Engineer, Medical Devices (JP12013)
Company: 3 Key Consulting
Location: Thousand Oaks
Posted on: April 1, 2026
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Job Description:
Job Title: Engineer, Medical Devices (JP12013) Location:
Thousand Oaks, CA. 91320 Business Unit: PFS And Lyo Kit Platforms
Employment Type: Contract Duration: 1 years with possible
extensions or conversion to FTE Rate : $37 - $41/hour W2 Posting
Date: 11/27/2023 Notes: ONSITE - no remote, heavy lab role.
considering candidates in a reasonable radius from the thousand
oaks site. 3 Key Consulting is recruiting an Engineer for a
consulting engagement with our direct client, a leading global
biotechnology company. Ideal Candidate : Excellent communication,
forced testing software experience, design verification testing,
proficiency with MS suite. Bachelors relevant engineering or any
scientific field as long as they have hands on Laboratory
Experience in a GLP Setting (Science or Engineering Lab). Willing
to consider those with relevant internship experience. Job
Description: The Device Engineer will participate in the design,
development, and lifecycle management design control activities for
commercialized drug delivery devices. This role includes technical
operations support for combination product development to global
launch, clinical and commercial manufacturing, failure
investigation, design change evaluation, development and execution
of test procedures, and continuous improvement initiatives. Scope
includes mechanical delivery devices, such as Prefilled syringes.
The qualified candidate will be part of a sustaining device
engineering team that ensures design history files of these
mechanical delivery devices are maintained. The engineer will
participate in cross functional teams, leading device design
activities such as the development of product enhancements,
analytical failure analysis and implementation of design solutions,
assessment of proposed changes, support product launches, and
defend inspection and ensure the follow through of commitments.
Basic Qualifications: Master degree OR Bachelor degree and 2 years
of experience OR Associate degree and 6 years of experience Top
Must Have Skill Sets: Hands on Laboratory Experience in a GLP
Setting (Science or Engineering Lab) Good Communication and
Technical Writing Skills Ability to Multitask Day to Day
Responsibilities: The device engineer will support a senior
engineer on a variety of projects related to laboratory testing,
life cycle management, and product-based initiatives regarding
prefilled syringes in both the commercial and developmental space.
The engineer will be expected to author protocols, reports, and
further technical documentation while adhering to GMP standards.
Laboratory testing will primarily include the use of an Instron
force tester and vision systems. The identified candidate must be
able to lift up to 50 lbs for receipt and transferring of material.
Fill-Finish experience is a bonus but not mandatory. Engineer will
be evaluated on ability to complete a wide variety of supporting
tasks for projects in a timely manner while maintaining a high
standard of quality. Employee Value Proposition: great opportunity
for growth in career Why is the Position Open? Supplement
additional workload on team. Red Flags: No previous industry or
laboratory experience Unfamiliar with Good Documentation Practices
Poor communication No technical writing. Interview Process:
Individual Interviews (x2) - Webex or In-person Panel Interview
(x1) – Webex We invite qualified candidates to send your resume to
recruiting@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. Regards, 3KC Talent Acquisition Team
Keywords: 3 Key Consulting, Lancaster , Engineer, Medical Devices (JP12013), Engineering , Thousand Oaks, California
