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CQV Validation Engineer, Biotech GMP Equipment – Remote (JP15497)
Job Location:
Job Location:
Thousand Oaks, CA - USA
Hourly Salary:
$ 46 - 52
Hourly Salary:
Posted:
18 June 2026 (30+ days ago)
Posted:
Application Deadline:
14 October 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Job Title:CQV Validation Engineer Biotech GMP Equipment Remote (JP15497)
Location:Thousand Oaks CA. 91320
Employment Type:Contract
Business Unit:Engineering Systems
Duration:12 months with likely extensions and/or conversion to permanent
Posting Date:06/16/2026
Pay Rate:$46 - $52/hour W2 with benefits
Notes:Fully Remote.
3 Key Consulting is hiring aC&Q Validation Engineer for a consulting engagement with our direct client a leading global biopharmaceutical company.
Job Description:
Primarily responsible for planning coordinating executing and documenting periodic reviews of GMP equipment to ensure continued state of validation compliance with regulatory requirements and suitability for intended use. The role partners with Engineering Manufacturing Quality Assurance Validation and Maintenance teams to assess equipment performance maintenance history calibration status deviations change controls and overall lifecycle management.
Key skills and requirements:
Demonstrable experience in a pharmaceutical biotech or life science organization in a C&Q/CQV/validation maintenance role.
Knowledge of cGMP commissioning/qualification/validation practices.
Familiarity with biotech/pharmaceutical manufacturing equipment.
Familiarity with Kneat Gx Platform or other digital C&Q systems.
Experience working with cross-functional stakeholders.
Knowledge of quality assurance principles including deviations and change control systems.
Effective communication skills both verbal and written.
Able to think analytically with the ability to resolve issues.
Able to manage own time efficiently.
Position could be extended to up to 3 years
Why is the Position Open
Planned Project.
Top Must Have Skills:
Experience in commissioning/qualification/validation experience in a GMP environment knowledge ofbiotech/pharmaceutical manufacturing equipment
Day to Day Responsibilities:
Execute periodic reviews of GMP equipment according to approved procedures and schedules. Assess
equipment records including work orders deviations and change control records.
Evaluate equipment records to verify continued fitness for intended use.
Generate and/or revise periodic review reports.
Collaborate with Manufacturing System Owners Validation and Quality teams as needed.
Schedule and lead review meetings as needed to resolve issues.
Ensure reviews are completed within established timelines and regulatory expectations.
Maintain periodic review trackers and metrics.
Identify opportunities to improve the equipment periodic review process.
Other duties may be assigned to this role.
Basic Qualifications:
Master degree or Bachelor degree and 2 years of experience or Associate degree and 6 years of experience or high school diploma / GED and 8 years of experience
Employee Value Proposition:
Industry experience.
Red Flags:
Short tenures at previous jobs (<2 years)
No experience in commissioning/qualification/validation
Interview process:
1-2 Stages of interview Video interview (Teams)
We invite qualified candidates to sendyour resume to. Ifyou decide that youre not interested in pursuing this particular position please feel free to take a look at the other positions on our You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.
Location:Thousand Oaks CA. 91320
Employment Type:Contract
Business Unit:Engineering Systems
Duration:12 months with likely extensions and/or conversion to permanent
Posting Date:06/16/2026
Pay Rate:$46 - $52/hour W2 with benefits
Notes:Fully Remote.
3 Key Consulting is hiring aC&Q Validation Engineer for a consulting engagement with our direct client a leading global biopharmaceutical company.
Job Description:
Primarily responsible for planning coordinating executing and documenting periodic reviews of GMP equipment to ensure continued state of validation compliance with regulatory requirements and suitability for intended use. The role partners with Engineering Manufacturing Quality Assurance Validation and Maintenance teams to assess equipment performance maintenance history calibration status deviations change controls and overall lifecycle management.
Key skills and requirements:
Demonstrable experience in a pharmaceutical biotech or life science organization in a C&Q/CQV/validation maintenance role.
Knowledge of cGMP commissioning/qualification/validation practices.
Familiarity with biotech/pharmaceutical manufacturing equipment.
Familiarity with Kneat Gx Platform or other digital C&Q systems.
Experience working with cross-functional stakeholders.
Knowledge of quality assurance principles including deviations and change control systems.
Effective communication skills both verbal and written.
Able to think analytically with the ability to resolve issues.
Able to manage own time efficiently.
Position could be extended to up to 3 years
Why is the Position Open
Planned Project.
Top Must Have Skills:
Experience in commissioning/qualification/validation experience in a GMP environment knowledge ofbiotech/pharmaceutical manufacturing equipment
Day to Day Responsibilities:
Execute periodic reviews of GMP equipment according to approved procedures and schedules. Assess
equipment records including work orders deviations and change control records.
Evaluate equipment records to verify continued fitness for intended use.
Generate and/or revise periodic review reports.
Collaborate with Manufacturing System Owners Validation and Quality teams as needed.
Schedule and lead review meetings as needed to resolve issues.
Ensure reviews are completed within established timelines and regulatory expectations.
Maintain periodic review trackers and metrics.
Identify opportunities to improve the equipment periodic review process.
Other duties may be assigned to this role.
Basic Qualifications:
Master degree or Bachelor degree and 2 years of experience or Associate degree and 6 years of experience or high school diploma / GED and 8 years of experience
Employee Value Proposition:
Industry experience.
Red Flags:
Short tenures at previous jobs (<2 years)
No experience in commissioning/qualification/validation
Interview process:
1-2 Stages of interview Video interview (Teams)
We invite qualified candidates to sendyour resume to. Ifyou decide that youre not interested in pursuing this particular position please feel free to take a look at the other positions on our You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.
Required Experience:
IC
