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Senior Mechanical Engineer
Job in
Scranton, Lackawanna County, Pennsylvania, 18512, USA
Listed on 2026-05-31
Listing for:
United Pharma Technologies Inc
Full Time
position Listed on 2026-05-31
Job specializations:
-
Engineering
Product Engineer, Mechanical Engineer
Job Description & How to Apply Below
We are seeking an experienced Senior Mechanical Engineer with a strong background in medical device product development and mechanical design. The ideal candidate will bring recent experience working with DePuy Synthes, preferably within the Spine, Trauma, or CMF (Cranio-Maxillofacial) product lines. This role requires expertise in CAD design, PLM systems, GD&T, and product development within a regulated medical device environment.
Key Responsibilities- Support the design, development, and engineering of medical device products from concept through commercialization.
- Develop and maintain mechanical designs using Creo/Pro Engineer (Pro/E) CAD software.
- Utilize Windchill PLM for product lifecycle management, engineering documentation, and change control activities.
- Apply GD&T principles to product design, drawings, and manufacturing requirements.
- Collaborate with cross-functional teams including R&D, Quality, Manufacturing, and Product Development.
- Ensure compliance with design control, documentation, and regulatory requirements in a medical device environment.
- Contribute to technical problem-solving, design reviews, and continuous product improvement initiatives.
- Bachelor’s degree in Mechanical Engineering or related engineering discipline.
- Recent experience with DePuy Synthes (preferred within the last 4–5 years).
- Hands‑on experience supporting Spine, Trauma, or CMF medical device product lines.
- Strong working knowledge of Windchill PLM systems.
- Proficiency in Creo / Pro Engineer (Pro/E) CAD software.
- Proven experience in mechanical design and product development.
- Strong understanding and practical application of GD&T (Geometric Dimensioning & Tolerancing) principles.
- Experience working within a regulated medical device environment.
- Strong understanding of design controls, documentation practices, and engineering change management.
- Ability to work effectively with cross-functional engineering and product development teams.
Position Requirements
10+ Years
work experience
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