Greg White Email Address

Associate Director, Quality Engineering and Systems

Mayne Pharma is a fast growing company, focused on applying its drug delivery expertise to commercialize branded and generic pharmaceuticals, with operations in Australia and the US. The Company has grown substantially and reflects the hard work and dedication of its employees and their adherence to corporate values.

PROFESSIONAL EXPERIENCE: Mayne Pharma: Senior Quality Associate - Facilities: Responsible for QA Oversight of new manufacturing facility. Patheon: Manager of Automation and Facilities Validation July 2015 to November 2015. In October, I was contacted and offered the QA position above. Group Leader - Validation - March 2013 to Present: Manage work activities of Validation Associates in Automation Validation. Responsible for ensuring Steriles and Orals Solid Dosage Operations Automation change control and validation readiness in order to meet Production schedule. DSM Pharmaceuticals Inc, Principle Quality Associate – August 2007 to March 2013: In addition to responsibilities below, became more interactive in management of Quality and Validation systems (e.g. making critical decisions about production/revalidation processes and authoring procedures). Responsible for Manufacturing Quality Oversight of sterile drug processing. Liason between DSM and external customers. Senior Quality Associate – November 2003 to August 2007 Responsible for QA oversight for sterile products as well as oral and topical products computer, equipment, and lab validation. Cross trained in process validation. Mentor for QA and Validation employees (cross training) Perform SOP authorship, consensus, and review. Lead QA associate on multiple production line upgrades and installations. Validation Associate III – May 2003 to November 2003 Added review of cleaning and process validation documentation responsibilities. Validation Associate II – February 2002 to May 2003. Review and approval of validation documents, training users on Document Management System and Validation databases. Responsible for computer, equipment, and lab Validation. Team leader for validation contractor group. Participate in regulatory audits.