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Medical Device Product Development Jobs in Rochester, NY

... medical device organization as it evolves toward pharmaceutical and combination product development. This role provides hands-on regulatory leadership for FDA submissions, clinical studies, and ...

Regulatory Affairs Lead

Rochester, NY · On-site

$125K - $130K/yr

... medical device organization as it evolves toward pharmaceutical and combination product development. This role provides hands-on regulatory leadership for FDA submissions, clinical studies, and ...

... are and medical device environment. The ideal candidate will have strong leadership skills ... Experience working in cross-functional environments supporting product development and ...

Medical Sales - DME

Rochester, NY · On-site

$85K - $115K/yr

Understand and execute sales territory management and customer development. * Establish and ... Some education or knowledge of medical equipment/device and healthcare products * Demonstration of ...

Medical Sales - DME

Rochester, NY · On-site

$85K - $115K/yr

Understand and execute sales territory management and customer development. * Establish and ... Some education or knowledge of medical equipment/device and healthcare products * Demonstration of ...

Project Manager

Newark, NY · On-site

$95K - $115K/yr

Experience managing new product development projects. * Experience within battery, electronics, aerospace, defense, medical device, or other highly regulated manufacturing environments. * Familiarity ...

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Medical Device Product Development information

See Rochester, NY salary details

$41.9K

$125.3K

$142.6K

How much do medical device product development jobs pay per year?

As of Aug 8, 2026, the average yearly pay for medical device product development in Rochester, NY is $125,295.00, according to ZipRecruiter salary data. Most workers in this role earn between $113,000.00 and $141,100.00 per year, depending on experience, location, and employer.

What is a medical device product development?

A Medical Device Product Development job involves designing, testing, and bringing medical devices to market while ensuring compliance with regulatory standards. Professionals in this role work with cross-functional teams, including engineering, regulatory affairs, and manufacturing, to develop safe and effective healthcare solutions. They oversee the entire product lifecycle, from concept and prototyping to clinical validation and commercialization. Strong knowledge of FDA, ISO, and other regulatory requirements is essential.

What are some typical challenges faced in medical device product development roles?

Professionals in Medical Device Product Development often encounter challenges such as navigating complex regulatory requirements, managing cross-functional project teams, and ensuring that products meet both clinical needs and quality standards. Balancing innovative design with safety and compliance can require careful planning and solid problem-solving skills. Additionally, adapting to shifting project timelines and incorporating stakeholder feedback are common aspects of the job. Overcoming these challenges is rewarding and helps ensure the delivery of safe, effective devices to patients and healthcare providers.

What are the key skills and qualifications needed to thrive in medical device product development?

To thrive in Medical Device Product Development, you need a strong background in engineering or life sciences, product design, and an understanding of regulatory requirements like FDA and ISO standards. Proficiency with CAD software, project management tools, and knowledge of quality management systems (QMS) is commonly required, along with certifications such as Six Sigma or PMP being beneficial. Strong problem-solving abilities, collaboration skills, and effective communication are key soft skills for this role. These skills are important to ensure that devices are developed safely, efficiently, and in compliance with industry regulations while fostering innovation and teamwork.

What are the most commonly searched types of Medical Device Product Development jobs in Rochester, NY? The most popular types of Medical Device Product Development jobs in Rochester, NY are:
What job categories do people searching Medical Device Product Development jobs in Rochester, NY look for? The top searched job categories for Medical Device Product Development jobs in Rochester, NY are:
Infographic showing various Medical Device Product Development job openings in Rochester, NY as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $125,295 per year, or $60.2 per hour.

Research Fellow, Medical Device Toxicologist

Bausch & Lomb GmbH

Rochester, NY • On-site

$150 - $200/hr

Other

Medical, Dental, Life, Retirement, PTO

Posted 3 days ago

New


Job description

The Research Fellow – Medical Device Toxicologist will provide cross‑functional preclinical medical‑device expertise supporting internal and external stakeholders on biocompatibility and related focus areas for medical device development, product expansion, and maintenance.

Responsibilities
  • Manage a team responsible for medical device biocompatibility support
  • Lead project strategies, risk assessments, biocompatibility evaluation plans, and reports for medical devices
  • Ensure that development and execution of non‑clinical strategies align with product development, life‑cycle management activities, and regulatory expectations and milestones
  • Ensure that essential non‑clinical data are obtained and effectively presented for successful clinical development, regulatory and quality compliance, market launch, and maintenance of business
  • Coach and mentor junior staff
  • Maintain deep understanding of medical‑device relevant standards and stay abreast of changes to applicable industry practice and guidance documents
  • Implement new and revised standards into product development projects and assess impact on existing products as appropriate
  • Author and review the department’s technical documents as needed
  • Manage interactions with other functions (Product Development, Clinical Development, Analytical Chemistry, Regulatory, Quality, Compliance)
  • Liaise with company international offices on non‑clinical safety matters for country‑specific submissions/registrations and maintenance of business activities
  • Develop and maintain department best practices and processes
Requirements
  • Ph.D. in Toxicology or related discipline
  • 12+ years of relevant medical‑device industry experience
  • Experience managing a team
  • DABT preferred
  • Ophthalmic medical‑device experience a plus
Benefits
  • Medical, dental, eye‑health, disability and life insurance (beginning on your hire date)
  • 401(k) plan with company match and ongoing contributions
  • Paid time off – vacation (3 weeks prorated upon hire), floating holidays, and sick time
  • Employee stock purchase plan with company match
  • Employee incentive bonus
  • Tuition reimbursement (select degrees)
  • Ongoing performance feedback and annual compensation review

Location: US – Rochester, NY (GEHC)

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

Starting pay for this role is between $150,000.00 and $200,000.00. The actual base salary offered may depend on a variety of factors.

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