IVD Pharma Production Operator – GMP/ISO 13485

Grifols, S.A; Australia; Híbrido; AUD 55.000 - 75.000; Jornada completa

Descripción de la vacante

Grifols Australia is seeking a Production Operator to drive daily manufacturing plans and ensure delivery of high-quality IVD products to patients globally.

You will work in a GMP/ISO 13485 environment, log materials in SAP R3, and collaborate with engineers and senior management to optimize processes and support Grifols global standards.

The role offers an opportunity to contribute to one of the world’s leading pharmaceutical companies with a focus on quality and continuous improvement.

Formación

• Proven ability to work under strict safety guidelines (OH&S) and compliance frameworks (GMP/ISO 13485) within a regulated manufacturing environment.
• Familiarity with SAP R3 or similar systems is highly valued.
• Background or certification in manufacturing, laboratory operations, life sciences, engineering, or a related industrial discipline.

Responsabilidades

• Manufacture high-quality IVD products (Reagent Red Cells, Solutions, and Gel Cards) following approved testing and formulation.
• Operate purpose-built equipment to dispense and pack finished goods and log material movements in SAP R3.
• Conduct in-process quality control tests and collect environmental, bioburden, and serological QC samples.
• Uphold ISO 13485, GMP, and Grifols SOPs to maintain a pristine, compliant facility.
• Collaborate with supervisors, engineers, and senior management to optimize processes and drive continuous improvement.

Conocimientos

Attention to detail

Team player

Lab equipment familiarity

ERP software proficiency

Educación

Manufacturing/Lab operations

Herramientas

SAP R3

Descripción del empleo

Grifols Australia is seeking a Production Operator to drive daily manufacturing plans and ensure delivery of high-quality IVD products to patients globally.

You will work in a GMP/ISO 13485 environment, log materials in SAP R3, and collaborate with engineers and senior management to optimize processes and support Grifols global standards.

The role offers an opportunity to contribute to one of the world’s leading pharmaceutical companies with a focus on quality and continuous improvement.