Enter a job title or keyword
Senior CQV Engineer – GMP Equipment, Utilities & Facilities Qualification (JP15486)
Job Location:
Job Location:
Thousand Oaks, CA - USA
Hourly Salary:
$ 66 - 72
Hourly Salary:
Posted:
18 June 2026 (30+ days ago)
Posted:
Application Deadline:
12 October 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
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:
Day to Day Responsibilities:
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
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 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 (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 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:
Senior IC
