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Sr. Manager, R&D

Getinge
life insurance, vision insurance, paid time off, long term disability, tuition reimbursement, 401(k)
United States, Massachusetts, Boston
May 19, 2026


With a passion for life

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers.

Are you looking for an inspiring career? You just found it.

This role is open to US based candidates

Paragonix Technologies markets organ transportation devices that safeguard organs during the journey between donor and recipient patients. Our devices incorporate clinically proven and medically trusted hypothermic preservation techniques in a novel suspension system to provide unprecedented physical and thermal protection. Our product portfolio spans cardiac, thoracic, and abdominal preservation devices to improve donor organ quality and extend donor organ transport time.Paragonix also markets transplant services and organ screeningto the transplant community.

Our company provides the leading commercial system for heart preservation and transportation as well as transplant systems for kidney, lungs, liver and pancreas. As we grow, we are looking to add a Sr. R&D Manager reporting to the Sr. R&D Director. This position will be responsible for collaborating with cross functional departments to align R&D effort with business goals. This role is crucial to continue fostering innovation and ensuring continued success in advancing transplant care.

Job Responsibilities and Essential Duties




  • Lead the design, prototyping, and evaluation of innovative transplant devices, integrating advanced technologies to enhance organ preservation methods.
  • Assess potential intellectual property opportunities related to organ transplantation and preservation.
  • Oversee projects from concept through feasibility, verification, validation, and design transfer to manufacturing, ensuring compliance with ISO 13485 and FDA regulations.
  • Partner with marketing, regulatory affairs, quality assurance, and manufacturing teams to ensure regulatory compliance and commercial feasibility.
  • Review design outputs (e.g., schematics, CAD models, PCB layouts) and manage design controls to minimize risks (ISO 14971).
  • Recruit, mentor, and manage a team of high-performing engineers, fostering a culture of innovation and critical thinking.
  • Manage competing priorities and organizational change by clarifying tradeoffs, communicating decisions, and maintaining strong team engagement.
  • Oversee relationships with external vendors, consultants, and partners.



Required Knowledge & Skills




  • Demonstrated basic understanding of medical device regulatory standards and frameworks, including ISO 14971 for risk management throughout the product lifecycle, IEC 62366 and FDA human factors guidance for usability engineering and use-related risk analysis, ISO 10993 for biocompatibility and biological evaluation of medical devices and materials, and IEC 60601 standards for electrical safety and essential performance of medical electrical equipment.
  • Bachelor's degree in engineering (Mechanical, Biomedical or related field). Master's degree preferred.
  • Minimum of 8 years of experience in engineering roles, with at least 3 years in a leadership or managerial position within the medical device industry.
  • Demonstrate understanding of design principles and requirements for injection molding and other plastic manufacturing methods.
  • Demonstrated ability to lead engineering teams and direct reports through various stages of product development process
  • Self-motivated with ability to think strategically and solve complex problems
  • Interpersonal skills to communicate, advise, negotiate or influence others, as well as build productive working relationships in various settings.
  • Previous CAD experience required. Solid Works preferred.



General Responsibilities:




  • Onsite personnel
  • Must be willing to travel 15%



US BASED SALARY - The minimum base salary for this position is $160,000 and the maximum salary is $175,000 plus 10% in annual bonus.

About us

With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.

Benefits at Getinge:

At Getinge, we offer a comprehensive benefits package, which includes:



  • Health, Dental, and Vision insurance benefits
  • 401k plan with company match
  • Paid Time Off
  • Wellness initiative & Health Assistance Resources
  • Life Insurance
  • Short and Long Term Disability Benefits
  • Health and Dependent Care Flexible Spending Accounts
  • Commuter Benefits
  • Parental and Caregiver Leave
  • Tuition Reimbursement



Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law.Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.


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