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Medical Device Product Development Manager Jobs in Indiana

... innovative medical device products in order to further Zimmer Biomet's mission and grow Zimmer ... management documentation as part of the product development process in compliance with Zimmer ...

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Coordinate with production, quality, shipping, purchasing, and management to support customer needs ... Experience in medical device, healthcare, manufacturing, distribution, or regulated industries.

... for the medical device industry. From concept through high-volume production, our teams work ... Lead the strategy, development, implementation, and lifecycle management of sterile packaging ...

... for the medical device industry. From concept through high-volume production, our teams work ... This role partners cross-functionally with Regulatory, Product Development, Operations, Supply ...

Manager, Product Development

Indianapolis, IN ยท On-site

$109K - $136K/yr

Reporting to the Director, Nuclear Manufacturing, the Manager, Product Development, is responsible ... Medical, dental and vision coverage * Paid time off plan * Health savings account (HSA) * 401k ...

... for the medical device industry. From concept through high-volume production, our teams work ... This role partners cross-functionally with Regulatory, Product Development, Operations, Supply ...

Showing results 21-40

Medical Device Product Development Manager information

See Indiana salary details

$38K

$121.1K

$138.5K

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

As of Aug 9, 2026, the average yearly pay for medical device product development manager in Indiana is $121,130.00, according to ZipRecruiter salary data. Most workers in this role earn between $109,600.00 and $137,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a medical device product development manager, and why are they important?

To thrive as a Medical Device Product Development Manager, you need expertise in engineering or life sciences, experience with product lifecycle management, and knowledge of regulatory requirements, often supported by a relevant degree. Familiarity with CAD software, project management tools, and compliance systems such as ISO 13485 or FDA regulations is typically required. Strong leadership, cross-functional communication, and problem-solving skills help drive innovation and align diverse teams. These competencies are vital to ensure products are developed efficiently, safely, and in compliance with industry standards.

How does a medical device product development manager typically collaborate with cross-functional teams during the development process?

A Medical Device Product Development Manager works closely with cross-functional teams, including engineering, regulatory affairs, quality assurance, marketing, and clinical experts, to ensure that product requirements are met throughout each development phase. They facilitate regular meetings to align on project milestones, address potential risks, and incorporate feedback from various stakeholders. This collaborative environment helps ensure that the final product complies with regulatory standards and meets market needs, making strong communication and project management skills essential in this role.

What is the difference between Medical Device Product Development Manager vs Medical Device Quality Assurance Specialist?

AspectMedical Device Product Development ManagerMedical Device Quality Assurance Specialist
CredentialsEngineering degree, certifications like PMP or PDMAQuality assurance certifications like CQE, ISO auditor
Work EnvironmentDesign teams, R&D, cross-functional project groupsQuality labs, compliance departments, manufacturing oversight
Industry UsageLeading product development from concept to launchEnsuring products meet quality and regulatory standards

The Medical Device Product Development Manager focuses on designing and developing new medical devices, managing cross-functional teams, and bringing products to market. In contrast, the Medical Device Quality Assurance Specialist ensures that products meet quality standards and regulatory requirements throughout the development and manufacturing process. Both roles are essential in the medical device industry but serve different functions in product lifecycle management.

What does a medical device product development manager do?

A Medical Device Product Development Manager oversees the entire process of bringing a medical device from the concept stage to market launch. They coordinate cross-functional teams, manage timelines, ensure compliance with regulatory standards, and oversee testing and validation of products. Their responsibilities also include working with engineers, designers, and regulatory specialists to ensure the device meets safety, efficacy, and user needs. Ultimately, they play a critical role in ensuring that new medical devices are developed efficiently, safely, and in compliance with industry standards.
What cities in Indiana are hiring for Medical Device Product Development Manager jobs? Cities in Indiana with the most Medical Device Product Development Manager job openings:

Product Development Engineer

PinnaclePartners

Indianapolis, IN โ€ข On-site

$90K - $105K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 hours ago

Posted today


Job description

Job Description About the Role Pinnacle Partners is recruiting for a Product Development Engineer on behalf of a client in Indianapolis, Indiana. We are seeking an innovative engineer who enjoys taking products from concept through commercialization while working in a collaborative, hands-on environment. This role offers the opportunity to lead new product development projects, build and test prototypes, collaborate across multiple departments, and help bring innovative medical devices to market.

Key Responsibilities: Lead and own new product development projects from concept through commercialization. Manage approximately 70% new product development and 30% sustaining engineering initiatives. Translate customer, clinician, and product management needs into engineering requirements and product specifications.

Design and model components using CAD software (SolidWorks preferred). Build and evaluate functional prototypes using hands-on fabrication techniques. Select materials and components for prototypes and production products.

Develop verification test methods, protocols, and validation plans to ensure products meet design requirements. Conduct product testing, analyze results, and recommend design improvements. Create and maintain Design History Files (DHF), engineering drawings, specifications, test reports, and technical documentation.

Perform product risk analysis and implement mitigation strategies throughout the product development lifecycle. Support Design for Manufacturability (DFM) and manufacturing transfer activities. Collaborate with Manufacturing, Quality, Product Management, Marketing, Sales, Customer Service, Clinical teams, and international engineering teams.

Support patent activities by providing engineering drawings and technical documentation. Manage prototype and laboratory equipment used for product development and testing. Requirements: Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Industrial Design, Design Engineering, or a related engineering discipline.

Experience leading products through the complete product development lifecycle from concept through production. Hands-on prototyping and research & development experience. Experience with product verification, validation, product testing, and test method development.

Strong understanding of Design for Manufacturability (DFM). Experience creating engineering documentation, technical reports, and Design History Files (DHF). CAD proficiency, preferably with SolidWorks.

Strong analytical, problem-solving, and communication skills. Ability to collaborate effectively with cross-functional teams throughout product development. Preferred: Medical device or other FDA-regulated product development experience.

Knowledge of ISO 13485 and regulated product development processes. Experience with patent support and engineering documentation. Exposure to RF welding or sewing technologies.

Experience supporting new product launches and sustaining engineering projects. Benefits Overview: Competitive salary of approximately $90,000-$105,000 Medical, dental, and vision insurance. Company-paid life insurance and short-term disability.

Long-term disability coverage. 401(k) with employer match. Health Savings Account (HSA) employer contribution.

Wellness reimbursement up to $250 annually. Childcare reimbursement up to $250 annually. Paid vacation and merit increase opportunities.

Opportunity to work on innovative medical devices while owning projects from concept through commercialization. Collaborative engineering environment with hands-on prototype development and long-term growth opportunities. Explore More Engineering Opportunities This role falls within our Engineering/Manufacturing division, where we specialize in placing professionals in areas such as: Mechanical/Electrical Engineer Manufacturing/Process Engineer Controls Engineer Designer/Drafter Operations (Plant Engineering) Explore additional Engineering roles and learn more about how we support Engineering professionals: https://www.partnersinstaffing.com/find-jobs or https://www.partnersinstaffing.com/manufacturing-engineering Not the right fit

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