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 global market. Due to global expansion and growth, an opportunity has now arisen for a Validation Specialist to be responsible for validation protocols. About the Opportunity Reporting directly into the R&D Validation Manager, key responsibilities include: Review equipment validation activites, prepare & execute validation protocols. Review & prepare validation protocols for variety of equipment such as temperature Mapping, isolators, autoclaves, integrity testing, autoclaves. Particle Monitoring and HVAC requalification. Review of qualification documentation using QMS and Document Management Systems such as Veeva. Prepare & update GMP standard operating procedures& templates. Collaborate effectively within cross functional project teams to meet tight deadlines. About You - Skills & Experience Tertiary qualifications in Engineering or Science related discipline. Minimum of 5 years' 'hands on' Validation experience in GMP environment. Sound experience in the pharmaceutical/medical device industry. Solid technical writing skills and attention to detail. Proven ability to work under strict guidelines and pressured timelines. Excellent organisational and time management skills. Prepared to work independently and part of a team. Culture & Benefits This is an excellent opportunity for a Validation Specialist to join global pharmaceutical organisation and be responsible for all qualification and documentation review for major global project. This is an Excellent Contract Opportunity requiring Immediate Start. Will consider WHV Applicants who can work the full 12 months. How to Apply To apply for this opportunity, please click on the APPLY NOW button and forward your CV in MS Word. For a confidential discussion, please contact Sue Campbell on 0417 994 917 or call Maria Julienne on 0491 694 371. NB - Only shortlisted candidates will be contacted.
