Engineer, Container Closure Integrity Testing, Drug Delivery Device (JP15882)

3key Consulting, Inc.; Thousand Oaks (CA); On-site; USD 58,000 - 65,000; Part time

Job summary

3 Key Consulting, Inc. is hiring an Engineer for a 18-month contract in Thousand Oaks, CA, to support container closure integrity testing for a leading biopharma client. The role combines lab and office work with heavy documentation requirements and expected onsite presence.

Requirements include a Master’s or Bachelor’s with relevant experience in medical/biopharma development or operations, and strong skills in documentation, solid modeling, meetings, and testing.

Qualifications

• Masters degree or Bachelor’s degree with 2 years in medical/biopharma development or operations.
• Associate degree with 6 years in medical/biopharma development or operations.

Responsibilities

• Support development of technical documentation for CCIT testing.
• Execute protocols to support development.
• Write technical documentation to support findings and results.
• Documentation-heavy role with emphasis on records.
• Split between lab and office work.

Skills

Documentation writing

Solid modeling

Meetings

Testing

Education

Masters degree

Bachelor’s degree with 2 years experience

Job description

Engineer, Container Closure Integrity Testing, Drug Delivery Device (JP15882)

• Thousand Oaks, CA
• Biotech/Pharmaceutical

Job Title:Engineer, Container Closure Integrity Testing, Drug Delivery Device (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:10/7/2026

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 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.

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)