Lead cross-functional teams in the delivery of injection products for diabetes care. Focus on R&D workstreams for major initiatives and product development programmes. Role centres around managing critical projects that support business continuity, innovation, and compliance.
Responsibilities:
- Lead and coordinate cross-functional R&D teams for key projects (compliance, cost savings, form/fit/function changes, and business opportunities).
- Act as liaison between leadership, functional managers, and project teams.
- Prioritise, resource, and track progress of projects within a portfolio.
- Report on program progress (quality, cost, schedule) to senior management.
- Ensure sufficient resource allocation and spending to meet deadlines.
- Support and maintain rigorous project planning across teams.
- Lead the implementation and use of a global portfolio management tool.
Qualifications:
- Bachelor's degree in engineering or scientific discipline.
- Minimum 5 years' experience managing Class II/III medical device projects.
- Experience in high-volume manufacturing and lifecycle management.
- Strong leadership, communication, and organisational skills.
- Proven track record in project planning, team management, and budgeting.
- Skilled in stakeholder influence and conflict resolution.
- Experience in product development processes, regulatory standards, ISO, GMP, and FDA requirements.
- Competent with tools like MS Project, Celoxis, Monday.com, etc.
- PMP or equivalent certification preferred.
