Senior Device Engineer
Job in
Billerica, Middlesex County, Massachusetts, 01821, USA
Listed on 2026-10-11
Listing for:
ClinLab Solutions Group
Full Time
position Listed on 2026-10-11
Job specializations:
-
Engineering
Quality Engineering, Mechanical Engineer, Manufacturing Engineer
Job Description & How to Apply Below
Middlesex County, Massachusetts
Summary:
This role focuses on providing mechanical and electromechanical engineering support for both existing and new medical device projects, ensuring product quality, compliance, and continuous improvement.
Responsibilities:- Support existing medical products by investigating and analyzing product issues, determining root causes, and implementing effective resolutions to meet customer requirements.
- Prepare and maintain comprehensive product documentation, including specifications, bills of material, hazard/risk analyses, test procedures, validations, and procedures, while supporting suppliers and contract manufacturers.
- Conduct mechanical tests and experiments to ensure designs comply with industry standards, safety margins, reliability goals, and relevant international standards.
- Participate in project teams, assisting with project planning, estimation, scheduling, tracking, and reporting for engineering projects.
- Prioritize quality system requirements in all activities, including design, development, validation protocols, and risk assessments.
- Develop specifications, packaging, labeling, and all associated design control documents in accordance with project, industry, and regulatory requirements.
- Contribute to regulatory submissions and generate ideas or intellectual property submissions as needed.
- Provide training or direction to technicians, manufacturing personnel, or suppliers, and perform other duties as assigned.
- BS in Mechanical Engineering preferred;
Associate’s degree in Mechanical Engineering or relevant experience will be considered. - 7 years of experience in the medical device industry required.
- Ability to interpret and resolve technical and design issues required.
- Familiarity with QSR/GMP regulations required.
- Experience with Microsoft Office Tools and Solid Works required.
- Pharmaceutical industry experience is a plus.
- Ability to operate production equipment, hand tools, and computer/office equipment.
- Physical ability to lift and move heavy boxes/equipment up to 70 lbs, and work in various environments including office, lab, manufacturing, and maintenance areas.
Manufacturing & Technical Operations
Position Requirements
10+ Years
work experience
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