About the Company Our client is one of the world’s leading global pharmaceutical manufacturers and suppliers of pharmaceutical related products for the local and export overseas market. Due to new project requirements, our client is now seeking a QC Instrument Validation Associate to be responsible for instrumentation qualification and data analysis of laboratory computer based equipment. About the Role Reporting to the QC Manager, key accountabilities include the following: Write and execute instrument qualifications including data integrity. Review & prepare qualification documentation & execution of documents. Perform testing to ensure systems are working as intended - lab equipment such as UVV, GC. plate reader & particle counters etc. Update SOPs, validation protocols & technical documents in relation to qualification and lifecycle management. Effectively liaise with internal & external key stakeholders in relation to computerised laboratory equipment. About you You will be a self-starter with the following skills and experience:



Tertiary qualifications in Science, IT or Computer Systems. Minimum 2 years of experience. Sound experience with instrument qualification of lab equipment. Industry experience in pharmaceutical/biotech industry. Experience in compliance with cGMP, GLP, GxP and Laboratory quality systems & requirements. Knowledge and understanding of GMP regulations. How To Apply This is an Excellent Contract Opportunity for a QC Instrument Validation Associate with sound laboratory instrumentation background to join a global pharmaceutical organisation to further develop their skills and experience within a highly regulated environment. This Chance is Long Term and requires Immediate Start. To apply for this role, please click the APPLY NOW button. For a confidential discussion please call Sue Campbell on 1300 793 994. PLEASE SUBMIT MS WORD DOCUMENTS ONLY

📌 Qc instrument validation associate (Australia)
🏢 Bell People Consultants
📍 Australia