Lisa Wright Email & Phone Number

Adelaide, Sa, Au

Adelaide, South Australia, Australia

Adelaide, South Australia, Australia

 Manage Bickford’s New Product (Liquid Formulation) Development (NPD) function  Lead and execute site GMP compliance projects  Identify and drive continuous improvements initiatives in Good Manufacturing Practice (GMP) and Food Safety Culture Achievements  Complete refresh of NPD and regulatory documentation to improve facilitation of NPD processes and inter-departmental communications Identified a range of improvements for Bickford’s site Clean in Place (CIP) systems to ensure consistently compliant CIP’s  Compilation and oversight of a site CAPEX for wide ranging facility improvements as part of compliance improvements projects  Identification and purchase of new laboratory equipment (UV-Vis Spectrophotometer and Moisture Analyser) to expand and improve QC and NPD capabilities

Adelaide, South Australia, Australia

 Manage site GMP improvements projects Drive continuous improvement  Support Bickford’s Food Safety Culture initiatives  Oversee Bickford’s Product Stability program  Pro-active member of Bickford’s HACCP Team Achievements  Compiled and co-presented recommendation to the business on direction and plan for site TGA compliance  Developed and implemented a set of new GMP Training modules for staff (both Operational and non-Operational)  Co-developed and rolled out a new Food Safety Culture program  Lead implementation of SharePoint for Operations  Developed and implemented various new and / or significantly improved Quality Systems including Change Management, Internal Audits, and HACCP Plans

Australia

Development and implementation of TGA compliant Quality Systems and operations processes  Complete review and upgrade of Bickford’s Quality Management Systems to meet TGA standards and improve Food Safety compliance  Develop and roll out Quality Management Systems training packages to Operations employees at all levels  Participate in and support external certification audits Achievements  Review and implementation of improvements to allergens management, and cleaning and environmental monitoring processes to meet both TGA and Dairy Safe expectations  Drove GMP improvements to enable full Dairy Safe compliance and accreditation. From audit report: “The Bickford's team are to be commended on the effort and commitment demonstrated to deliver continuous improvement with systems, outputs and outcomes” in relation to the work I have been implementing

Mount Barker, South Australia, Australia

Mount Barker, South Australia, Australia

 Manage and maintain Jurlique’s TGA license compliance  Manage and maintain Jurlique’s ISO 9001:2015 and ISO 22716:2007 certification  Oversee Jurlique’s Quality Management Systems in accordance with cGMP  Ensure goods are released in accordance with Market Authorisation  Responsible for identifying and implementing Product Recall process with the TGA and / or ACCC  Vendor Assurance accountabilities including continuous improvement with vendors, GMP contractual agreements, and approval of new vendors Accountable for complaints reporting  Part of the Jurlique Operations Leadership Team Strategic planning Manage the Quality department budgetsAchievements  Approached to remain at Jurlique for an additional 5 weeks after initial redundancy date to undertake regulatory risk reviews  Gained both ISO 9001:2015 and ISO 22716:2007 within 3 months of making decision to obtain accreditation and without requiring a third-party consultant. Both certification audits resulted in zero non-conformances  Lead multiple external audits including TGA, ISO, and by Jurlique’s parent company, Pola Orbis Holdings  Project managed a detailed process review of Jurlique’s entire raw material handling practices from receipt to use in bulk manufacture to identify risks (including mix ups and contamination) after an issue resulted in a product recall  Project managed a full risk review of Jurlique’s artwork process to identify potential for errors to prevent future product recalls. Wrote technical instructions to clarify and improve the process

Mount Barker, South Australia, Australia

Management of Jurlique's Quality Control department activities and people, including vendor management, in accordance with GMP and GLP

Adelaide, South Australia, Australia

Management of laboratory and production of oligonucleotides (synthetic DNA).

Operation of DNA Synthesisers and customer service

Salisbury, South Australia, Australia

Quality Control testing of personal and health care products, includeing stability testing and raw materials used for manufacture