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.
We are searching for candidates that have at least 2 years GMP experience and a scientific qualification. Please only apply if you meet this criteria.
The hours are Monday - Friday rotating weekly, 06:00-14:00 / 14:00-22:00. (Please note that that the PM shift will change to 13:00-21:00 in November) You will receive a competitive salary of 33,729 PLUS 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 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
#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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