Sarah Winwood

Responsible for managing the delivery of client facing gene editing projects, as well as several internal, cross-functional projects, including: • Capacity Increase Programme for Cell Line Engineering and Arrayed Screening • Diagnostic Reagents Pipeline Re-Design and Re-Development • Relocating Operations from Vienna, Austria to Cambridge, UK • Relocating Cryopreserved Inventory from Boston, USA, to Cambridge, UK • In Vivo Sales Order Process Streamlining and Optimisation in Philadelphia, USA • ERP (Microsoft Dynamics AX 2012) Systems Upgrade • Logistics Capability and Capacity Increase

Promoted to Team Leader of the Cell Line Products team, continuing responsibility for the delivery of high-quality cell line products under ISO 9001:2015 and ISO 13485: • Expanding the Product Delivery Options to Support Internal Teams • Implementing Automated Cell Culture Robotics into the Production Pipeline • Business Lead for ERP System (Microsoft Dynamics AX 2012) • Preparing Raw Data for Migration into Microsoft Dynamics AX 2012 • Performing User Acceptance Testing • Preparing Standard Operating Procedures (SOPs) • Training End Users

Coordinating the activities of the Cell Line Products team, responsible for the delivery of high-quality cell line products under ISO 9001:2015 and ISO 13485: • Delivering Training for Several Scientific Techniques e.g. Aseptic Technique, Sub-Culturing, Harvesting and Reagent Preparation • Overseeing Tasks Relating to Molecular Biology e.g. PCR and DNA Sequencing Analysis • Implementing a new Barcode System for Sample Tracking and Inventory Management • Applying for Relevant Import and Export Licences to Facilitate the Shipping of Products around the World

• Introducing a New Technical Support System • Providing Scientific Support by Phone and Email to Customers Requesting Product Guidance and/or Help Troubleshooting Experiments • Supporting Local and International Field-Based Teams by Answering Scientific Inquiries • Assisting in the Preparation and Review of Technical Documents and Web Content for New and Existing Products • Key Member of the Team Implementing ISO9001 • Developing and Implementing a CAPA System • Presenting Technical and Business Data • Business Lead for Company-Wide Transition from Excel to SQL Database

• Performing Mammalian Cell Culture (Adherent and Suspension) • Carrying Out Experiments, Data Collection and Analysis • Establishing Laboratory Standard Operating Procedures (SOPs) • Developing and Batch Manufacturing Record (BMR) Templates • Curating and Maintaining the Inventory Management System

• Testing Finished Product under GMP and to ISO 9001 Compliance • Completing Batch Manufacturing Records (BMRs) Documentation • Performing Out-of-Specification and Out-of-Tolerance Investigations

Product Development Project – Creation of a new Tricalcium Phosphate Granule • Planning and Carrying Out Process Trials • Optimising the Manufacturing Process • Final Year Thesis – Awarded Grade A1 • Manufacturing and Testing Final Product