Senior Project Manager

7 days ago


Basingstoke, Hampshire, United Kingdom Blatchford Full time

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 incorporated 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


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