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Medical Device Product Development Manager Jobs in Raleigh, NC

Manager, Product Development

Cary, NC

$107K - $133K/yr

Manager, Product Development: Atticus LLC About Us Atticus is a demand-driven manufacturer of ... Comprehensive medical, dental, and vision benefits beginning Day 1 * Company performancebased ...

Manager, Product Development

Cary, NC · On-site

$107K - $133K/yr

Manager, Product Development: Atticus LLC About Us Atticus is a demand-driven manufacturer of ... Comprehensive medical, dental, and vision benefits beginning Day 1 * Company performancebased ...

Our history includes the development of many innovative medicines, notably the discovery of the ... This role ensures that medical device complaints are consistently captured, appropriately triaged ...

Our history includes the development of many innovative medicines, notably the discovery of the ... This role ensures that medical device complaints are consistently captured, appropriately triaged ...

Senior Device Quality Engineer

Zebulon, NC · On-site

$75K - $101K/yr

... development to post-market surveillance for ... medical devices within combination products. Responsibilities include risk management ...

This position reports to the Regional Sales Manager and is part of the Blood Gas Sales Team and ... in a medical device industry preferred * 1+ years capital equipment sales experience preferred ...

Sales Representative Medical Device

Raleigh, NC · On-site +1

$90K - $100K/yr

This position reports to the Regional Sales Manager and is part of the Blood Gas Sales Team and ... in a medical device industry preferred * 1+ years capital equipment sales experience preferred ...

Lead development teams by maintaining strong technical understanding of systems, promoting sound engineering practices, and ensuring high-quality delivery. * Identify, assess, and manage product and ...

Project Manager, R&D

Raleigh, NC · On-site

$120K - $165K/yr

As a Program Manager within our Connected Care R&D organization , your contributions directly ... Oversee the endtoend lifecycle of a software medical device product from discovery through ...

Sr. R&D Engineer, New Products

Raleigh, NC · On-site

$101K - $139K/yr

In this role, you will partner closely with cross-functional teams across R&D, Product Management ... end-use product applications * Experience in the medical device industry Pay Transparency If ...

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Showing results 1-20

Medical Device Product Development Manager information

See Raleigh, NC salary details

$41.3K

$123.4K

$140.5K

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

As of Jun 14, 2026, the average yearly pay for medical device product development manager in Raleigh, NC is $123,442.00, according to ZipRecruiter salary data. Most workers in this role earn between $111,300.00 and $139,000.00 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.
Manager, Product Development

Manager, Product Development

Capital Bank

Cary, NC

$107K - $133K/yr

Full-time

Medical, Dental, Vision

Posted 28 days ago


Job description

Manager, Product Development: Atticus LLC

About Us

Atticus is a demand-driven manufacturer of Battle-Tested Chemistries; 100% American-Owned with a purpose to Enhance Daily Life and committed to long-term viability. Through our Agriculture and EcoCore portfolios, we are committed to the protection of critical food supply and beautification of our environment. With 95%formulationon US soil and the broadest, most diversified portfolio in the industry, we aim to execute with clarity and focus - delivering on our value proposition: Relevant. Simple. Reliable. For more information and a complete list of products, visit AtticusLLC.com.

What you will do in this role

The Manager, Product Development will be responsible for owning formulation development projects for Atticus LLC. This role will work closely with our manufacturing, sourcing and development partners (both US and offshore). In this role you will manage formulation validation activities, ensure regulatory alignment and EPA Submission prep and oversee Technology Transfer and Scale Up. The Manager, Product Development will report to the Director, Development & Regulatory Alignment.

Responsibilities

Formulation Development:

  • Owns formulation development projects for certain market segments (US Domestic or with offshore manufacturing/sourcing/development partners)
  • Formulation Validation:
    • Work with Development Laboratories to ensure that the final product matches the reference product including tank mixes and custom blends for seed treatment products
    • Provide guidance to laboratories on formulation types, including CS formulations and blends of AI's with or on fertilizer.
    • Source reference samples for reverse engineering.
    • Maintain project details and timelines within Smartsheet for accurate tracking and communication with stakeholders.
  • Regulatory Alignment and EPA Submission Prep:
    • For new market Segments, prepare Development CSF and SDS' necessary for EPA registration.
    • Upon final formulation, arrange sample preparation for GLP, Tox, and Seed Safety studies and send samples to the appropriate locations.
    • Confirm inert ingredients are approved by EPA for use in pesticide formulations.
    • Provide inert guidance to development labs outside of USA on use of EPA approved ingredients during development process.
  • Technology Transfer and Scale-up:
    • Work with Operations to conduct and coordinate pilot production runs as needed.
    • Provide guidance and heads up to Procurement Lead when new inert ingredients are used in new products to allow early development of sourcing strategy.
    • Prepare initial Manufacturing Manual for all new products prior to pilot trials or first commercial campaign.
    • Prepare initial bulk BOM for all new products within ERP system to ensure proper usage factors and use of fully vetted alternate ingredients, as applicable.
    • Develop initial finished product specifications including analytical methods and physical testing procedures to include in the Manufacturing Manual.
    • Manage and facilitate post Pilot testing of samples at appropriate development lab and adjust Manufacturing Manual as appropriate.
  • Manage and facilitate sample shipment requests for internal and external customers
  • Support creation of Safety Data Sheets (SDS).
  • Supports commercialization of new products and change management of existing products.

Manufacturing Support and Additional items:

  • Work with Operations to maintain and approve Manufacturing Manuals, including procedures and product specifications.
  • Coordinate efforts with labs and Operations to resolve quality complaints.
  • Work with Operations and Procurement on cost reduction efforts and/or sourcing initiatives that lead to testing and approval of alternate ingredients. Manage testing of alternate ingredients with labs and coordinate CSF updates with Regulatory Team.
  • Support and coordinate formulation testing for trait technology listings (e.g., Enlist, XtendiMax, Engenia, etc.) as needed.

Required Skills/Qualifications

  • Bachelor's degree from a four-year college or university in business, supply chain management, technical discipline or equivalent focus required, advanced degree preferred.
  • Five to ten years related experience; or equivalent combination of education and experience, preferably in agriculture or chemical field.
  • Excellent interpersonal skills and proactive communication skills. Ability to network within the organization as well as with external parties.
  • Strong written, verbal, and presentation skills.
  • Exceeds customer quality and service expectations through attention to detail
  • Demonstrates leadership skills in driving change and improving the integrity of applicable processes and systems.
  • Ability to work effectively across diverse and cross-functional teams, under critical timelines and while balancing the needs of internal and external customers.
  • Intermediate level Microsoft Office skills.

Why Atticus?

Atticus is committed to the longterm success of our industry and our people. Through active involvement in key task forces and partnerships with organizations shaping tomorrow's leaders, we demonstrate responsible stewardship, promote safe product use, and advance the Agriculture and EcoCore markets we serve.

Through our employee experience,Atticus Freedom, we intentionally invest in our team by providing the tools, support, and environment needed to perform at a high level. Our culture is not a program - it is embedded in how we operate, collaborate, and make decisions. By prioritizing professional development, leadership growth, and overall health and wellbeing, we build a strong, unified team aligned by shared values - together asOne Atticus.


What We Offer Our SuCitta Warriors

Our people are our most valuable asset. Atticus offers a comprehensive and competitive total rewards package designed to support both professional success and personal wellbeing, including:

  • Comprehensive medical, dental, and vision benefits beginning Day 1
  • Company performancebased quarterly bonus opportunitiesthrough theSuCitta Warrior Achievement Plan (SWAP), allowing team members to share directly in the success of the company
  • Employee Stock Ownership Plan (SuCitta Stealth), providing longterm ownership and alignment with Atticus' growth
  • A thoughtfully designed workplace experiencethat supports physical, mental, and emotional wellbeing
  • Ongoing professional and leadership development opportunities
  • A valuesdriven culturegrounded in accountability, adaptability, decisiveness, and a commitment to delivering results


At Atticus, greatness is earned. We seek individuals who are driven by purpose, energized by challenge, and motivated to contribute to something bigger than themselves. If you thrive in a fastpaced environment and are committed to excellence, you will find a home here.

Get a glimpse of our team and culture by watching ourFort 940 Tour: Here

Join Atticus and become part of a team that values ownership, integrity, and the courage to escape the ordinary.


Atticus, LLC is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions of this position.

Atticus LLC participates in E-Verify.


Recruiting Agencies, Please Note:

Atticus, LLC will not accept unsolicited assistance from recruiting/search agencies for this employment opportunity. Please, no phone calls or emails. All resumes submitted by recruiting or search agencies to any employee at Atticus, LLC via email, the Internet or in any form and/or method without a valid written search/recruitment agreement in place for this position will be deemed the sole property of Atticus, LLC. No fee will be paid in the event the candidate is hired by Atticus, LLC as a result of the referral or through other means.