Job Title: Associate Engineer – Thermal Engineering Lab Testing & Equipment Qualification (GMP) - (JP15950)
Location: Thousand Oaks, CA. 91320 (hybrid)
Employment Type: Contract
Business Unit: Manufacturing Science & Technology
Duration: 6+ months (with likely extensions and/or conversion to permanent)
Posting Date: 10/8/26
Pay Rate: $30 - $34/hour W2
Notes: Only qualified candidates need apply.
3 Key Consulting is hiring an Associate Engineer -
Thermal Engineering Lab Testing & Equipment Qualification (GMP) for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:The Associate Engineer position is part of the Thermal Engineering Systems (TES) group at our client’s Thousand Oaks, CA. facility. The individual will apply engineering principles and follow current SOPs to execute lab related testing per approved protocols. Under supervision by senior personnel, the individual will set up a variety of equipment and instruments, conduct experimental studies, and document the results following SOPs.
Why is the Position Open?Supplement additional workload on team
Top Must Have Skills:- Knowledge of cGMP-Bio/Pharma background
- Lab testing experience/knowledge and lab management
- Proven written and oral communication skills
Day to Day Responsibilities:- Execute all lab related testing per test protocols in accordance with operating standards, SOPs and regulatory requirements, while understanding safety precautions
- Operate & maintain all lab equipment, e.g., Vibration Systems, Environmental Chambers, and Vacuum Systems
- and manage budget/expense & inventory at levels to satisfy testing demand
- Plan and schedule all lab related activities
- Author and revise controlled documents in document management system
- Conduct characterization studies for TES projects
- Responsible for planning and scheduling all lab related activities, such equipment calibration, maintenance, lab tour, etc.
- Manage lab budget/expense and supply inventory
- Collaborate with cross-functional teams (i.e. Research and Development, QA/QC, Supply Chain, Maintenance, Manufacturing, Regulatory) on protocol review, testing preparation, change control process, deviation & CAPA, and controlled documentation
- Assist Engineers with internal experiments and studies; provide guidance on test method to be used
Basic Qualifications:- Bachelor degree OR Associate degree and 4 years of experience OR High school diploma / GED and 6 years of experience
- Able to troubleshoot and perform general maintenance on equipment to keep a test running
- Proficient in MS Office Suite (Excel, Word, Visio, PPT, etc)
- Engineering or Science degree: biotechnology, chemical or mechanical preferred;
- Prior lab/manufacturing/production experience/knowledge in GMP/GLP environment;
- Evidence of completing engineering tasks according to SOPs or instructions;
- Knowledge of industry testing standards, i.e. ASTM and ISTA, is a plus;
- Experience in the Bio-Tech or Pharmaceutical Industry preferred;
- Good oral/written communication skills;
- Ability to prioritize tasks and maintain functionality in the lab
- Able to lift up to 60 lbs repeatedly without assistance
Red Flags:- Candidates who lack relevant skills
- Candidates who do not meet the qualification requirements
- Candidates who were separated from previous employment due to unethical behaviors
Interview process:
Phone screening followed by in person
We invite qualified candidates to send your resume to
resumes@3keyconsulting.com
. If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.