QA Releaser

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.

Summary

We are currently looking for a QA Releaser to work from our high performing site in Oxford.

This a full-time position and the candidate will be actively involved in the reviewing and releasing of ‘specials’ product and accurately maintain technical data to control the production process. The position holder is expected to possess technical skills and knowledge of the unit’s activities, including aseptic compounding, facility and equipment management of workflow in line with MHRA Manufacturing License and Quality Systems requirements. The position reports to the QA Manager.

The shifts will be working between 07:00-15:00, 10:00-18:00 ,15:00-2300 Monday to Friday on a week by week rotation.

Essential duties & Responsibilities

• To undertake and successfully complete an in-house competency assessment programme for the release of manufactured products.
• Comply with any restrictions that may apply when release of manufactured products.
• Release of manufactured products according to defined procedures.
• Perform ‘in-process’ checks and report any errors according to defined procedures.
• To work as an integral member of the quality team to deliver a timely, safe, quality and aseptic manufacturing service to meet customer needs.
• To participate in the development and implementation of Standard Operating Procedures and to ensure processes and procedures are kept up to date.
• Assisting with daily workload scheduling alongside other members of the QA team.
• 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.
• Exposure to other activities / projects within Quality Assurance!.

Qualifications & Experience

• Good understanding of the Regulatory requirements involving pharmaceutical manufacture. Specials licence requirements and compounding/aseptic process experience is desirable
• Strong interpersonal skills to collaborate efficiently with all members of the unit
• Highly motivated
• Meticulous in attention to professional standards
• Respond well to time constraints with an ability to work in a dynamic, fast-paced, and dedicated environment.
• Customer orientated
• Pharmacy degree or equivalent experience, similar science degree.

What are some of the benefits of working at Baxter?

• Competitive total compensation package
• Professional development opportunities
• High importance placed on work life balance
• Commitment to growing and developing an inclusive and diverse workforce.
• Baxter is committed to growing and developing an inclusive and diverse workforce – you can read more about our specific values here https://www.baxter.com/careers/inclusion-diversity.

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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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