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Cqv Consultant Jobs (NOW HIRING)

Zifo

Principal CQV Consultant

Cary, NC · Hybrid

We are seeking a CQV Subject Matter Expert with a dual mandate: (1) Business Development / PreSales ... Advise and guide onsite/remote validation consultants on qualification strategy, deviations, test ...

NNE AS

Advanced CQV Engineer - Clayton NC

Clayton, NC · On-site

As an Advanced CQV Consultant, you will lead commissioning, qualification, and validation activities across complex life sciences projects. Serving as a Project Quality Manager (PQM), you will drive ...

NNE Inc.

$150 - $200/hr

As an Advanced CQV Consultant, you will lead commissioning, qualification, and validation activities across complex life sciences projects. Serving as a Project Quality Manager (PQM), you will drive ...

NNE AS

Advanced CQV Engineer - Clayton NC

Clayton, NC · On-site

As an Advanced CQV Consultant, you are responsible for planning, executing, and delivering commissioning, qualification, and validation (CQV) activities for pharmaceutical, biotechnology, and life ...

Valspec

CQV Consultant - California

Oceanside, CA · On-site

$65 - $75/hr

Senior Validation Engineer (CQV) -- Equipment & Cleaning Validation Join a leading biopharmaceutical manufacturer in the San Diego area as a Senior Validation Engineer supporting equipment and ...

Valspec

CQV Consultant - California

San Diego, CA · On-site

$65 - $75/hr

Senior Validation Engineer (CQV) -- Equipment & Cleaning Validation Join a leading biopharmaceutical manufacturer in the San Diego area as a Senior Validation Engineer supporting equipment and ...

Pioneer GMP Consulting

CQV Engineer

Louisville, CO · On-site

The consultant will provide hands-on support for an established periodic-review and requalification program. This role requires an experienced CQV professional who can quickly integrate with the ...

MMR Consulting

PR · On-site

MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and ... This role is for Sr. CQV Manager/PM will require to lead commissioning, qualification, and ...

MMR Consulting

PR · On-site

MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and ... CQV Manager/PMwill require to lead commissioning, qualification, and validation activities for ...

MMR Consulting

PR · On-site

MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and ... This role is for Sr. CQV Manager/PM will require to lead commissioning, qualification, and ...

Stark Pharma Solutions Inc

CQV Engineer

Charlotte, NC · On-site

We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering ...

CRB

CQV Engineer III

Raleigh, NC · On-site

... Consulting solutions to the global life sciences and food and beverage industries. Our 1,200 ... The CQV Engineer II will develop and implement commissioning strategies, lead verification ...

CRB

CQV Engineer III

Raleigh, NC

... Consulting solutions to the global life sciences and food and beverage industries. Our 1,200 ... The CQV Engineer II will develop and implement commissioning strategies, lead verification ...

Inc. (Vti)

CQV Engineers - Los Angeles

Los Angeles, CA · On-site

$60 - $80/hr

... consulting with some of the biggest companies in the Life Sciences industry. We are looking for ... We need multiple CQV Engineers with CQV protocol execution experience to provide execution support ...

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Cqv Consultant information

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How much do cqv consultant jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for cqv consultant in the United States is $41.55, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $49.52 per hour, depending on experience, location, and employer.

What is the difference between Cqv Consultant vs Quality Assurance Analyst?

AspectCqv ConsultantQuality Assurance Analyst
Required CredentialsCertifications in quality management, industry-specific standardsCertifications in QA methodologies, testing tools
Work EnvironmentConsulting firms, client sites, corporate officesIn-house testing teams, software companies, manufacturing plants
Employer & Industry UsageUsed across industries for compliance and process improvementPrimarily in software, manufacturing, and healthcare sectors

While both roles focus on quality, a Cqv Consultant typically provides expert advice on quality management systems and compliance, often working across multiple clients. A Quality Assurance Analyst mainly conducts testing and inspections within a specific organization to ensure product or service quality. Understanding these differences helps in choosing the right career path or job search focus.

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Cqv Consultant jobs near you
Infographic showing various Cqv Consultant job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $86,430 per year, or $41.6 per hour.

US - CQV Consultant

Boston, MA • On-site

Resolute Workforce Solutions
See more jobs at Resolute Workforce Solutionsexternal

Full-time

Re-posted 17 days ago

Job description


Client: Brevitas Corp.
Our Global Company, Brevitas Corp., is dedicated to helping organizations achieve tangible results and lasting improvements via successful project delivery, continuous process improvement and effective management of change. We serve businesses in a wide range of industries including Pharmaceuticals, Food & Beverage, Chemicals, and Information Technology.
We are looking for highly motivated and energetic individual to join our team as a CQV Consultant in Boston area, MA.
This job is located in the United States and only candidates eligible to work in the US for any employer will be considered.
***Travel will be required.
By applying to this job your profile will be considered for upcoming roles within the next 1-6 months when opportunities do arise.
Responsibilities:
  • Write C/Q/V documents following established standards and templates, including but not limited to the following:
    • CQV Master Plans
    • Commissioning Forms
    • CQV Protocols and Summary Reports
    • Standard Operating Procedures
    • Impact Assessments
    • Specifications (URS/FRS/DDS)
    • FATs/SATs
  • Review various protocols, executed records and reports that are generated during commissioning (FAT or SAT), validation activities (IQ, OQ, PQ, PV) for process, equipment, facility and utility systems to ensure compliance with company quality policies and regulatory requirements.
  • Able to lead CQV efforts around biopharmaceutical manufacturing including CIP/SIP, fermentation and purification systems, supporting utilities clean steam and WFI compressed air
  • Provide technical assistance during investigations of process /equipment / cleaning / validation issues and aid in the resolution of validation deviations, protocol discrepancies and non-conformances
  • Provide compliance expertise and leadership for projects involving commissioning, qualification, and validation of process, equipment, facility, and utility systems.
  • Review technical and quality system documents such as SOPs, Change Control and Deviation Reports, Batch Production Records, Technical Manuals, P&IDs, construction, as-built, flow diagrams as they relate to validation principles and regulatory compliance issues.
  • Perform the role of Validation Representative in review of Change Control Requests (CCR's) and CAPA.
  • Compile data and prepare reports for completed CQV activities including ETOPs, protocol data packages, etc.
  • Assist in deviation investigation and resolution for problems and issues encountered during field execution activities.

Qualifications:
  • Bachelor's Degree in Engineering, preferably Chemical or Biotechnology
  • High level of familiarity with MS Office package (Project, PowerPoint, Excel, Word)
  • 3-4+ years of experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation or QA.
  • Experience in writing and execution of VMP, FQ, IQ, OQ and PQ forms and protocols for GMP Utilities, Equipment, Systems and Software.
  • Must have experience with qualifying clean utilities, HVAC System, Vaccine production equipment, production facilities and environmental validation
  • Must have experience with field execution of functionality testing, alarms and safety testing and integrated system testing
  • Experience in industrial automation and system controls is a plus
  • Individual may be required to execute test or generate test scripts and report or a combination of all activities

To Apply:
  • Click the "I'm interested" button below, or
  • E-mail your resume in MSWord or pdf format to careers@brevitascorp.com with the following details in the e-mail's Subject Line: US - CQV Consultant: FIRST NAME, LAST NAME.

We thank all applicants in advance; however, we will only contact the candidates whose qualifications match closely to the job requirements.
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