QC Chemistry Technician

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. 

Our Thetford Plant is looking for a QC Chemistry Technician to join their raw material sampling team sampling all incoming raw materials upon warehouse receipt.

The role is Monday – Friday, 37.5 hours per week , 09:00-17:00. You will receive a competitive salary and we offer the below benefits:

• 25 days annual leave + bank holidays

•  Employee discount scheme

• Blue light card

• Progression opportunities

• Subsided canteen             

• Westfield healthcare

• Up to 8% pension contribution

• Employee assistance programme

What you'll be doing

• Ensure all incoming raw materials are inspected and sampled in accordance with all applicable SOPs and instructions.

• Inspect containers; verify accurate label information, lot numbers, and associated paperwork.

• Ensure accurate, timely entries are made in electronic laboratory notebook, LIMS and/or paper documentation.

• Perform regular routine cleaning tasks on the chemical sampling booth and surrounding work area.

• Support QC laboratory with reagent preparation, testing, sample handling when required.

• Be responsible for equipment. Perform calibration checks in accordance with procedures. Ensure that equipment is operated and maintained correctly.

• Support with daily activity scheduling and planning when required.

• Involvement with the Quality Management System (QMS), such as deviations, CAPAs, effectiveness checks, and laboratory investigations when required.

• Support document updates, changes controls, and successfully handle timelines for implementation of changes when required.

• Assist with internal, customer, and regulatory audits; complete any assigned action items in a timely manner.

What you'll bring

• Previous experience in a GMP environment.

• Excellent Attention to Detail

• Experienced in manual handling

• Highly experinced with visual inspections

• Ability to learn and retain new skills and simple process operations.

• Ability to communicate effectively.

• Ability to integrate well within an established team in a fast-paced environment

Thank you for your interest in Baxter, and we look forward to hearing from you!

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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.

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