Regulatory Affairs Program Manager - Hybrid

Details for the position are as follows:

• 12-month contract to start with the possibility of extension or conversion depending on performance and business needs
• Rate: $57-67 an hour
• Location:
  
  Maple Grove, MN – Hybrid – 40 hours a week

• The program manager will be responsible for large scale regulatory program management, which spans many functional areas and aligns a process across the medical device businesses.
• Develop, prioritize and submit project plans, budgets and methodologies across a range of key projects. Define project resources, milestones, and lead teams to execute goals. Take ownership of the successful implementation of a set of projects that collectively can comprise a program.
• Support/motivate the local Program Managers to manage the total scope of the required changes necessary to bring their processes up to standards. Support/motivate the local Program Managers to manage the budget and timetable for the implementation of processes in conjunction with our corporate PMO team. Establish teams from all locations/businesses to share best practice and ensure consistency. Provide regular communications of project status to Division staff.
  
  Provide training and implementation planning support to all program participants. Plan to evaluate external consultants to optimize costs and benefits.
• This position is non-exempt with no direct reports

• Bachelor’s degree required, Master’s degree preferred
• 5+ years of Project/Program Management experience -- Leading complex and/or critical programs within the Global Regulatory Services organization, including Extended Producer Responsibility (EPR) initiatives being ideal.
• Medical device industry experience required
• Strong Project management experience within Regulatory affairs required

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