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Engineering Project Management Director
2 months ago
About the Role
We are seeking a highly skilled and experienced Head of Engineering Project Management to join our team at Blatchford. As a key member of our R&D department, you will be responsible for leading our cross-functional engineering project teams and driving the execution of technical deliverables.
Key Responsibilities
- Develop and Deliver the R&D Product Development Roadmap: Create a comprehensive roadmap for product development, focusing on business goals and objectives.
- Support Commercial and Clinical Requirements: Collaborate with stakeholders to ensure commercial and clinical requirements are integrated into our innovation roadmap.
- Facilitate Project Definition and Documentation: Develop and document project scope, objectives, and desired business outcomes.
- Manage Stakeholder Expectations: Establish and manage stakeholder expectations, both internally and externally, through the use of EPM dashboards.
- Collaborate with R&D Leadership: Work with the R&D leadership team to prepare project budgets, ensure scope is realistic and accurate, and establish control to ensure fiscal and commercial compliance.
- Recruit, Develop, and Coach the Engineering Project Management Team: Lead a team of professional project managers, providing guidance, support, and development opportunities.
- Define and Report on Project Metrics and KPIs: Establish and report on measures and KPIs for all product development projects, ensuring business contributions are well-controlled.
- Manage Project Risk: Identify and mitigate project risks, particularly at system integration points, and propose timeline and budget plans to executive leadership.
- Collaborate with Senior R&D Functional Leaders: Work with senior R&D functional leaders to develop and execute corrective actions, addressing time pressures, skillset issues, or capacity opportunities.
- Manage Project Resourcing: Control and track project resourcing levels, including internal and external people resources, purchased materials, and device validation builds.
- Monitor and Coordinate Technical Documentation: Oversee and guide the creation of technical documentation across the Stage Gate process, ensuring compliance with ISO 13485, FDA, and MDR requirements.
What We Offer
- Competitive Salary
- 25 Days Holiday (Rising with Service)
- Option to Purchase Additional Annual Leave
- Flexible Hybrid Working
- Pension
- Death in Service
- Discounted Shopping and Leisure Activities
- Health Cash Plan
- Cycle to Work Scheme
Requirements
- BSc or Equivalent in Engineering
- Extensive Experience in Medical Device Development
- Demonstrated Experience of Direct Management and Leadership
- Ability to Work in a Fast-Paced Environment
- Solution-Oriented and Results-Driven
- High Level of Enthusiasm, Motivation, and Drive for Results
