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This is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives.
Job Responsibility
Operate as part of the Sterility Assurance group to perform: Quality System & Regulatory Compliance: Maintain alignment with EU GMP & Guidelines
Sample preparation and processing of biological indicators
Carry out environmental monitoring for classified areas
Support with atypical sterilisation investigations
Investigation and communication of Out of specification results and the identification and implementation of CAPA
Support for projects relating to environmental monitoring
Compliance with EHS/GMP/GDP/Company and corporate policies and external regulatory requirements
Other Activities as deemed to be required to support the Thetford manufacturing operation
Requirements
Degree in Microbiology, Biomedical Science, Bioscience OR Pharmaceutical Science
Working in an environment where accuracy, numeracy, clear documentation and attention to detail are key requirements
Flexibility in working hours to suit business needs, may include early mornings, evenings and weekends periodically