×
Register Here to Apply for Jobs or Post Jobs. X

Senior Device Engineer – Electromechanical Combination Products; Lifecycle Management, Design C

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: 3key Consulting, Inc.
Full Time position
Listed on 2026-06-18
Job specializations:
  • Engineering
    Quality Engineering, Medical Device Industry, Biomedical Engineer, Product Engineer
Salary/Wage Range or Industry Benchmark: 44 - 48.5 USD Hourly USD 44.00 48.50 HOUR
Job Description & How to Apply Below
Position: Senior Device Engineer – Electromechanical Combination Products (Lifecycle Management, Design C[...]

Senior Device Engineer – Electromechanical Combination Products

Location:

Thousand Oaks, CA. 91320

Employment Type:

Contract

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

Posting Date: 04/30/26

Pay Rate: $44 - $48.50/hour W2

Job Description

Ideal candidate:
Seeking candidates with experience in combination products, electromechanical systems, or medical devices, a background in pharma, and hands‑on expertise in design control and testing.

Our client is seeking a contract electromechanical combination product Device Engineer. The Device Engineer will participate in design development and lifecycle management‑related activities for commercialized drug delivery devices and devices under development.

Top Must Have Skills
  • Lifecycle Management Experience with electromechanical platforms
  • Root Cause Analysis and Technical Problem Solving
  • Proven success in cross‑functional engagement and being a team player
  • Nice to have:
    Early device development experience
Day‑to‑Day Responsibilities
  • Provide ongoing lifecycle management (LCM) support for electromechanical combination products, including post‑market activities, design improvements, and cross‑functional issue resolution to ensure product reliability and compliance.
  • Lead complaint investigations by performing detailed failure analysis, identifying root causes, and developing data‑driven action plans in collaboration with quality, manufacturing, and regulatory teams.
  • Drive and manage quality system processes including CAPAs, deviations, and change controls, ensuring timely closure, robust documentation, and alignment with regulatory and internal requirements.
  • Collaborate closely with external suppliers to support LCM activities, including issue resolution, component updates, root cause analysis, CAPAs and continuous improvement initiatives to maintain supply continuity and product performance.
  • Manage change assessments driven by internal and external changes during the life cycle of the combination product.
  • Participate in and support cross‑functional design reviews for combination product development.
  • Provide design verification support for combination products, ensuring compliance with Quality System Requirements, Design Control (21 CFR 820.30), and ISO 13485.
  • Lead and execute on‑site testing and verification activities for electromechanical delivery systems and related platforms.
  • Develop, review, and execute test protocols, reports, and technical documentation in accordance with design control and regulatory expectations.
  • Perform data verification, analysis, and traceability reviews to ensure product performance meets user needs and design inputs.
  • Partner cross‑functionally with R&D, Human Factors, Quality, Regulatory, and Manufacturing teams to drive design robustness, risk mitigation, and design transfer readiness.
Basic Qualifications
  • Doctorate degree OR Masters degree and 2 years of experience OR Bachelors degree and 4 years of experience OR Associates degree and 8 years of experience OR High school diploma / GED and 10 years of experience
Preferred Qualifications
  • Master’s or Bachelor’s Degree in Engineering Discipline (Mechanical, Biomedical, Electrical) with 3‑5 years (or 2 years with Masters) of professional experience in a highly regulated environment (strong preference for medical device, biopharma and/or combination product experience).
  • Experience with electromechanical systems, injection devices, medical devices or delivery platforms preferred.
  • Demonstrated expertise in lifecycle management, data analysis, and protocol/report generation under design control.
  • Strong understanding of materials coordination, supplier interaction, and lab testing logistics.
  • Proven ability to work in cross‑functional project teams, communicate technical results clearly, and lead execution to meet program milestones.
  • Working proficiency in statistical analysis software (Minitab).
  • Smartsheets proficiency is a plus.
  • Ability to work independently and dynamically across functional teams.
  • Excellent written and verbal communication skills.
  • Must be capable of working on multiple projects in a deadline‑driven environment.
  • The position is designed for candidates at a mid‑career stage, with scope and responsibilities aligned to that level of experience.
#J-18808-Ljbffr
Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary