Senior Medical Device Program Manager

Medline Industries, LP; United States; On-site; USD 92,000 - 138,000; Full time

Job summary

Medline Industries, LP is seeking a Senior Project Manager to guide the development of medical devices, dietary supplements, cosmetics, and OTC drugs. You will lead cross-functional teams across R&D, quality, regulatory, manufacturing, and product divisions to deliver on strategic initiatives.

The role emphasizes portfolio management, planning, budgeting, and keeping projects on schedule, with a focus on design controls, risk assessments, and the 510(k) process. Travel up to 10% may be required.

Qualifications

• Education: Bachelor's degree in Engineering or Science related field.
• Certification: PMP Certification.
• Experience: At least 4 years in a medical device, pharmaceutical, dietary supplement or cosmetic related field.
• Experience: At least 2 years of project management experience.
• Experience with development and launch of new medical/pharma/dietary supplement/cosmetic products.
• Knowledge of medical device requirements (Class I-II), design controls, risk assessments, and the 510k process.
• Travel up to 10% of the time (domestic and international).

Responsibilities

• Guide the development of medical devices, dietary supplements, cosmetics, and OTC drugs.
• Lead cross-functional teams across R&D, quality, regulatory, manufacturing, and product divisions.
• Manage project plans, budgets, scope, timelines, and projected end dates.
• Develop risk assessments and contingency plans to mitigate delays or cost overruns.
• Ensure alignment with divisional strategies and milestones.
• Coach junior staff and provide status updates to leadership.

Skills

Project management

Agile methodologies

Risk assessments

Education

Bachelor's degree in Engineering or Science related field

PMP Certification

Job description

Medline Industries, LP is seeking a Senior Project Manager to guide the development of medical devices, dietary supplements, cosmetics, and OTC drugs. You will lead cross-functional teams across R&D, quality, regulatory, manufacturing, and product divisions to deliver on strategic initiatives.

The role emphasizes portfolio management, planning, budgeting, and keeping projects on schedule, with a focus on design controls, risk assessments, and the 510(k) process. Travel up to 10% may be required.