Program Manager, Labeling Development

Medtronic   •  

Fridley, MN

Industry: Manufacturing

  •  

5 - 7 years

Posted 104 days ago

This job is no longer available.

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The Restorative Therapies Group develops life-restoring therapies and healthcare solutions that span the care continuum; integrating technologies and applying clinical and economic evidence to increase patient access, improve efficiency of procedures and deliver successful patient outcomes
As a Program Manager in this role, you will be responsible for managing program initiatives and/or program teams in support of RTG (Pain and Pelvic Health) Labeling.

Day in Life-


• Partner with a wide variety of functional areas to gather information required to maintain, update existing labeling, and track approved labeling and indications globally• Manage complex labeling-related programs, schedules, milestones, inter-dependencies, deliverables, and resources.• Oversee program teams and activities to meet business plan and quality requirements• Act as a focal point for and liaison to functional and program managers for planning, development, logistics, quality, etc.• Work with management and functional groups to ensure use of standard business processes and procedures to support compliance with federal and international regulations and industry standards. • Identify and/or participate in strategic cross-team or cross-functional initiatives and opportunities when appropriate. • Partner with wide variety of functional areas to gather information required to write accurate user instructions.• Work cross-team and cross-functionally to plan, budget, coordinate and manage programs, milestones, program priorities, and resources • Participate, or ensure team participation on, high-level product development team(s) as appropriate.• Coordinate/manage program team work with all related functional groups and outside contractors and suppliers • Serve as key communications contact with management to provide information on schedules, milestones, deliverables, etc., and to identify resource issues and needs• Ensure personal understanding of all quality policy/system items that are personally applicable.• Follow all work/quality procedures to ensure quality system compliance and high quality work.

Must Have:

Minimum Qualifications• BA/BS degree with 5+ years of relevant program management experience; or a MA/MS with 3+ years of relevant program management experience
Nice to Have• 5+ years of job-related experience in a labeling creation environment or medical device industry• Experience leading business programs to completion• Demonstrated excellent people and communication skills (verbal and written)• Demonstrated strong organizational skills• Experience managing multiple programs successfully• Experience using electronic tools for managing programs, routing reviews and approvals, allocating resources, etc.• Proven ability to interact with a broad range of functional groups and individuals at various levels of the organization• Experience managing complex programs, especially electronic products, labeling, and/or medical devices• Experience in program resource coordination• 5+ years of experience in cross-functional, cross-geography program management• Experience working in a regulated environment• Experience working in an international organization• Management/supervisory experience• Experience working with cross-geography programs and teams• Experience working on programs requiring localization/translation

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