Regulatory Program Manager

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

About the role

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.

Requirements

• 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

Benefits

• 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

Pay

$60/hr W2