Associate Engineer – Thermal Packaging Systems Cold Chain Logistics GMP Documentation & Project Support (JP15311)
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Job Location:
Thousand Oaks, CA - USA
Hourly Salary:
$ 28 - 34
Posted on:
8 hours ago
Vacancies:
1 Vacancy
Job Summary
Job Title: Associate Engineer Thermal Packaging Systems / Cold Chain Logistics / GMP Documentation & Project Support - (JP15311)
Location: Thousand Oaks CA. 91320 (Hybrid)
Employment Type: Contract
Business Unit: Commercial Drug Product
Duration: 6 months (with likely extensions and/or conversion to permanent)
Posting Date: 04/29/26
Pay Rate: $28 - $34/hour W2
Notes: Only qualified candidates need apply. Hybrid Set Up - 2 days onsite per week. Working Hours: Standard 8AM - 5PM
3Key Consulting is hiring an Associate Engineer Thermal Packaging Systems / Cold Chain Logistics / GMP Documentation & Project Support 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 clients Thousand Oaks CA. facility. This role is responsible for supporting TES project management and documentation activities. Under the guidance of senior staff the individual will apply engineering principles and adhere to current SOPs to support the design qualification and implementation of thermal packaging addition the role includes assisting with transportation laboratory testing conducting experimental studies and documenting results in compliance with SOPs.
Why is the Position Open
Supplement additional workload on team.
Top Must Have Skills:
Day to Day Responsibilities:
Basic Qualifications:
Red Flags:
Interview process:
Phone interview followed by in person interview onsite
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.
Location: Thousand Oaks CA. 91320 (Hybrid)
Employment Type: Contract
Business Unit: Commercial Drug Product
Duration: 6 months (with likely extensions and/or conversion to permanent)
Posting Date: 04/29/26
Pay Rate: $28 - $34/hour W2
Notes: Only qualified candidates need apply. Hybrid Set Up - 2 days onsite per week. Working Hours: Standard 8AM - 5PM
3Key Consulting is hiring an Associate Engineer Thermal Packaging Systems / Cold Chain Logistics / GMP Documentation & Project Support 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 clients Thousand Oaks CA. facility. This role is responsible for supporting TES project management and documentation activities. Under the guidance of senior staff the individual will apply engineering principles and adhere to current SOPs to support the design qualification and implementation of thermal packaging addition the role includes assisting with transportation laboratory testing conducting experimental studies and documenting results in compliance with SOPs.
Why is the Position Open
Supplement additional workload on team.
Top Must Have Skills:
- Knowledge of GMP-Bio/Pharma background
- Project management and documentation
- Proven written and oral communication skills
Day to Day Responsibilities:
- Track TES project progress and update project dashboard
- Author and revise controlled documents in document management system
- Assist lab test execution and conduct characterization studies for TES projects
- Participate in shipping solution qualification projects
- Lead weekly team meetings to review project updates and facilitate team discussions
- Maintain and update the SharePoint project management dashboard to track progress
- Support shipping solution qualification projects and troubleshooting activities
- Assist with laboratory test execution perform thermal experiments analyze data and generate reports
- Author and revise controlled documents (SOPs PCS RPTs APPXs) within CDOCS and PLM systems
- Collaborate with cross-functional teams on protocol reviews test preparation change control processes and deviation/CAPA management
- Utilize MS Office Suite (Excel Word Visio PowerPoint etc.) to develop documentation
Basic Qualifications:
- Bachelor degree OR Associate degree and 4 years of experience OR High school diploma / GED and 6 years of experience
- Bachelors degree in engineering or a related science field (biotechnology chemical or mechanical engineering preferred)
- Prior laboratory experience and knowledge of pharmaceutical GMP/GDP practices
- Experience with project management and GDocP (Good Documentation Practices) preferred
- Strong verbal and written communication skills
- Demonstrated ability to execute engineering tasks in accordance with SOPs and established procedures
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 interview followed by in person interview onsite
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
Required Experience:
IC
