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Senior Device Engineer – Electromechanical Combination Products; Lifecycle Management, Design Control, CAPA JP

Job in Newbury Park, Ventura County, California, 91320, USA
Listing for: 3 Key Consulting
Full Time position
Listed on 2026-08-24
Job specializations:
  • Engineering
    Medical Device Industry, Biomedical Engineer, Quality Engineering, Systems Engineer
Salary/Wage Range or Industry Benchmark: 44 - 48 USD Hourly USD 44.00 48.00 HOUR
Job Description & How to Apply Below
Position: Senior Device Engineer – Electromechanical Combination Products (Lifecycle Management, Design Control, CAPA) - (JP15626)
Location: Newbury Park

Senior Device Engineer – Electromechanical Combination Products

Senior Device Engineer – Electromechanical Combination Products (Lifecycle Management, Design Control, CAPA)

Location:

Thousand Oaks, CA. 91320

Employment Type:

Contract

Business Unit:
Electromechanical Platform

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

Pay Rate: $44 - $48/hour W2 with benefits

Notes: 3-5 days onsite depending on business needs
- Standard hours
- Local Candidates Only.

3 Key Consulting is hiring a Senior Device Engineer – Electromechanical Combination Products for a consulting engagement with our direct client, a leading global biopharmaceutical company.

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.

Why is the Position Open?

Supplement additional workload on team

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 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…
Position Requirements
10+ Years work experience
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