CPS Support Operations

Job Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Company Description In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 62,000 staff across a network of more than 1000 independent companies in over 62 countries and operating more than 900 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services. Job Description The Clinical Protein Suite (CPS) Support Operations Technician role is a fundamental support function within our client’s state of the art research and development facility in Melbourne CBD. The CPS is a GMP pilot facility which produces early phase material for clinical studies. Activities within the CPS require operational support; this may include equipment collection, washing, sterilisation and consumable/equipment kitting. Support Areas for the CPS Bulk Wing Equipment Wash. Bulk Wing Equipment Preparation. Bulk Wing Equipment Store. Filling Wing Equipment Wash/Prep. Filling Wing Equipment Store. Filling Wing Material Store. Filing wing Solution Preparation (as required). Routine tasks include Decartoning of consumables and affixing of identifying labels as appropriate. Movement of consumables into the facility to internal storage locations. Subsequent kitting of consumables and equipment preparation for production operations. Restocking of facility gowns etc. Potential ad hoc requirement for waste management. Collection & preparation of equipment for cleaning and/or sterilisation. Equipment washing and drying. Equipment sterilisation. Ensuring compliance with the client site's OHS / QA Systems and regulatory requirements. Data and Reports All activities will be captured via electronic record systems that detail the equipment and consumables (if applicable) used and adherence to specified method. Clean equipment must be labelled with date of clean or if sterile equipment then date of sterilisation and log number. People performing the above activities will report to the Facility Support Lead. Qualifications Previous GMP experience of 2 or more years (preferred). Laboratory Skills TAFE certificate / Diploma in an appropriate scientific field preferred. Very good understanding of requirements for working in a GMP environment is essential. Willing to operate in a flexible manner and be able to switch priorities at short notice. Good team player, organised, accurate, have strong documentation skills. Good communication skills both internally and externally. Capable of collaborating with cross-functional teams. Demonstrate problem solving in delivering process and analytical understanding. #J-18808-Ljbffr