Senior Project Manager

Medline Northfield, IL Open
Medline is looking for Senior Project Manager in Northfield, IL.
This local job opportunity with ID 3892953367 is live since 2026-10-16 05:57:23.
Job Description

The position will guide the development of medical devices, dietary supplements, cosmetics, and/or OTC drugs. Lead collaborative, multifunctional teams consisting of R&D personnel, quality, regulatory, manufacturing, and product divisions. Will serve as a subject matter expert on all phases of product development and is responsible for managing and overseeing all aspects of a project portfolio spanning multiple priorities and functional areas.




MAJOR RESPONSIBILITIES:



  • Manage the product development process utilizing various project management frameworks such as iterative agile.

  • Manage project portfolios and ensure that project and divisional goals are aligned.

  • Provide updates to and advise divisional leadership on project status and opportunities.

  • Collaborate with product divisions to compile strategic plans, establish innovation pipelines, and align product development efforts with long-term divisional strategies.

  • Manage assigned projects, balance corporate priorities, and ensure team alignment across functional areas to ensure that project deadlines and goals are met.

  • Develop, communicate, and track project plans, objectives, budgets, scope, timelines, and projected end dates.

  • Translate project goals into project tasks.

  • Leader in the use and application Medline’s Project Management Portal to execute projects effectively.

  • Leverage lessons learned to conduct risk assessments and identify issues that may cause project delays or cost overruns.

  • Develop and implement contingency plans to mitigate the impact.

  • Compile risk profiles associated with scope creep and changing project requirements.

  • Maintain team morale and engagement by ensuring constant and transparent communication. Generate team consensus.

  • Lead project and process best practice guidance to cross-functions team members. Supervise, coach, and train junior staff.

  • Compile technical justifications and data summaries in support of product claims.

  • Lead process improvement initiatives or additional quality initiatives as project manager.

  • Keep current with regulatory guidelines, technical innovations, and new developments within the medical device or pharmaceutical industry.




MINIMUM JOB REQUIREMENTS:


Education:



  • Bachelor's degree in Engineering or Science related field.




Licensure/Certification:



  • PMP Certification




Work Experience:



  • At least 4 years of experience in a medical device, pharmaceutical, dietary supplement or cosmetic related field.

  • At least 2 years of project management experience.

  • Experience in the development and launch of new medical/pharma/dietarysupplement/cosmetic products.

  • Experience with medical device requirements (Class I-II), design controls, risk assessments, and the 510k process.




Knowledge / Skills / Abilities:



  • Project management tools and techniques.

  • Knowledge of medical device requirements (Class I-II), design controls, risk assessments, and the 510k process.

  • Position may require travel up to 10% of the time for business purposes (domestic and international).

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