Engineer Prefilled Syringe Design and Test JP13742

Job Title: Engineer Prefilled Syringe Design and Test (JP13742
Location: Thousand Oaks CA. 91320
Business Unit: Prefilled Syringes & Lyo Kit Platforms
Employment Type: Contract
Duration: 1 year with likely extensions and/or conversion to a permanent position.
Rate: $36 $41/hour W2
Posting Date: 02/26/2025.
Notes: Only qualified candidates need apply.


3 Key Consulting is hiring! We are recruiting an Engineer Prefilled Syringe Design and Test for a consulting engagement with our direct client a leading global biotechnology company.

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 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.

Top Must Have Skill Sets:
Hands on Laboratory Experience in a GLP Setting (Science or Engineering Lab)
GMP and GDP Technical Writing Skills
CAD experience or knowledge (such as Solidworks)

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 productbased 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 and GDP 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. FillFinish 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.

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 fillfinish 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 crossfunctional 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

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

Preferred Qualifications:
Bachelors 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 (fillfinish)
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 text 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 the following standards and regulations: Quality System Regulation 21CFR820; Quality Management System for medical device/component manufacturers ISO 13485 Risk Management for Medical Devices ISO 14971; EU Medical Device Regulation 2017/745

Red Flags:
No GxP laboratory experience
2. No GDP experience
3. Only academic technical writing experience (nonindustry setting)

Why is the Position Open
Backfill

Interview Process:
Virtual 1 on 1 interview with hiring manager
Virtual 1 on 1 interview with organization department manager
Panel interview 23 colleagues)

We invite qualified candidates to send your resume to If you decide that youre not interested in pursuing this particular position please feel free to take a look at the other positions on our website www.3keyconsulting/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.