Project Manager overseeing project delivery for B2B Corporate Transformation at Talent Garden. Ensure high - quality execution and client relations in a hybrid learning context.
About the role
- Senior Project Manager leading complex R&D projects in medical device sector at Teleflex, focusing on cross-functional collaboration and project execution.
Responsibilities
- Lead end-to-end execution of complex, cross-functional and cross-BU R&D projects and programs.
- Build team ownership and commitment to project and business plans and define project milestones, deliverables, and associated resource requirements.
- Ensure alignment of R&D initiatives with business objectives and portfolio priorities.
- Actively build and foster collaborative relationships across all levels to improve overall outcomes and timely project/program execution.
- Support R&D portfolio planning, prioritization, and capacity management.
- Prepare and present project and portfolio status to senior leadership and governance boards.
- Own and manage the initiation, planning, executing, monitoring & controlling and closing of Tracheostomy Sustaining and NPD projects.
- Ensure overall compliance; promote creative solutions.
- Lead/coordinate project activities with Regulatory Affairs, Clinical Medical Affairs, and other shared service teams as required.
- Mentor and coach Project Managers and R&D team members, drive lessons learned and best-practice sharing across the entire team.
Requirements
- Bachelor’s degree in business or science discipline or equivalent education/experience required.
- 8-10 years of engineering and/or project management experience preferably in the Medical Device or other regulated industry.
- PMP or other formal Project Management Certification preferred.
- Proven track record managing complex, cross-functional R&D projects.
- Excellent stakeholder management, communication, and leadership skills and influence at all levels of the organization.
- Excellent verbal/written communication and presentation skills.
- Ability to support multiple projects and balance priorities, work independently or collaboratively to determine and develop solutions.
- Familiarity with ISO 13485, MDR, FDA 21 CFR Part 820 Design Control, ISO 14971, GMP and other standards as they relate to the development and manufacture of medical devices would be an advantage.
Benefits
- Health benefits
- Retirement plans
- Paid time off
- Flexible working arrangements
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
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