Senior Staff Mechanical Engineer

6 days ago

Pittsburgh, Pennsylvania, United States Philips Full time
Job TitleSenior Staff Mechanical EngineerJob Description

Senior Staff Mechanical Engineer

The Senior Staff Mechanical Engineer will operate as a leader and individual technical contributor, responsible for contributions towards and oversight of key Sleep Therapy product development projects from a mechanical engineering perspective.

Your role:

  • Conceptual design, prototyping, testing, and maintenance of electro-mechanical devices used to treat obstructive sleep apnea.
  • Developing of mechanical components, assemblies, plastic part design and high-volume manufacturing, injection molding
  • Coordinating and driving project activities from the mechanical engineering focus, ensuring and advancing the team's adherence to good engineering practices, procedures and Quality System requirements.
  • Actively scheduling, organizing, and leading project meetings & design reviews for product concepts, solutions, results, and status.
  • Remain agile personally and within the team to adjust and respond to the needs of supporting product development and the demands of the business.
  • Maintaining and improving the quality position of the mechanical engineering team's deliverables and the overall business unit's products.
  • Composure, conflict management, timely decision making, listening skills, self-motivation, and perseverance are all requirements of this position.
  • Acting as a leader within the engineering team, ensuring active participation in activities that enhance the engagement of the overall team.
  • Mentor engineers on technical issues, problem solving strategies, and engineering principles.
  • Reporting to the Director of Sleep Therapy & Diagnostics Engineering, you will collaborate with a cross functional team of engineers and specialists throughout the Sleep & Respiratory Care organization.
  • This Hybrid, Pittsburgh, PA based role may require travel up to 10%.

You're the right fit if:

  • You have a minimum of 10 years combined experience in product and process development within a regulated environment (FDA regulated medical device preferred), with a focus on the design/development of mechanical components, assemblies, plastic part design, high-volume manufacturing and injection molding.
  • You have proven expertise in solid modeling (CREO), CAE/FEA for structural, molding, thermal, or fluid flow (MoldFlow/ANSYS).
  • You have strong experience developing performance requirements, design documents, implementation and Design V&V processes and testing.
  • You're experienced working with consumer products and marketing teams, contributing a technical voice to determining new product value propositions.
  • You have extensive experience developing injection-molded plastic parts, including material selection, and component over molding as well as a design background, preferably in the medical device industry.
  • You've displayed a strong understanding of high-volume, plastic part production qualification requirements (such as IQ/OQ/PQ) and quality assurance/regulatory requirements.
  • You're able to understand dimensional tolerances, manufacturing capabilities and target costing, harmonizing designs with procurement engineers to ensure robust, successful supply chains.
  • You have demonstrated success in leading technical teams, with the ability to work on multiple projects.
  • You have proven creativity, strong technical judgment and the interpersonal skills required for the successful completion of multiple projects.
  • You have a minimum of a Bachelor of Science in Mechanical Engineering, Plastics Engineering, or Engineering Technology (Required). Master of Science-Desired.
  • You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.
  • US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
  • Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Pittsburgh, PA.

About Philips:

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

  • Learn more about our business.
  • Discover our rich and exciting history.
  • Learn more about our purpose.
  • Read more about our employee benefits.

If you're interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.

#LI-PH1

This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.

Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.

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