About the Organisation Operating as a global pharmaceutical manufacturing organisation with world class manufacturing facilities, our client is known for its innovation, premium quality products and strong brand reputation. An opportunity has now arisen for a QA Associate with qualification & QA validation experience to support manufacturing with qualification activities and quality assurance. About the Opportunity Reporting to the Senior Manager, key responsibilities include: Perform routine quality walkthroughs of site GMP facilities & operations. Attend daily meetings to represent Quality at operational meetings. Review & approve QA validation & qualification documentation. Review all documentation in terms of compliance & regulation. Support revision & implementation of SOP's, protocols & other GMP documentation. Effectively liaise with key internal stakeholders. About You Tertiary qualifications in Science or related discipline. 3 to 5 years in pharmaceutical, medical device industries. Sound QA validation experience to support qualification activities. Sound GMP and manufacturing experience. Knowledge of TGA, FDA requirements. ERP & QMC systems. Sound communication & interpersonal skills. Ability to work independently & within a team. Culture & Opportunities This is an Excellent Opportunity for a QA Associate with validation experience to join a global organisation & support qualification activities in manufacturing. How To Apply To apply for this role, please click the APPLY NOW button. For confidential discussion, please contact Sue Campbell on 0417 994 917 or Maria Julienne on 0491 694 371. NB - Only shortlisted candidates will be contacted.
