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Sr Product Development Engineer--Interventional Devices (Hybrid)

AngioDynamics

112k - 130k USD/year

Office

Marlborough, MA, US

Full Time

JOIN A TEAM COMMITTED TO IMPROVING PATIENT CARE

It takes a team of talented people to become one of the world’s leading providers of innovative medical devices.


AngioDynamics is dedicated to improving patient outcomes by focusing on the development of disruptive and differentiated technologies that address unmet patient needs and supporting professional healthcare providers around the world in the delivery of high-quality patient care.


We accomplish this through:

• A Commitment to the Highest Standards of Quality
• Relentless Innovation
• Operational Excellence

Our employees receive the highest level of training and endeavor to be the best and the brightest in the medical device industry.


We are pleased to offer a comprehensive benefit plan that supports the overall health and wellness needs of our employees and their families.


JOB SUMMARY– To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.

The Sr R&D Engineer is responsible for leading the technical aspects for our commercialized Interventional Devices product portfolio. This role is focused on sustaining engineering efforts to ensure continued performance, compliance, and customer satisfaction. Key responsibilities include design maintenance, risk management, and cross functional support for quality, regulatory and supply chain issues.

Essential Duties and Responsibilities

Serve as the technical lead for sustaining engineering and marketing support activities related to our Interventional Devices portfolio

Own and execute design updates, engineering assessments, and documentation revisions in accordance with quality and regulatory standards

Collaborate with cross-functional teams (Quality, Regulatory, Manufacturing, Supply Chain) to address product issues, resolve complaints, and manage component obsolesces

Complies and analyzes, operational, test and research data to establish technical specifications for designing or modifying products, processes and materials

Successfully completes complex engineering work in one or more of the following: technology development, product design and development, test of materials or products, preparation of specifications, process study, research investigation (animal and clinical studies), and report preparation

Use fundamental PD/DFM tools to reduce variation and achieve capable processes with high production yields where required

Perform process optimization through DOEs, DCMs and process capability studies, as required

Selects techniques to solve complex problems and make sound design recommendations

Summarizes, analyzes and draws conclusions from complex test results

Designs and prepares complex reports to communicate results to technical community

Designs and coordinates complex engineering tests and experiments

Interfaces with Physicians/Cath Lab personnel to obtain feedback on concepts and performance of devices

Translates customer needs into product requirements and design specifications


Write, execute and review validation protocols and reports when appropriate

Conduct test method development as required by project teams

Stay current with and ensure appropriate compliance with SOP’s on all projects

Provide timely responses to the Corrective Action/Preventive Action (CAPA) program as required

Provide support as required to safety, ISO, FDA, corporate and internal audits

May perform other duties as assigned


QUALIFICATIONS–The requirements listed below are representative of the knowledge, skill or ability required.

Education and Experience

Bachelor’s Level of Degree in the Engineering/Technical field of study

Equivalent work related experience acceptable in lieu of degree Yes No

8 years of demonstrated experience in Engineering or related field

Experience in the medical device industry


Skills/Knowledge

Prior experience with SolidWorks and Minitab software a plus

Proven statistical analysis on product and process capabilities

Excellent attention to detail and documentation practices

Ability to manage multiple tasks in a fast-paced, compliance-driven environment

Proficient in the following computer software applications: Microsoft Office

Exceptional interpersonal skills.

Strong organizational skills.

Strong communication skills (written and verbal).

Ability to effectively communicate both internally and externally.

Ability to read and interpret documents such as safety rules, operating and maintenance, instructions, and procedure manuals. Ability to write routine reports and correspondence.


All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other legally protected status.

The Company will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant.

AngioDynamics does not accept resumes or candidate submissions from third-party recruiters and/or vendors who are not expressly under current written contract.

Your ultimate salary may vary depending on your job-related skills, knowledge, and experience.

Sr Product Development Engineer--Interventional Devices (Hybrid)

Office

Marlborough, MA, US

Full Time

112k - 130k USD/year

August 8, 2025

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AngioDynamics

angiodynamics