Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
As a Production Operator at Grifols Australia, your mission is to directly execute manufacturing activities to ensure production goals are met and products are delivered to the highest quality standards. You will work with purpose-built equipment, follow Good Manufacturing Practices (GMP), and contribute to producing high-quality In Vitro Diagnostic (IVD) products such as Reagent Red Cells, Solutions, and Gel Cards.

SKILLS:

• Strong attention to detail
• Ability to follow procedures precisely
• Good communication and teamwork skills
• Willingness to learn and adapt
• Awareness of hygiene and safety practices

QUALIFICATIONS:

• Any experience in pharmaceutical, biotechnology, or medical device manufacturing is a plus, but not required
• Familiarity with GMP, ISO 13485, or SAP is an asset
• Open to recent graduates or individuals seeking a new direction in a regulated manufacturing environment

EDUCATION:

• Secondary education (e.g., Year 12 or equivalent)
• Further studies in science or technical fields are a plus but not essential

• You will follow approved manufacturing and testing instructions to produce IVD products.
• You will operate equipment to dispense and package finished goods.
• You will perform large- and small-scale formulation and filtration of solutions and gels.
• You will accurately record material movement using SAP R3.
• You will carry out in-process quality control checks and collect QC samples.
• You will maintain a clean and hygienic production environment in accordance with SOPs.
• You will follow OH&S policies and GMP principles at all times.
• You will work closely with Production Supervisors and Engineers on process improvement and validation initiatives.
• You will support document maintenance and provide valid and reliable data.
• You will contribute to safety initiatives by reporting hazards and participating in drills.