Maureen Prosser

Maureen has over 30 years’ experience working in the pharmaceutical industry. Her Quality experience is within sterile and non-sterile manufacturing and commercial QA. She has an in-depth knowledge of quality and regulatory compliance, including cGMP, GLP, GCP, ICH, ISO, and Good Distribution Practice.

Maureen’s skills also include expertise in documentation preparation and management, ISO and GxP auditing including support for regulatory inspections, supplier qualification, and risk assessment and mitigation. She also has extensive experience in Release for Supply for the Australian and New Zealand market, clinical trial product manufacture, and implementation and management of quality systems.

With excellent attention to detail and a strong work ethic, Maureen can perform well in both highly independent and collaborative team environments.