About the Company Operating as a major global pharmaceutical organisation, our client is well known for its growth and innovation and is an Australian iconic brand in the marketplace. An opportunity has now arisen for a Validation Engineer to be responsible for planning, developing & executing qualification & commissioning activities for facility design, equipment & processes. About the Opportunity Reporting to the Site Manager, key duties include the following: Plan, coordinate & execute validation activities in accordance with the Site Validation Plans. Review cleanroom & HVAC design requirements in relation to GMP facility qualification. Develop & execute Qualification Protocols such as DQ, IQ, OQ & PQ. Contribute to GMP Facility Design Reviews & technical queries. Prepare & review validation reports aligned with Validation Strategies. Effectively liaise with internal & external key stakeholders. About You The successful candidate will have the following skills & experience: Tertiary qualifications in Engineering or Science. Sound industry experience in the pharmaceutical/life science or medical device industry. Minimum 5 years in validation & GMP facility qualification. Industry knowledge of cleanroom & HVAC design & qualifications. Sound time management skills & ability to multi-task. Well Developed interpersonal and communication skills. Ability to work with wide range of stakeholders. Culture & Benefits This is an Excellent Contract Opportunity for a talented Validation Engineer to be involved in a wide range of facility validation activities within the pharmaceutical industry involving qualification & commissioning. This role requires IMMEDIATE START. 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 for further information. NB - Only Shortlisted candidates will be contacted.
