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

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) #J-18808-Ljbffr 3key Consulting, Inc.