Senior Project Manager

About the role

We are seeking a highly organised and collaborative Senior Project Manager to serve as the critical interface between our Peripheral Intervention Business Unit Leadership and cross functional teams in our medical devices organisation.

Role responsibilities include ensuring alignment between strategic objectives and project execution, driving visibility, coordination, and successful delivery of initiatives across R&D, Quality, Regulatory, Manufacturing, and Commercial functions.

Responsibilities

• Serve as the primary point of contact between the Business Unit and cross functional teams, ensuring effective communication and alignment.
• Coordinate and support projects throughout the product lifecycle, from concept development to commercialisation.
• Develop, maintain, and monitor project plans, schedules, milestones, and deliverables to ensure timely execution.
• Facilitate project governance activities, including status reviews, leadership updates, and portfolio planning meetings.
• Identify, track, and communicate project risks, dependencies, and issues, driving timely resolution and escalation when required.
• Collaborate with Engineering, Quality, Regulatory Affairs, Operations, Supply Chain, and other stakeholders to achieve project objectives.
• Ensure compliance with internal processes, design controls, and applicable regulatory requirements, including FDA and ISO 13485 standards.
• Support portfolio management activities such as project prioritisation, resource planning, and capacity management.
• Translate business strategies and objectives into actionable project plans that support commercial, clinical, and regulatory goals.
• Drive continuous improvement of project management, tracking, reporting, and cross functional collaboration processes.

Qualifications

• Bachelor's degree in Engineering, Life Sciences, Business, or related field.
• 8+ years of experience in project coordination, program management, or a similar role within medical devices (or highly regulated industry).
• Strong understanding of product development processes and regulatory environment.
• Excellent communication, organisational, and stakeholder management skills.
• Proven ability to manage multiple priorities in a fast paced environment.
• Preferred experience working with cross functional global teams.
• Knowledge of FDA regulations, ISO 13485, and design control processes.
• Familiarity with project management tools (e.g., MS Project, Jira, Smartsheet).
• PMP, PRINCE2, or equivalent certification.
• Experience supporting portfolio or program level initiatives.

Salary and Benefits

The Salary Range for this role is €100K - €120K + Bonus + Benefits.

Equal Opportunity Employer

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.