Senior Project Manager (Northfield)
Medline
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/dietary supplement/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).
$225k - $240k
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