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 Production Operator, your mission is to directly execute all manufacturing activities associated with the production of high-quality IVD (In Vitro Diagnostics) products at Grifols Australia, in full compliance with internal procedures and international quality standards, to help ensure the health and safety of patients worldwide.

SKILLS

• Excellent attention to detail and high standards of accuracy
• Good organizational skills and a strong work ethic
• Comfort with digital tools and manufacturing systems (SAP R3 experience desirable)
• Knowledge of GMP, ISO 13485, and hygienic practices

QUALIFICATIONS

• Recent graduate or 1–2 years of experience in a regulated production environment (medical device, pharmaceutical, biotech, etc.)
• Demonstrated understanding of quality systems and manufacturing operations
• Availability to work shifts as rostered

EDUCATION

• Relevant secondary or tertiary education in science, biotechnology, or related fields

• You will follow approved manufacturing and testing instructions to produce IVD products (e.g., Reagent Red Cells, Solutions, Gel Cards).
• You will perform small- and large-scale formulation and filtration of solutions and gels.
• You will operate purpose-built equipment to dispense and pack finished goods.
• You will carry out in-process quality control tests using approved laboratory equipment.
• You will accurately record material movements in SAP R3.
• You will collect QC samples for environmental monitoring, bioburden, and serological testing.
• You will ensure cleanliness and maintenance of manufacturing equipment and areas according to SOPs.
• You will support validation and qualification of equipment and processes alongside the Production and Validation teams.
• You will contribute to continuous improvement initiatives and harmonization efforts with Grifols Diagnostics global standards.
• You will perform all tasks in accordance with cGMP, ISO 13485, OHS policies, and internal procedures.
• You will cooperate actively in OHS activities, report hazards, and ensure a safe work environment.
• You will support documentation, including completion of records and updates of SOPs when necessary.