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Engineer – Combination Device Design, Development & LCM; JP

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: 3key Consulting, Inc.
Full Time position
Listed on 2026-01-12
Job specializations:
  • Engineering
    Quality Engineering, Biomedical Engineer, Manufacturing Engineer, Medical Device Industry
Salary/Wage Range or Industry Benchmark: 36 - 41 USD Hourly USD 36.00 41.00 HOUR
Job Description & How to Apply Below
Position: Engineer – Combination Device Design, Development & LCM (JP14435)

Overview

Job Title: Engineer – Combination Device Design, Development & LCM (JP14435)

Location: Thousand Oaks, CA. 91320

Employment Type: Contract

Business Unit: PFS And Lyo Kit Platforms

Duration: 1+ years (with likely extensions and/or conversion to permanent)

Posting Date: 08/27/25

Pay Rate: $36 - $41/hour W2

Job Description

The Device Engineer will participate in the design, development, and lifecycle management of 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, defend inspection and ensure the follow through of commitments.

Why

the Position Is Open

Conversion backfill.

Top Must Have Skills
  • Hands on Laboratory Experience in a GLP Setting (Science or Engineering Lab)
  • Good Communication and Technical Writing Skills
  • Statistical Analysis
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.

The engineer will be evaluated on the ability to complete a wide variety of supporting tasks for projects in a timely manner while maintaining a high standard of quality.

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 experience

  • Adheres to strict documentation practices in a GMP regulated environment
  • Engineering competency in all conventional aspects of the subject matter, functional area, and assignments
  • Plans and performs work, independently evaluating, selecting, and adapting standard methods, and creating new solutions to engineering problems.
  • Authors and reviews technical documentation including protocols, reports, and technical assessments
  • Coordinates and executes laboratory testing to support characterization, verification, design transfer, and fill-finish efforts
  • Analyze and trend generated data by applying relevant statistical techniques to enable senior staff to make informed decisions
  • Maintains device and combination product design history files for assigned products
  • Ensure test methods and test protocols are developed in a sound and robust framework with high focus on eliminating test errors
  • Provides functional subject matter expertise to actively participate in cross-functional activities including system level root cause analysis, design changes, and change control assessments
  • Provide general laboratory support including inventory management, sample shipments, and cleanup.
  • Works with Scientists and Engineers, to assess and develop appropriate design and manufacturing specifications
Preferred Qualifications
  • Bachelor’s Degree or higher in relevant engineering or scientific field (Mechanical, Biomedical, Bioengineering)
  • Understanding of Mechanical Design Engineering Concepts
  • Experience with Final Drug Product and/or Drug Product, medical device development, commercialization and knowledge of manufacturing processes (fill-finish)
  • Experience with…
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