QC Microbiologist

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

Summary

The microbiology analyst completes all laboratory testing and monitoring of the Pack rooms unclassified controlled areas and relevant critical systems.

They must work as part of a team to ensure the required testing is performed following established practices and within the required time frames. They are expected to be able to perform all testing within the laboratory. This can include testing within the Chemistry lab.

Working hours are Monday to Friday, 9am-5pm (with flexibility where required).

Essential Duties and Responsibilities

1. Perform microbiological testing of water systems and drug products.
2. Perform testing on samples from raw materials, In-Process, Release and stability.
3. Book in and control of samples.
4. Work with the team and QC Manager to organise work.
5. Perform support activities required for the function of the laboratory.
6. Conduct environmental monitoring of unclassified production area pack rooms.
7. Follow established procedures for performing activities in the laboratory.
8. Adhere to Good Quality Control Laboratory Practices (GLP) and maintain a clean work area.
9. Follow Good Manufacturing Practices (GMP) and Good Documentation Practice (GDP).
10. Conduct laboratory investigations / exceptions / NCR / CAPA.
11. Provide support for the QC Manager in any reasonable request relating to the laboratory operation.
12. Proactively drive Continuous Improvements and Digital Transformation within the QC footprint.
13. Provide support and training for others within the laboratory.
14. Review team members' lab testing.
15. Perform periodic review of relevant SOPs for the area.
16. Conduct Validation Maintenance of the Analytical methods used in the area.
17. Work with the wider teams throughout the business to provide support as required.

Qualifications and Experience

1. Continual Improvement driven / Change Agent personality essential.
2. Technical knowledge and experience in a regulated pharmaceutical microbiology laboratory environment.
3. Proficient in analytical weighing, sample dilutions, aseptic technique, pipetting technique, and plate reading.
4. Experience using the Vitek system.
5. Ability to react to unexpected situations and troubleshoot technical issues.
6. Understanding GMP requirements and Regulators Expectations.
7. Ability to work as part of a team in a dynamic, fast-paced laboratory environment.
8. Excellent communication and interpersonal skills, with a proactive approach to work.

What are some of the benefits of working at Baxter?

1. Competitive total compensation package.
2. Professional development opportunities.
3. High importance placed on work life balance.
4. Commitment to growing and developing an inclusive and diverse workforce.