GILERO

Senior Project Manager - Medical Devices

GILERO Durham, North Carolina, United States

Medical Equipment Manufacturing · 51-200 employees

7 h ago
project-manager Principal (10+ yrs) Full-time United States
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About the role

The Senior Project Manager will lead complex medical and drug delivery device development projects from concept to commercialization while managing budgets, timelines, and engineering resources. They will also act as a mentor to junior staff, facilitate project meetings, and maintain strong relationships with clients and vendors.

What they look for

Project management Medical devices Drug delivery devices Engineering Client relations Budget management Timeline management FDA regulations ISO regulations Technical writing Data analysis Team leadership Vendor coordination QMS compliance Mentoring Project reporting

Requirements

Candidates must possess a Bachelor's degree in Engineering and at least 8 years of experience, with a minimum of 5 years specifically in medical device project management. Proficiency in FDA/ISO regulations and the ability to work on-site in Durham, NC at least 4 days a week are required.

Benefits

Annual bonus plan Medical insurance Dental insurance Vision insurance Life insurance Short-term disability Long-term disability 401(k) with match LinkedIn learning access

Full description

Are you an experienced Project Manager with a passion for bringing innovative medical and drug delivery devices to life? At Gilero’s Durham's office, we’re looking for a Senior Project Manager to lead design and development projects in cutting-edge healthcare solutions. In this role, you’ll drive complex projects from concept to commercialization, ensuring they stay on track, on budget, and meet the highest quality standards.

If you thrive in a fast-paced, collaborative environment where your expertise in project management, engineering, and client relations makes a real impact, this is the opportunity for you. Join us and be part of a company that values innovation, integrity, and excellence — while offering outstanding career development and growth potential.

Responsibilities:

  • Organize project activities, lead the project team, prioritize and delegate tasks to team members in adherence with timelines and budget requirements.
  • Lead multi-year medical and drug delivery development projects consisting of electronic as well as disposable devices.
  • Ensure project scope is maintained and/or manage out-of-scope requests.
  • Forecast engineering resources for short/mid/long-term project needs.
  • Generate financial and project reports for internal and external communication.
  • Liaise with the client for routine project updates, build relationships with clients.
  • Support Business Development through project timeline and budget preparation for new opportunities as well as project extensions.
  • Facilitate internal and external project meetings.
  • Grasp technical details with an ability to assist the team in decision-making.
  • Manage ongoing project timelines and budgets.
  • Maintain documents relating to the overall project (project plan, user needs, etc.). Ensure deliverables are being met and the customer is satisfied.
  • Coordinate vendor activities (suppliers, third-party labs, manufacturers, etc).
  • Ensure team members comply with established QMS guidelines/procedures/work instructions.
  • Act as a project coach for more junior project managers. Advise on projects. Mentor junior team members and engineering interns.
  • Support company-wide project management objectives.
  • Support the recruiting process by participating in interviews for the project management team.

Requirements:

  • BS in Engineering or 4-year technical degree.
  • PMP Certification (preferred).
  • Must be willing to work in the Durham office a minimum of 4 days a week.
  • 8+ years of experience with 5+ years of experience as a Project Manager in Medical Devices.
  • Knowledge of medical device regulations (FDA/ISO).
  • Possess strong project management skills and can work alone or in teams.
  • Strong writing skills and/or data analysis.
  • Ability to communicate effectively with customers and vendors in a technical capacity.
  • Competent computer skills, including Excel and Word.

Personal Attributes:

  • Meets Gilero Core Values: Collaboration, Integrity, Innovation, Excellence.
  • Comfortable and productive in a fast-paced, entrepreneurial environment.
  • A self-starter seeking a career opportunity with potential for internal advancement, seeking responsibility for core activities, and providing high-quality service to internal and external clients.
  • Commitment to excellence and quality service to external and internal customers.
  • Commitment to established policies and procedures, while contributing to continuous improvements.

Eligibility To Work:

  • Applicants must be permanently authorized to work in the United States without the need for employer sponsorship now or in the future.
  • Gilero does not offer sponsorship for employment authorizations (work visas).
  • We are an E-Verify employer and confirm work authorization for all new hires.

Why work at Gilero?

Founded in 2002, Gilero, a Sanner Group company, is an international contract engineering firm that specializes in the design, development, and manufacturing of novel medical devices and drug delivery products. At Gilero, we are proud of the culture we have built that directly reflects our values of excellence, integrity, innovation, and collaboration. Motivated by our purpose to benefit people and improve patient outcomes, our team continues to grow at a rapid pace. US locations include Carlsbad, CA; Chicago, IL; as well as NC locations in Raleigh, Durham, Greensboro, and Pittsboro.

You will enjoy an annual bonus plan, Medical (3 BCBS plans to choose from), dental and vision, company-provided life insurance, short-term and long-term disability, 401(k) with a match the first month you start with a zero-vesting period, and access to LinkedIn learning for personal and professional development.

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