Job Title: Engineer Mechanical Design & Test Method Development (JP14414)
Location: Thousand Oaks CA. 91320Employment Type: ContractBusiness Unit: Mechanical Design EngineeringDuration: 18 months (with likely extensions and/or conversion to permanent)Posting Date: 09/04/25Pay Rate: $36 - $41/hour W2Notes: Only qualified candidates need apply. Thousand Oaks Local Candidates Only. Potential for Hybrid. 18 months with possible 18-month extension based on performance3 Key Consulting is hiring an Engineer for a consulting engagement with our direct client a leading global biopharmaceutical company.Job Description:The ideal candidate is a junior to mid-level Mechanical or Biomedical Engineer (Bachelors degree 13 years of experience Masters acceptable) with hands-on pharmaceutical or biomedical industry experience. They must demonstrate proficiency in statistical analysis Gauge R&R and optical measurement devices while having basic working knowledge of CAD/SolidWorks for simple designs. Strong familiarity with GMP documentation practices and ability to write technical documents is critical. The best fit will be local to Thousand Oaks or open to relocation motivated to work in a hybrid on-site model and able to show problem-solving ability and a willingness to learn.Position involves support of senior staff in the initiation design and delivery of projects particularly for the Combination Product Operations MS&T - Physical Sciences and Engineering (PSE) organization. (See day-to-day responsibilities below).The ideal candidate enjoys tackling challenges and excels at organizing information from numerous sources to provide well-constructed deliverables. This individual has a passion for modeling analytics and technology. The successful candidate will be given opportunities to apply their expertise to enhance the way data is used to inform and make decisions. This may include but is not limited to the following:- Collaborate with Engineers using the system to edit develop and run automated experimental protocols.
- Knowledge on Equipment and Method validation principles generation of Lifecycle Documentation such as FAT/SAT IQ/OQ equipment characterization protocols Gauge Repeatability and Reproducibility studies
- Assisting Engineers to successfully develop transfer and execute processes on the integrated platforms and equipment.
- Developing enhancing automating and managing test data
- Network with manufacturing and quality organizations internal to client
- Ensuring all tasks and responsibilities are performed according to industry-leading scientific standards & accurately documented per SOPs
- Monitoring technological developments in the field & evaluation of new technologies
Why is the Position OpenSupplement additional workload on teamTop Must Have Skills:- Statistical analysis and knowledge of Gage R&R (Repeatability & Reproducibility)
- Knowledge of Optical measurement devices force testers BLE testing
- Test method development CAD design Solid works mechanical modeling
Day to Day Responsibilities:- Support FTE Engineers developing Methods and performing testing
- Employs basic engineering skills and practices to gather user requirements and translate them into technical documentation.
- Assist with project definition by performing engineering studies and assessment for automated test systems installations.
- Perform field evaluations of existing systems and provide engineering design recommendations.
- Create and revise documentations
- Development and lifecycle management of Physical GMP Test Methods lifecycle management of integrated testing machines development and validation of test methods.
Basic Qualifications:Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experiencePreferred Qualifications:Preferred Skills- Experience working in a regulated industry exposure to GMPs
- Excellent verbal and written communication skills to communicate project status and risks associated with integrated timelines to leadership
- Statistical analysis and knowledge of Gage R&R
- Knowledge of Optical measurement devices force testers BLE testing
- Test method development CAD design Solid works mechanical modeling
- Manufacturing experience IQ OQ and PQ
Preferred Traits:- Passion for proactively identifying opportunities through creative data analysis and modeling
- Intellectual curiosity with ability to learn new concepts/frameworks algorithms and technology rapidly as needs arise
- Ability to manage multiple competing priorities simultaneously experience with MS Project Smartsheet
Red Flags:- Zero experience with combination products but willing to consider training a junior engineer.
- No experience with combination products (e.g. injectors)
- No GMP documentation experience
- Candidates commuting from too far away (preference: local to Thousand Oaks or willing to relocate)
- Overqualified candidates (6 years pharmaceutical experience likely to leave quickly; PhDs too senior)
Interview process:
Phone screening with hiring manager followed by final panel interview.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. Regards
3KC Talent Acquisition Team
Job Title: Engineer Mechanical Design & Test Method Development (JP14414)Location: Thousand Oaks CA. 91320Employment Type: ContractBusiness Unit: Mechanical Design EngineeringDuration: 18 months (with likely extensions and/or conversion to permanent)Posting Date: 09/04/25Pay Rate: $36 - $41/hour W2...
Job Title: Engineer Mechanical Design & Test Method Development (JP14414)
Location: Thousand Oaks CA. 91320Employment Type: ContractBusiness Unit: Mechanical Design EngineeringDuration: 18 months (with likely extensions and/or conversion to permanent)Posting Date: 09/04/25Pay Rate: $36 - $41/hour W2Notes: Only qualified candidates need apply. Thousand Oaks Local Candidates Only. Potential for Hybrid. 18 months with possible 18-month extension based on performance3 Key Consulting is hiring an Engineer for a consulting engagement with our direct client a leading global biopharmaceutical company.Job Description:The ideal candidate is a junior to mid-level Mechanical or Biomedical Engineer (Bachelors degree 13 years of experience Masters acceptable) with hands-on pharmaceutical or biomedical industry experience. They must demonstrate proficiency in statistical analysis Gauge R&R and optical measurement devices while having basic working knowledge of CAD/SolidWorks for simple designs. Strong familiarity with GMP documentation practices and ability to write technical documents is critical. The best fit will be local to Thousand Oaks or open to relocation motivated to work in a hybrid on-site model and able to show problem-solving ability and a willingness to learn.Position involves support of senior staff in the initiation design and delivery of projects particularly for the Combination Product Operations MS&T - Physical Sciences and Engineering (PSE) organization. (See day-to-day responsibilities below).The ideal candidate enjoys tackling challenges and excels at organizing information from numerous sources to provide well-constructed deliverables. This individual has a passion for modeling analytics and technology. The successful candidate will be given opportunities to apply their expertise to enhance the way data is used to inform and make decisions. This may include but is not limited to the following:- Collaborate with Engineers using the system to edit develop and run automated experimental protocols.
- Knowledge on Equipment and Method validation principles generation of Lifecycle Documentation such as FAT/SAT IQ/OQ equipment characterization protocols Gauge Repeatability and Reproducibility studies
- Assisting Engineers to successfully develop transfer and execute processes on the integrated platforms and equipment.
- Developing enhancing automating and managing test data
- Network with manufacturing and quality organizations internal to client
- Ensuring all tasks and responsibilities are performed according to industry-leading scientific standards & accurately documented per SOPs
- Monitoring technological developments in the field & evaluation of new technologies
Why is the Position OpenSupplement additional workload on teamTop Must Have Skills:- Statistical analysis and knowledge of Gage R&R (Repeatability & Reproducibility)
- Knowledge of Optical measurement devices force testers BLE testing
- Test method development CAD design Solid works mechanical modeling
Day to Day Responsibilities:- Support FTE Engineers developing Methods and performing testing
- Employs basic engineering skills and practices to gather user requirements and translate them into technical documentation.
- Assist with project definition by performing engineering studies and assessment for automated test systems installations.
- Perform field evaluations of existing systems and provide engineering design recommendations.
- Create and revise documentations
- Development and lifecycle management of Physical GMP Test Methods lifecycle management of integrated testing machines development and validation of test methods.
Basic Qualifications:Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experiencePreferred Qualifications:Preferred Skills- Experience working in a regulated industry exposure to GMPs
- Excellent verbal and written communication skills to communicate project status and risks associated with integrated timelines to leadership
- Statistical analysis and knowledge of Gage R&R
- Knowledge of Optical measurement devices force testers BLE testing
- Test method development CAD design Solid works mechanical modeling
- Manufacturing experience IQ OQ and PQ
Preferred Traits:- Passion for proactively identifying opportunities through creative data analysis and modeling
- Intellectual curiosity with ability to learn new concepts/frameworks algorithms and technology rapidly as needs arise
- Ability to manage multiple competing priorities simultaneously experience with MS Project Smartsheet
Red Flags:- Zero experience with combination products but willing to consider training a junior engineer.
- No experience with combination products (e.g. injectors)
- No GMP documentation experience
- Candidates commuting from too far away (preference: local to Thousand Oaks or willing to relocate)
- Overqualified candidates (6 years pharmaceutical experience likely to leave quickly; PhDs too senior)
Interview process:
Phone screening with hiring manager followed by final panel interview.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. Regards
3KC Talent Acquisition Team
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