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.
As a Quality Compliance Technician, you will proactively support our Baxter Thetford Plant's Quality Management System (QMS) process for receiving inspection of raw materials and issuance of codes specific materials to production lines. Your core and responsibility ensures that incoming materials meet the required quality standards and specifications before they are accepted and stored or used in the production process.
We draw energy from working in a plant where there are opportunities to collaborate. As the company evolves, so does the way our team approaches work as it strives to create top-of-the-line products. This means the role is fully based on site at our Thetford Manufacturing plant.
Working hours for this role are 37.5 hrs per week, Monday to Friday offering a competitive salary as well as some great benefits:
• days annual leave + bank holidays
• Employee discount scheme
• Blue light card
• Progression opportunities
• Subsidised canteen
• Westfield healthcare
• Up to 8% pension contribution
• Employee assistance programme
What you'll be doing
* Receiving inspection duties of incoming components. This includes:
* Sampling, inspection, release or rejection of materials
* Verification of all relevant documentation, such as certificates of origin, and packaging labels, are complete and accurate.
* Record inspection results, including any defects or non-conformities found
* Maintain accurate and complete quality control records
* Collaborate with production teams to ensure that incoming goods meet production requirements and specifications
* Proofread of label copies
* Proofread and issue batch paperwork and truck cards for Production
* Maintain secure storage and accountability of Code Specific Materials in the label room and in MILD
* Issue code specific materials to production as per production plan & receive and return to stock those code specific materials that are returned from Production
* Provide training for Operators on handling
What you'll bring
* Degree qualified in a Science or Engineering based subject
* ideally experience within Medical Device, Pharmaceutical or Biologics industry
* You will have the experience and ability to communicate with cross functional teams
What happens next?
Our Talent Acquisition team will review your application and be in touch within 2 weeks.
IND-UKOPS
Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
Recruitment Fraud Notice
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