About the Company Operating as a global pharmaceutical player, our client is well known for its growth and innovation offering a range of healthcare and pharmaceutical products to local & global markets. An Opportunity has now arisen for a QA Associate to work closely with manufacturing operations for document review, change controls, CAPA's and validation operations. About the Opportunity Reporting to the Quality Manager, key duties include the following: Perform routine quality walkthroughs of the GMP facility operations. Provide support, review & approval of GMP documentation. Review quality documents, change control, CAPA's & quality compliance work. Review validation protocols. document review & validation. Engage with manufacturing to for quality problem solving.( Collaborate with cross functional teams & effectively liaise with all parties. About You The successful candidate will have the following skills & experience: Tertiary qualifications in Science or Engineering. Sound experience in QA within a Pharmaceutical/Medical Device. Sound knowledge of QA, CAPA's & deviations and document review. Strong GMP knowledge. Excellent Attention to detail & strong organisational skills. Well developed interpersonal & communication skills. Ability to work with wide range of stakeholders. Culture & Benefits This is an Excellent Contract Opportunity for a QA Associate to join a leading global pharmaceutical organisation to support manufacturing operations, drive change controls & deviations for a major project. How To Apply To Apply for this role, please click the APPLY NOW button. For a confidential discussion, please contact Sue Campbell on 0417 994 917. NB - Only Shortlisted candidates will be contacted.
