โข Establishing commissioning philosophies, procedures and technical documentation
โข Integrating commissioning activities and milestones into the overall project schedule
โข Leading commissioning planning, scheduling and resource requirements
โข Coordinating Engineering, Procurement, Construction, Quality/CQV and HSE teams
โข Managing commissioning contractors, subcontractors and equipment vendors
โข Leading commissioning readiness reviews and system turnover activities
โข Overseeing Mechanical Completion, Systems Completion, pre-commissioning and startup
โข Managing functional testing, system acceptance and operational readiness
โข Supporting pharmaceutical CQV and GMP requirements
โข Managing client interfaces and commissioning-related stakeholder relationships
โข Monitoring commissioning KPIs, progress, risk, cost and schedule
โข Leading final turnover, handover and project closeout
โข Building, coaching and leading a multidisciplinary commissioning team
What Weโre Looking For
Candidates should ideally have:
โข 10+ years of Commissioning / CQV Management experience within complex capital projects
โข Significant Pharmaceutical / Biopharma / Life Sciences project experience
โข Strong understanding of GMP/cGMP and CQV environments
โข Experience leading commissioning on major EPC, EPCM, General Contractor or design-build projects
โข Multidisciplinary commissioning experience covering Mechanical, Electrical and Process systems
โข Demonstrable responsibility for commissioning teams, contractors and vendors
โข Experience taking systems from construction completion through startup and handover
โข Strong commissioning planning, scheduling and documentation experience
โข 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.