Production and Project Lead for liquid and cream manufacturing facilities. - Manage Production requirements and resources for budget and growth.- Provide regulatory support to ensure compliance to required standards, TGA and ISO.- Support business growth activities and ESG.

• Manage regulatory requirements for the registration of medical device products, achieving listing on the Australian Register for Therapeutic Goods. • Establish relationships and liaise with government and industry stakeholders for the procurement of Covid Rapid Antigen Tests • Establish company procedures and requirements to meet supplier requirements of ISO13485 • Jointly with Managing Director develop the business strategy for the introduction of new medical device product to the APAC market and identify probable Australian manufacturing site

Lead and develop a team for the successful attainment of a TGA license to manufacture non-sterile therapeutic drug and sterile compounded product.* Commission and qualify a manufacturing facility to support the TGA manufacturing license* Fortify internal and external resources, in a 'Start-up' environment to meet changing demands* Develop partnerships with industry leaders and dynamic SME's for mutual growth* Liase and supply overseas market for Clinical Trial Products

Led product development and implementation for a national clinical trial which has now expanded globally.

Sydney based SME, designing and manufacturing architectural bespoke glass.ResponsibilityManage Financial accounts and all Capital Expenditure requirements for business growth and developmentLead Marketing Strategy including management of external suppliers and the Design, Development and Maintenance of WebsiteRationalise product offerings and pricing to meet a competitive market proposing substitute productsLead Sales strategies including the management of a contract Sales TeamComplete Design and Production activities to ensure on time product delivery and qualityManage growth with respect to; supplier management , customer agreements and promotion of industry standards

Enterix Australia provides an IVD in the form of Immunochemical FOBT provided through the Local GP or Pharmacy. Enterix was one of two FOBT’s selected for the Australian Pilot Bowel Cancer Screening program.ResponsibilitiesResource, Educate and Monitor effectiveness of Sales TeamDevelop and rollout an education program to General Practitioners and Pharmacy Identify and Implement Product and System improvements understood from the Pilot Program to support a National Rollout (NBCSP), in 2007.Coordinate screening initiatives with Key Stakeholders and Organisations.

Enterix Australia developed and manufactures the Immunochemical FOBT, offering the ‘home’ kit tests through the GP and Pharmacy. The test sample is returned to the laboratory and analysed using a recognition vision system integrated in an automated process.Responsible:Resources, training and processes for Laboratory and Manufacturing Area. Establish GMP and procedures for the laboratory, assembly area and warehouseConduct Batch Test Result / ReleaseSupply ManagementConduct GMP Audits of key suppliers (U.S. and Australia) for critical product componentryProjects:Identify and make ready a suitable new manufacturing site and coordinate the relocationSet up Laboratory and complete training in UK for Government Pilot Screening Trial

Maintain TGA license for Caringbah facilityManage the Quality Department, of 64 personnel responsible for; QC Chemical and Microbiological testing and release, Compliance Management, Validation and Change Control and Document Control.