QA Releaser Compounding bei Baxter International

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. 

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. The QA Releaser will report to the Compounding QA Supervisor ensuring continuous compliance of the Compounding Unit to cGMP and “Specials” manufacturing requirements, local procedural requirements and Baxter Corporate policies.

The hours are Monday - Thursday 06:00-14:00 / 14:00-22:00. You will receive a competitive salary and a weekly shift allowance of £45.35.

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 programme

Essential Duties and Responsibilities

• 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.

Qualifications

• Degree or BTEC (or equivalent) in Pharmaceutical or Science related subject preferable but not essential
• At least 2 years experience in a GMP environment
• 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

#IND-UKOP

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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