ZipRecruiter

Log In

1

Commissioning Qualification Validation Cqv Jobs (NOW HIRING)

Wood Plc

It provides process engineering, process design, and commissioning - qualification - validation (CQV) services to pharmaceutical/biotechnology clients worldwide. For projects of every scale, we ...

Biovire

Manager, Validation

Brighton, MI · On-site

The Role The Manager, Validation leads commissioning, qualification, validation (CQV), and computer system validation (CSV) activities across the Brighton site. This role provides technical oversight ...

Biovire

Manager, Validation

Brighton, MI · On-site

$100K - $120K/yr

The RoleThe Manager, Validation leads commissioning, qualification, validation (CQV), and computer system validation (CSV) activities across the Brighton site. This role provides technical oversight ...

Biovire

Head of Validation

Brighton, MI · On-site

The Role The Manager, Validation leads commissioning, qualification, validation (CQV), and computer system validation (CSV) activities across the Brighton site. This role provides technical oversight ...

Validation & Engineering Group, Inc

PR · On-site

CQV Specialist Utilities Description ... Supports commissioning, qualification, validation, and maintenance programs in GMP-regulated ...

Genesis AEC

Validation Engineer I

Irvine, CA · Hybrid

$60K - $70K/yr

WHAT YOU WILL DO As a Validation Engineer I, you will be part of our Commissioning, Qualification, and Validation (CQV) team that ensures that projects are installed and operated to meet design and ...

Genesis AEC

Validation Engineer I

Irvine, CA · On-site

$60K - $70K/yr

WHAT YOU WILL DO As a Validation Engineer I, you will be part of our Commissioning, Qualification, and Validation (CQV) team that ensures that projects are installed and operated to meet design and ...

previous page

Showing results 41-60

All JobsCommissioning Qualification Validation Cqv Jobs

Commissioning Qualification Validation Cqv information

See salary details

$22

$51

$78

How much do commissioning qualification validation cqv jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for commissioning qualification validation cqv in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a commissioning qualification validation (CQV) professional, and why are they important?

To excel as a CQV professional, you need a solid background in engineering or life sciences, comprehensive knowledge of Good Manufacturing Practice (GMP), and experience with commissioning and validation processes. Familiarity with industry-standard software like ValGenesis, TrackWise, and documentation management systems, as well as certifications such as ISPE CQV or Six Sigma, is often required. Attention to detail, strong problem-solving abilities, and effective communication are crucial soft skills in this field. These competencies ensure equipment and processes meet regulatory standards, guarantee product quality, and support successful project delivery in highly regulated industries.

What are some typical challenges faced by commissioning qualification validation (CQV) professionals during facility start-up projects?

CQV professionals often encounter challenges such as tight project timelines, evolving regulatory requirements, and coordination among cross-functional teams. During facility start-up, balancing documentation accuracy with rapid progress can be demanding, especially when unexpected technical issues arise. Additionally, aligning the expectations of engineering, quality assurance, and operations departments requires strong communication and adaptability. By proactively addressing these challenges, CQV professionals help ensure a smooth transition from construction to validated production.

What is a commissioning qualification validation (CQV) professional?

Commissioning, Qualification, and Validation (CQV) professionals are specialists who ensure that equipment, systems, and processes in industries like pharmaceuticals, biotechnology, and manufacturing meet regulatory standards and function as intended. They are responsible for planning, executing, and documenting activities that demonstrate compliance with quality and safety regulations. CQV experts play a critical role in bringing new facilities and systems into operation, guaranteeing that everything is tested and verified according to industry guidelines. Their work helps prevent failures, enhance product quality, and ensure patient or consumer safety.

What is the difference between Commissioning Qualification Validation Cqv vs Equipment Validation Specialist?

AspectCommissioning Qualification Validation CqvEquipment Validation Specialist
CredentialsGMP, FDA, or industry-specific certificationsGMP, FDA, or industry-specific certifications
Work EnvironmentPharmaceutical, biotech, or manufacturing facilities during project startupManufacturing or laboratory environments focusing on equipment performance
Employer & Industry UsageUsed in regulated industries for system and process validationUsed for validating individual equipment and systems

While both roles involve validation processes, Cqv focuses on the overall commissioning, qualification, and validation of systems and processes during facility startup. Equipment Validation Specialists primarily validate specific equipment performance. Both require similar certifications and work in regulated manufacturing environments, but their scope differs in focus and responsibilities.

More about Commissioning Qualification Validation Cqv jobs
What cities are hiring for Commissioning Qualification Validation Cqv jobs? Cities with the most Commissioning Qualification Validation Cqv job openings:
What states have the most Commissioning Qualification Validation Cqv jobs? States with the most job openings for Commissioning Qualification Validation Cqv jobs include:
What job categories do people searching Commissioning Qualification Validation Cqv jobs look for? The top searched job categories for Commissioning Qualification Validation Cqv jobs are:
Commissioning Qualification Validation Cqv jobs near you
Infographic showing various Commissioning Qualification Validation Cqv job openings in the United States as of August 2026, with employment types broken down into 91% Full Time, 7% Part Time, and 2% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Senior CQV Engineer - GMP Equipment, Utilities & Facilities Qualification - (JP15486)

3 Key Consulting

Thousand Oaks, CA • Hybrid

$66 - $72/hr

Full-time

Re-posted 23 days ago

Job description

Job Title: Senior CQV Engineer – GMP Equipment, Utilities & Facilities Qualification - (JP15486)
Location: Thousand Oaks, CA. 91320 (Hybrid)
Employment Type: Contract
Business Unit: Engineering Systems
Duration: 1+ year (with likely extensions and/or conversion to permanent)
Posting Date: 06/16/26
Pay Rate: $66 - $72/hour W2
Notes: Only qualified candidates need apply. Local, onsite at least 3 days weekly 8-5
3 Key Consulting is hiring a Senior CQV Engineer – GMP Equipment, Utilities & Facilities Qualification  for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Primarily responsible for leading and/or executing commissioning and qualification activities on new or modified GMP analytical and process equipment, utilities, and facilities. Responsibilities include generating/reviewing/executing C&Q protocols, plans, and summary reports. Works with project teams and SMEs to develop testing strategies. Participates in project meetings to inform stakeholders on progress of C&Q activities.
Why is the Position Open?
Planned Project.
Top Must Have Skills:
  • Experience in commissioning/qualification/validation
  • Experience in a GMP environment

Day to Day Responsibilities:
  • Plan and track implementation of commissioning & qualification actions/documentation versus project(s) timelines.
  • Work with project teams to develop the commissioning and qualification strategy and document in qualification plans.
  • Generate/evaluate qualification/validation protocols including IQ, OQ, FT, PQ protocols and final reports for new or modified GMP analytical and process equipment, utilities, and facilities.
  • Execute IQ, OQ, FT, PQ protocols, which may involve protocol discrepancies, investigation, and corrective action activities for new or modified GMP analytical and process equipment, utilities, and facilities.
  • Ensure that Qualification/Validation plans are generated and updated for all ongoing projects.
  • Prepare, evaluate and approve technical and GMP linked documentation such as URS, FMEA, impact/risk assessment, master plans, qualification/validation documentation.
  • Develop and/or execute FAT/SAT and other commissioning activities for new GMP systems in collaboration with both internal and external partners.
  • May include conducting validation maintenance activities including performing and scheduling periodic reviews.
  • Other duties may be assigned to this role.

Basic Qualifications:
Doctorate degree OR Masters degree and 2 years of experience OR Bachelors degree and 4 years of experience OR Associates degree and 8 years of experience OR High school diploma / GED and 10 years of experience
 
  • Demonstrable experience in a pharmaceutical, biotech, or life science organization in a C&Q/CQV role.
  • Knowledge of cGMP commissioning/qualification/validation practices.
  • Familiarity with Kneat Gx Platform or other digital C&Q systems.
  • Experience working with cross-functional stakeholders.
  • Knowledge of quality assurance principles.
  • Experience working within project teams and multiple projects in parallel.
  • Effective communication skills, both verbal and written.
  • Able to think analytically with the ability to resolve issues.
  • Able to manage own time efficiently.

Red Flags:
Short tenures at previous jobs (?2 years), not local and not willing to relocate
Interview process:
1-2 Stages of interview | Video interview (Teams)
We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.