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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. This 12‑month parental leave cover allows you to join an encouraging, cooperative team working Sunday through Thursday. Your expertise will affect the quality and reliability of life‑saving therapies. You will experience diverse microbiological testing and aseptic manufacturing processes, while helping Baxter maintain its dedication to excellence and innovation.
Job Responsibility:
Actively participate in Microbiology team meetings, contributing to discussions that build daily priorities, workload distribution, and problem‑solving approaches
Support aseptic manufacturing operations by following rosters set by Microbiology management, while remaining flexible to take on additional assignments when required
Perform microbiological testing adhering to the highest standards, guaranteeing accuracy, conformity, and consistency throughout all procedures
Complete, document, and communicate scheduled testing in line with established protocols and agreed timelines, maintaining transparency and accountability
Drive the timely completion of Change Controls, Validation protocols, and other critical microbiology activities that support manufacturing and quality assurance
Show proficiency in microbiological testing for Manufacturing and Pharmacy Services, maintaining strict adherence to procedures and regulatory requirements
Perform routine and investigational water testing across the facility, providing valuable insights into process control and compliance
Liaise closely with Manufacturing, Pharmacy Services, and QA teams to communicate results, resolve issues, and strengthen adherence to standards
Maintain laboratory equipment, consumables, media, and reagent stocks to ensure seamless operations and uninterrupted workflow
Ensure calibrations and validations of laboratory equipment are performed according to specifications, supporting accuracy and reliability in testing
Coordinate maintenance and repairs for laboratory equipment, ensuring issues are addressed promptly to minimize disruption
Conduct real-time risk evaluations in manufacturing cleanrooms, supporting proactive sterility assurance and adherence to regulatory standards
Participate in laboratory cross‑training, sharing knowledge and providing support to fellow team members to build collective capability
Remain up to date with microbiology techniques relevant to Baxter’s operations, supporting the preparation of process specifications and operating procedures to guarantee suitability and adherence
Provide support in testing, troubleshooting, evaluation of results, and trending, helping to find opportunities for improvement and efficiency
Contribute to preparations for internal, external, and corporate regulatory audits, particularly in relation to microbiology and associated areas of activity
Suggest improvements to laboratory practices and procedures to align with GMP, regulatory requirements, and guideline standards
Adhere to Environmental, Health & Safety guidelines at all times, ensuring a safe and compliant working environment
Complete all required training in BAXU within scheduled timelines, with training plans adjusted as necessary based on analyst experience and laboratory needs
Perform other duties as assigned by the Microbiology and Sterility Assurance Manager, supporting the overall success of the team
Requirements:
Bachelor’s degree or equivalent experience in Microbiology, Biotechnology, Life Sciences, or a related field (essential)
Minimum of 2–3 years’ experience in a microbiology laboratory within a GMP, pharmaceutical, or medical device environment
Strong knowledge of aseptic techniques, sterility assurance, and microbiological testing methods
Familiarity with regulatory requirements (e.g., GMP, ISO standards) and audit processes
Proficiency in laboratory equipment handling, calibration, and validation
Strong communication and collaboration abilities, capable of coordinating efficiently across QA, Manufacturing, and Pharmacy Services
Strong problem‑solving and troubleshooting abilities in microbiological testing