Regulatory Affairs Program Manager
• Master’s degree and a minimum of 3+ years of Program Management experience including broad multi-functional business experience along with 3+ years of project and/or people management experience
• Program manager experience
• Experience managing global initiatives
• Experience driving change management initiatives across an organization
• Experience leading efforts in a regulated environment
• Experience with MS Project, MS Excel, MS PowerPoint and MS Word
• Self-motivated individual with passion to succeed
• Demonstrated leadership for business process harmonization across an organization
• Experience implementing initiatives through effective influence management skills at multiple levels in the organization
• Prior consulting experience
• Excellent verbal and written communication and presentation skills
• Experience in creating and delivering presentations to senior leadership
• Excellent facilitation and issue resolution skills
• Previous experience managing in a matrix organization
• Ability to work independently or collaboratively to determine and develop approaches to solutions with very little to no supervision or direction
• Experience in the medical industry, ideally the medical device or pharmaceutical industry
• General knowledge of Regulatory Affairs, Clinical, Quality Management Systems and compliance requirements for medical devices
• Experience providing work direction and leadership to people and teams in a management role
• Master’s degree in engineering, business or related field
• PMP Certification or other formal Project Management training and experience