Engineer, Container Closure Integrity Equipment Qualification​/Validation​/Testing; JP

Engineer, Container Closure Integrity Equipment Qualification/Validation/Testing (JP15882)

• Thousand Oaks, CA
• Biotech/Pharmaceutical

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

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.

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

Supplement additional workload on the team

• Documentation writing (procedures, technical assessments, engineering drawings, etc)
• Solid modeling (fixture development)
• Meetings
• Testing

• Documentation writing (procedures, technical assessments, engineering drawings, etc)
• Solid modeling (fixture development)
• Meetings
• Testing

Masters Degree OR Bachelor’s 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.

• Less than a bachelors degree
• A non-STEM bachelors degree
• No work experience (internship okay)

• Initial phone call
• Panel interview (2-3 people on call)