Not specified (assumed office-based unless stated otherwise).
7+ years project management experience
3+ years medical products industry
Direct supervision of project managers
The Integer Group is seeking a Manager of Program Management with a strong background in project management and leadership within the medical products industry. The ideal candidate will have at least seven years of experience, including supervision, and will be responsible for overseeing multiple projects, ensuring adherence to quality and regulatory standards, and fostering team development
Job Summary
The role requires leading direct reports including project and program managers while fostering their career development.
Candidates must ensure all assigned projects adhere to FDA regulations, quality management systems, and financial standards.
The position involves managing end-to-end execution of multiple complex projects from inception through successful implementation.
Matching Summary
Match Score: 85
The Integer Group is seeking a Manager of Program Management with a strong background in project management and leadership within the medical products industry. The ideal candidate will have at least seven years of experience, including supervision, and will be responsible for overseeing multiple projects, ensuring adherence to quality and regulatory standards, and fostering team development.
Skills & Requirements
Must-have
7+ years project management experience
3+ years medical products industry
Direct supervision of project managers
Oracle ERP system proficiency
FDA and ISO regulatory knowledge
Budget and revenue recognition management
Nice-to-have
Master's degree in business or technical field
Project/Program Management certification
Strong coaching and mentoring abilities
Experience with Product Development Process
Cross-functional collaboration skills
Key Requirements
Bachelor's degree in Engineering or related technical field
Minimum 7 years of total experience
Minimum 3 years in medical products industry
1-3 years of direct supervision experience preferred
Knowledge of FDA, ISO, MDD regulatory requirements