About the Company: Operating as a major global pharmaceutical manufacturer with with global sites worldwide, our client is well known for its growth and innovation and is an Australian iconic brand in the marketplace. Due to new approved projects, an opportunity has arisen for a Project Engineer to be responsible for validation activities for a wide range of capital based projects. Reporting directly to the Project Manager, key duties include the following: About the Opportunity: Prepare qualification documentation ensuring IQ OQ documents meet TGA & FDA regulatory requirements. Validation & execute IQ & OQ protocols, preparing validation reports. Ensure all documentation meet GMP, TGA & FDA requirements. Coordinate project timelines for monitoring & qualification activities. Manage all aspects of CAPEX based project activities from design, project scoping, procurement, installation & commissioning. Effectively work with key internal & external stakeholders. About You: Tertiary qualifications in Engineering.(Chemical or Mechanical). Pharmaceutical/biotechnology or medical device industries. Sound 3 to 5 years engineering & validation experience. Sound GMP, TGA & FDA regulatory requirements. Project Management skills from start to finish. Well developed interpersonal & communication skills. Ability to liaise at all levels. Culture & Benefits: This is an Excellent Contract Opportunity for a talented Project Engineer with sound pharmaceutical & GMP experience t o further develop their skills & experience & join a global pharmaceutical manufacturer for new and ongoing CAPEX project work. This role requires an Immediate Start. How to Apply: To apply for this position, please click on the Apply Now button below and please submit your CV in MS Word. Contact Details: To find out more information or for further discussion, please contact Sue Campbell on 0471 994 917 or Maria Julienne on 0491 694 371. NB - Only shortlisted candidates will be contacted.
