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QA Releaser (Compounding)

https://www.baxter.com/ Logo

Baxter

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Location:
United Kingdom , Thetford

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Contract Type:
Not provided

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Salary:

Not provided

Job Description:

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. We are recruiting for QA Releasers to join our Compounding team in Thetford. We compound medications classified under broad therapies of Chemotherapy, Nutrition and IV Antibiotics. You will be joining an organisation that saves and sustains lives globally.

Job Responsibility:

  • Support manufacture of aseptically products by making QA decisions during batch manufacturing and ensuring GMP is adhered to at all times
  • Complete documentation and batch reviews as required
  • Inspect and release final products as per Company policies
  • Support Production in the review and post compounding check operations
  • Support delivery of product release targets, including ensuring timely batch review activities and batch disposition of any deviations with impact to product release
  • Proactively identify and support implementation of continuous improvement opportunities in QA and Operations
  • Ensure timely completion of all GMP commitments
  • Ensure timely communication of significant GMP and product quality issues to QA Management
  • Align with EHS/GMP/GDP/Company and Corporate policies and external regulatory requirements
  • Ensure facility and process compliance through attendance of Gemba activities, identifying actions and facilitate implementation
  • Implement and sustain EMS principles
  • Support release and Quarantine area issues, where required
  • Facilitate the implementation of an ‘Audit Ready’ compliant site which is always ready for MHRA, corporate, internal or 3rd party audit
  • Support the completion of audit findings and fully investigate to find the root cause and actions to address the audit findings are carried out in a timely manner.

Requirements:

  • Degree or BTEC (or equivalent) in Pharmaceutical or Science related subject preferable but not essential
  • At least 2 years experience in a GMP environment is essential
  • Strong work ethic and able to work flexibly to meet the needs of the business
  • Uncompromising commitment to Quality
  • Ability to communicate effectively to all levels of the organisation
  • Committed and supportive teammate
  • Accurate worker with strong attention to detail
What we offer:
  • 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 programme
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer

Additional Information:

Job Posted:
January 09, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

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