Quality Assurance Releaser (12-month FTC)

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

Job Description

Are you passionate about ensuring products are delivered to customers in the best quality possible? As a Quality Assurance Releaser you will take ownership for the completion of reviewing orders and releasing products. Accurately maintains technical data to control the production process. Provides technical skills and knowledge for all aspects of the units activities, including aseptic compounding, facility and equipment management and management of workflow in line with MHRA Manufacturing Licence and Quality System requirements.

Monday to Friday, 8am to 4pm or 10am to 6pm on rotation, with occasional requirements to work on 2pm to 10pm shift.

Essential Duties and Responsibilities.

• To undertake and successfully complete an in-house proficiency assessment programme for the release of manufactured products.
• Release of manufactured products according to defined procedures.
• Perform ‘in-process’ checks, report and report any errors according to defined procedures.
• Connect with the warehouse team in regards to timings of released products to ensure efficient dispatch.
• To work as an integral member of the quality team to deliver a timely, safe, quality aseptic manufacturing service to meet customer needs.
• To ensure that all documentation is complete and kept in a tidy and orderly manner
• To participate in the organisation and delivery of in-house education and training sessions.
• GEMBA pre audits conducted weekly in areas such as the clean-room, preparation room, and label and release, to ensure SOP and GDP are accurately followed.
• Support with EM activities when vital.

Education and/or Experience

• Pharmacy degree or equivalent experience in a related scientific field
• Good understanding of the Regulatory requirements involving pharmaceutical manufacture. Specials licence requirements and compounding/aseptic process experience is desirable.
• Ability to communicate clearly and optimally in a timely manner with all members of the unit
• Ability to read, interpret and transcribe data accurately
• Customer orientated

What are some of the benefits of working at Baxter?

• Competitive salary, plus a competitive benefits package
• Professional development opportunities
• High importance placed on work life balance
• Commitment to growing and developing an inclusive and diverse workforce

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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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