Sterility Assurance Microbiologist at Baxter International Inc.
England, East Suffolk - England, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

18 Nov, 26

Salary

0.0

Posted On

20 Aug, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Biotechnology

Description

About the job


This is where your work makes a difference.


At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.


Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.


Here, you will find more than just a job—you will find purpose and pride. 


Baxter Thetford have a fantastic opportunity for Microbiology Engineer to join their Microbiology team to complete project work related to heat studies and environmental monitoring.


 


This is a fantastic opportunity for a microbiologist to gain wider exposure working for a global pharmaceutical company. You will work closely with various partners throughout the plant, working primarily with the sterility engineering team as well as analysts within the laboratories.


 


We offer some fantastic benefits which are listed below;

  • 25 days annual leave + bank holidays
  • Employee discount scheme
  • Blue light card
  • Fantastic internal progression opportunities
  • Subsided canteen
  • Westfield healthcare
  • Up to 8% pension contribution
  • Employee assistance program




Essential Duties and Responsibilities:




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.


Responsibilities
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