Director PMO Position Available In Rockingham, New Hampshire

Director PMO
R D Portsmouth, NH
We believe that great healthcare is an essential safeguard of human dignity.
At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you.
We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.

Who We’re Looking For:

As a key member of the R D team, the PMO Director will be responsible for leading the Project Management Office (PMO) for the Research & Development department. This role is crucial for overseeing the New Product Development (NPD) Review Board across all business units, driving strategic project planning, and executing medical device projects effectively. The PMO Director will manage a team of project managers, handle resource forecasting and capacity management, and ensure rigorous control over project portfolios.
About the

Role:

Chair and govern the NPD Review Board for all business units (Urology UR, Gastrointestinal GI, Obstetrics OB, and Interventional Urology IU).
Lead the development and execution of the R D annual operating plan specific to medical devices.
Drive and oversee resource forecasting, leveling, and capacity management for functions supporting R D projects, with a focus on medical device development.
Publish and maintain portfolio dashboards to provide visibility into project status, progress, and performance with a focus on medical device innovation.

Minimum Qualifications:

Bachelor’s degree in engineering, life sciences, or a related field. Minimum of 10 years of experience in project management within the medical device industry, with a strong background in R D.
Proven experience in leading cross-functional teams and managing complex medical device projects.
In-depth knowledge of medical device development processes, including design controls, risk management, and regulatory requirements (e.g., FDA, ISO 13485).

Preferred Qualifications:

Master’s degree or MBA preferred.
PMP Certification

Why Laborie:

Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.
Paid time off and paid volunteer time
Medical, Dental, Vision and Flexible Spending Account
Health Savings Account with Company Funded Contributions
401k Retirement Plan with Company Match
Parental Leave and Adoption Services
Health and Wellness Programs and Events
Awarded 2023 Cigna Healthy Workforce Designation Gold Level
Laborie provides equal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation, or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities.