Mechanical Engineer II in Mansfield Job Mansfield area,Massachusetts USA,Engineering

Job Summary and Objective:

The Mechanical Engineer II will collaborate with team members to design and refine cutting‑edge medical devices, contributing to product testing, validation, and optimization. Working closely with management, quality assurance, supply chain, and engineering teams, the Mechanical Engineer will oversee all stages of product development, encompassing mechanical design, materials sourcing, prototype fabrication, and the planning and implementation of characterization tests. Responsibilities will also include the development of test protocols, active participation in product testing, and the preparation of comprehensive test reports.

Essential Duties and Responsibilities:

Collaborate in the mechanical design and development of diverse medical devices.
Create robust solid models, drawings, and detailed specifications.
Conduct thorough characterization and environmental tests to validate the design and performance of devices.
Interface with suppliers to select critical components and qualify tools.
Strategize and coordinate activities to achieve results and meet crucial deadlines, translating client requirements into project milestones.
Coordinate closely with operations and quality teams to ensure adherence to design specifications.
Ensure engineering projects and processes align with the organization’s policies and objectives.
Engage in cross‑departmental project discussions to identify and resolve design‑related issues.
Prepare and review necessary documentation for product feasibility and design, ensuring compliance with client and industry specifications.
Identify and mitigate risk associated with device functionality, reliability, safety, COGs, and manufacturing scalability.
Design and evaluate feasibility of improved device components, subsystems, and assembled products.

Supervisory Responsibilities:

Does not regularly supervise employees.
May oversee other employees for isolated or specific tasks.

Required Qualifications and

Work Experience:

Bachelor's Degree in Mechanical Engineering (B.S., M.E.)
5+ years of experience in design engineering
Proficiency in Solid Works design software
Demonstrated leadership in developing new products, technologies, and associated processes
Experience in injection molding, metal forming, welding, and other metal and plastic joining methods
Experience with design for automation
Excellent communication skills
Proficient in Microsoft Project and Microsoft Office suite
Working knowledge of FDA Quality System Regulation (QSR) and ISO 13485 guidelines related to Design Controls
Strong written and verbal communication skills
Ability to work independently with minimal supervision and consistently achieve goals.

Physical Demands:

Full range of motion for wrist, hand, and finger dexterity
Comfortable with prolonged sitting and working at a computer
Proficient in an engineering lab environment
Working in a cleanroom environment

Benefits Offered:

Medical, Dental, Vision Insurance
401(k)
Paid Time Off
Long-Term & Short-Term
Life Insurance
10 Paid Holidays
Additional Voluntary Benefits

8:00am - 5:00pm

#J-18808-Ljbffr