I

Project Engineer

Accepting applications

IntePros · Audubon, PA

Full-Time Entry aiateddrganrf
Posted
19 Apr
Category
Test
Experience
Entry
Country
United States
IntePros is currently looking for a Project Engineer to join one of our growing Medical Device clients in Audubon, PA. The Project Engineer will be responsible for all engineering functions of their product lines. This includes bringing a product from idea/concept through design, prototyping, development testing, design verification and validation, manufacturing, FDA approvals, product introduction and post introduction monitoring. The Project Engineer will work with surgeons and all other functions of the company to ensure high quality and on-time product introductions.

Project Engineer Responsibilities

Obtains market feedback from surgeons and other customers to determine functional and design specifications for new product development
Creates and maintains project plans and FDA complaint Design history Files (DHF) for each project
Manages all aspects of assigned projects to ensure timely completion of tasks while remaining in full compliance with client quality system and other applicable regulatory bodies
Designs and develops instruments and implants using Pro/E and SolidWorks software
Partners with in-house prototype shop and outside vendors for rapid prototyping and evaluation
Performs design verification and validation activities to ensure designs meet specifications
Collaborates with marketing and product managers to develop forecasts and market plans
Assists in the writing of regulatory applications to the FDA and other regulatory bodies
Partners with the operations department to setup manufacturing and/or purchasing as appropriate for each project
Participates in product introductions through sales training, customer calls/visits, etc.
Maintains diligent post introduction monitoring to address and customer requests for changes
Researches industry and direct competitors on an ongoing basis to ensure that client has cutting edge technology in all markets entered
Adheres to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech Code, and all other company policies.
Ensures Compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to your role
Represents the company in a professional manner and uphold the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties
Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.

Project Engineer Qualifications

3-7 years experience in mechanical design engineering; Medical device experience strongly preferred
Bachelor’s Degree in Mechanical Engineering, Bioengineering, Biomedical Engineering or a similar degree
Proficiency in Pro/E and/or SolidWorks software for design and drafting
Well organized, detail oriented, and team player capable of working in a deadline driven environment
Experience in preparing reports and managing project budgets
Strong knowledge of Microsoft Office
Ability to attend surgeries and/or labs

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