Regulatory Program Manager

ManpowerGroup Global, Inc.

Maple Grove (MN)

Hybrid

USD 70,000 - 95,000

Full time

14 days+

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Job summary

Our client in the medical device industry seeks a Sr. Program Manager to join the Regulatory Program Management team. You will lead cross-functional initiatives and build comprehensive plans, budgets, and milestones.

Hybrid role in Maple Grove, MN (3 days onsite). Requires 5+ years of program management experience, a BS degree, and strong leadership and communication.

Qualifications

  • Minimum 5 years in a related program management role.
  • Bachelor of Science degree or equivalent professional experience.
  • Proven ability to manage large, complex projects across multiple teams and locations.

Responsibilities

  • Lead large-scale regulatory programs spanning multiple functional areas within the medical device sector.
  • Develop, prioritize, and submit comprehensive project plans, budgets, and methodologies for key initiatives.
  • Define project resources, establish milestones, and lead teams to achieve project goals effectively.
  • Take ownership of project implementation, ensuring alignment with organizational standards and objectives.
  • Support and motivate local Program Managers to manage scope, budgets, and timelines, fostering best practices and consistency across teams.

Skills

Program management
Leadership
Communication
Cross-functional collaboration
Regulatory/medical device knowledge

Education

Bachelor's Degree

Job description

Our client, a leader in the medical device industry, is seeking a Sr. Program Manager to join their team. As a Sr. Program Manager, you will be part of the Regulatory Program Management team supporting cross-functional initiatives. The ideal candidate will demonstrate strong leadership, strategic thinking, and excellent communication skills, which will align successfully in the organization.

Job Title:Sr. Program Manager

Location: Hybrid role atMaple Grove, MN (3 days onsite per week)

Pay Range:$60/hr w2

What's the Job?

  • Lead large-scale regulatory programs spanning multiple functional areas within the medical device sector.
  • Develop, prioritize, and submit comprehensive project plans, budgets, and methodologies for key initiatives.
  • Define project resources, establish milestones, and lead teams to achieve project goals effectively.
  • Take ownership of project implementation, ensuring alignment with organizational standards and objectives.
  • Support and motivate local Program Managers to manage scope, budgets, and timelines, fostering best practices and consistency across teams.

What's Needed?

  • Background with program and project management experience, with a minimum of 5 years in a related role.
  • Bachelor of Science degree or equivalent professional experience.
  • Proven ability to manage large, complex projects across multiple teams and locations.
  • Excellent communication, leadership, and organizational skills.
  • Experience supporting regulatory or medical device programs is preferred.

What's in it for me?

  • Opportunity to lead impactful projects in a dynamic industry.
  • Collaborate with diverse and talented teams across the organization.
  • Develop your leadership skills in a supportive environment.
  • Work onsite in Maple Grove, MN, with a focus on professional growth.
  • Be part of a company committed to innovation and excellence in healthcare.
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