Bringing together teams of subject matter experts and leaders to collaborate and improve operational excellence for inbound supply chain. Refining mission statements, identifying opportunities to deal with current issues, building future-focused approaches to address supply chain complexity, resilience, waste and sustainability.Leading strategic initiatives, managing complex challenges, and facilitating high-impact meetings by enthusing, guiding and challenging teams to deliver value and achieve operational excellence focused on transforming the inbound supply chain for the benefit of the entire Biopharma an MedTech industry.

Identified opportunities to reduce cost on standard of care programmes. Supported Operational Excellence Improvements across Global Pharmaceutical Development, advised on best practices for Procurement / Vendor Management, evaluated statements of work, trained on budgets, accruals and invoices.

Led a department responsible for planning, co-ordination and distribution of programmes for Clinical Trial Supply. Provided technical and personnel management of multi-disciplinary teams within Pharm Dev, including development, coaching, appraising, budgeting, KPI oversight and leading Process Improvements. Responsible overall adherence to FDA, DEA, MHRA, GXP and GMP requirements.

Managed a team responsible for planning and co-ordination of materials for Clinical Trial Supply. Provided general line management responsibilities, including development, coaching and appraising for a multi-disciplined team while running Continuous Improvements projects.

Coordination and supply of investigational medicinal products (IMP) to and from study sites for use in clinical trial studies. Preparation of study specifications and IMP schedule / forecast management ensuing timelines were met while supporting Continuous Improvement programs.

Project Management of growth focused, range extensions, quality improvement and value-added projects. Drove results through detailed project planning, managed small internal teams including Engineers, Marketing, Regulatory and QA. Ensured projects adhere to registration, regulatory and quality requirements.

Worked with engineers, marketing and registration to provide project support, generated biocompatibility reports required for audit adhering to registration, regulatory and quality requirements.