QA Releaser

---

Job description

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 to 15:00 or 10:00 to 18:00 Monday to Friday, on a weekly 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.
• To participate in other site's activities as required by the QA Manager.

Qualifications & Experience

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

#IND-UKOPS

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

053370