3key Consulting, Inc.
Engineer – Combination Device Design, Development & LCM (JP14435)
3key Consulting, Inc., Thousand Oaks, California, United States, 91362
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 design controls; including (but not limited to) design verification and transfer Understanding of risk assessments including hazard and probability analysis Experience with investigations and quality records Laboratory and electronic lab notebook experience Statistical Analysis software (Minitab or JMP) Experience with Instron force testers using BlueHill Universal Test method development, GR&R, and test fixture design Ability to work independently and dynamically across functional teams Strong technical writing and verbal communication skills including technical presentations (i.e., PowerPoint) Ability to support complex workstreams under demanding timeline Understanding of Quality System Regulation – 21CFR820; ISO 13485; ISO 14971; EU Medical Device Regulation – 2017/745
Employee Value Proposition
Unique industry opportunity Experience
Interview Process
Interview will consist of a virtual interview with the hiring manager (1-1) and a separate panel interview (3-1). Interviews will be scheduled following resume review period.
How to Apply
Please send your resume to resumes@3keyconsulting.com. For other opportunities, visit our careers page at www.3keyconsulting.com/careers. You may also share this opportunity with colleagues who might be interested.
#J-18808-Ljbffr
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 design controls; including (but not limited to) design verification and transfer Understanding of risk assessments including hazard and probability analysis Experience with investigations and quality records Laboratory and electronic lab notebook experience Statistical Analysis software (Minitab or JMP) Experience with Instron force testers using BlueHill Universal Test method development, GR&R, and test fixture design Ability to work independently and dynamically across functional teams Strong technical writing and verbal communication skills including technical presentations (i.e., PowerPoint) Ability to support complex workstreams under demanding timeline Understanding of Quality System Regulation – 21CFR820; ISO 13485; ISO 14971; EU Medical Device Regulation – 2017/745
Employee Value Proposition
Unique industry opportunity Experience
Interview Process
Interview will consist of a virtual interview with the hiring manager (1-1) and a separate panel interview (3-1). Interviews will be scheduled following resume review period.
How to Apply
Please send your resume to resumes@3keyconsulting.com. For other opportunities, visit our careers page at www.3keyconsulting.com/careers. You may also share this opportunity with colleagues who might be interested.
#J-18808-Ljbffr