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Engineer, Container Closure Integrity Equipment QualificationValidationTesting (JP15882)
Job Location:
Job Location:
Thousand Oaks, CA - USA
Hourly Salary:
USD 42 - 47
Hourly Salary:
Posted:
29 September 2026 (24 days ago)
Posted:
Application Deadline:
27 December 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Job Title: Engineer Container Closure Integrity Equipment Qualification/Validation/Testing (JP15882)
Location: Thousand Oaks CA. 91320
Employment Type: Contract
Business Unit: Physical Methods Development Modelling and Emerging Methods
Duration: 18 Months with likely extensions and/or conversion to permanent
Posting Date: 09/16/2026
Pay Rate: $42 - $47/hour W2 with benefits
Notes: Will be onsite at least 2x/ week. Candidate must be within commutable distance and must be able to come on site 5 days a week if needed
3 Key Consulting is hiring an Engineer for a consulting engagement with our direct client a leading global biopharmaceutical company.
Job Description:
Position involves support of senior staff in the initiation design and delivery of projects particularly for container closure integrity testing (CCIT) related scope. Employ basic engineering skills and practices to gather user requirements and translate them into technical documentation for execution. Assist with project definition by performing engineering studies and assessment for CCIT system installations. Perform field evaluations of existing systems and provide engineering design recommendations and support development of CCIT technologies.
Bippharm or Biotech experience and/or Equipment Validation experience within another industry. Position is split between lab and office.
Equipment qualification- Equipment validation is a highly desired skillset. Will be working with other associates on testing and conducting testing themselves.
Day to day responsibilities will include supporting development of technical documentation related to CCI testing execution of protocols to support development writing of technical documentation to support findings and results.
Heavy on documentation role
Why is the Position Open
Supplement additional workload on the team
Top Must Have Skills:
Day to Day Responsibilities:
Basic Qualifications:
Masters Degree OR Bachelors degree and 2 years of related medical/biopharma development or Operations experience; OR Associate degree and 6 years of related medical/biopharma development or Operations experience.
Red Flags:
Less than a bachelors degree
A non-STEM bachelors degree
No work experience (internship okay)
Interview process:
Initial phone call
Panel interview (2-3 people on call)
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: Physical Methods Development Modelling and Emerging Methods
Duration: 18 Months with likely extensions and/or conversion to permanent
Posting Date: 09/16/2026
Pay Rate: $42 - $47/hour W2 with benefits
Notes: Will be onsite at least 2x/ week. Candidate must be within commutable distance and must be able to come on site 5 days a week if needed
3 Key Consulting is hiring an Engineer for a consulting engagement with our direct client a leading global biopharmaceutical company.
Job Description:
Position involves support of senior staff in the initiation design and delivery of projects particularly for container closure integrity testing (CCIT) related scope. Employ basic engineering skills and practices to gather user requirements and translate them into technical documentation for execution. Assist with project definition by performing engineering studies and assessment for CCIT system installations. Perform field evaluations of existing systems and provide engineering design recommendations and support development of CCIT technologies.
Bippharm or Biotech experience and/or Equipment Validation experience within another industry. Position is split between lab and office.
Equipment qualification- Equipment validation is a highly desired skillset. Will be working with other associates on testing and conducting testing themselves.
Day to day responsibilities will include supporting development of technical documentation related to CCI testing execution of protocols to support development writing of technical documentation to support findings and results.
Heavy on documentation role
Why is the Position Open
Supplement additional workload on the team
Top Must Have Skills:
- Documentation writing (procedures technical assessments engineering drawings etc)
- Solid modeling (fixture development)
- Meetings
- Testing
Day to Day Responsibilities:
- Documentation writing (procedures technical assessments engineering drawings etc)
- Solid modeling (fixture development)
- Meetings
- Testing
Basic Qualifications:
Masters Degree OR Bachelors degree and 2 years of related medical/biopharma development or Operations experience; OR Associate degree and 6 years of related medical/biopharma development or Operations experience.
Red Flags:
Less than a bachelors degree
A non-STEM bachelors degree
No work experience (internship okay)
Interview process:
Initial phone call
Panel interview (2-3 people on call)
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
