Principal R&D Sustaining Engineer
Job in
Westborough, Worcester County, Massachusetts, 01581, USA
Listed on 2026-07-10
Listing for:
Olympus Corporation of the Americas
Full Time
position Listed on 2026-07-10
Job specializations:
-
Engineering
Quality Engineering, Biomedical Engineer, Product Engineer, Manufacturing Engineer
Job Description & How to Apply Below
Location:
Massachusetts, Westborough*
* ** Workplace Flexibility:
Hybrid*
* ** _For more than 100 years, Olympus has focused on making people's lives healthier, safer and more fulfilling. _*
* ** __*
*
Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can fulfill their desires, dreams, and lives.
Our five Core Values empower us to achieve Our
Purpose:
** Patient Focus, Integrity, Innovation, Impact and Empathy.*
* Learn more about Life at Olympus:
.
** Job Description*
* The Principal Engineer is responsible for performing and/or leading all aspects of Sustaining including technical planning, feasibility studies, device development, investigations and corrective actions, cost reductions, verification, and validation activities. The primary responsibility of the position is the technical maintenance of the Design History File and Technical Files post launch. They must fully understand medical device design control requirements and be able to effectively manage a project and work effectively in a cross functional team.
May serve as a core or extended team member on projects. Maintains detailed documentation throughout all phases of research and development.
May provide leadership and direction to Engineering Technicians and mentor less experienced engineers within and across OSTA sites in best practices for the use of engineering tools and methods.
** Job Duties*
* + Provides technical leadership on Sustaining / Systems projects and/or development efforts.
+ Accountable for all aspects of product development activities and product Design History File, such as; requirements creation/documentation, ideation / prototyping, design / development, technical risk mitigation, verification testing and reports, design validation studies, risk management documentation, design reviews, and supports the compilation of documents to enable regulatory submissions.
+ Develops engineering solutions, investigates competing technologies, and collaborates with Olympus Patent Attorneys to secure a strong IP portfolio.
+ Directs or performs design analysis, such as tolerance stack-ups, strength of materials, risk analysis, and statistical evaluations.
+ Ensures product designs are cost effective, manufacturable, and products are tested through well thought out verification plans to ensure a high degree of product quality and reliability.
+ Consults with the Sales, Marketing, and clinicians to define and specify product user requirements.
+ Manages, directs and supports suppliers involved in product development and ongoing production. This includes outside design and/or development/manufacturing partners.
+ Helps prepare and acts as a consultant to marketing on technical brochures, training programs, and technical presentations to customers and the sales force.
+ Drives Design History File remediation efforts and CAPA projects as needed.
+ Supports engineering leadership as required.
** Job Requirements*
* *
* Required:
*
* + Bachelor's degree in Biomedical, Mechanical Engineering, Electrical Engineering or similar.
+ Minimum of 9 years of related experience or 8 years with MS or 5 years with PhD.
+ Ability to effectively work within a requirements management system.
+ Previous experience in design, development, and sustaining of Medical Devices.
+ Must have extensive working knowledge of, and experience in applying / developing products in compliance with FDA and international requirements, including 820-CFR, ISO
14971, IEC
60601, GMP and other standards as they relate to the design and manufacture of medical devices.
+ Proficient in Microsoft Windows Office applications including MS Outlook, MS Powerpoint, MS Project, Visio, etc.
+ Solidworks working knowledge.
+ Proficient in the creation and critical review of engineering drawings including geometric dimensioning and tolerancing and tolerance analysis.
+ Knowledge of common manufacturing methodologies, technologies, and materials, such as; injection molded part design, common materials employed in medical devices, and other manufacturing processes.
+ Must be able to solve complex and/or…
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