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.Are you passionate about ensuring products are delivered to customers in the best quality possible? As a Quality Assurance Releaser you will take responsibility 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, 07:00-15:00 ,10:00-18:00 and 14:00-22:00 on rotation.Essential Duties and Responsibilities.To undertake and successfully complete an in-house competency 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.Communicate 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 mannerTo participate in the organisation and delivery of in-house education and training sessions.GEMBA pre audits carried out weekly in areas such as the clean-room, preparation room and label and release, to ensure SOP and GDP are followed correctly.To support with Environmental Monitoring activities and data trending.Education and/or ExperiencePharmacy degree or similar science degreeGood 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 unitAbility to read, interpret and transcribe data accuratelyCustomer orientatedWhat are some of the benefits of working at Baxter?Competitive salary, plus a competitive benefits packageProfessional development opportunitiesHigh importance placed on work life balanceCommitment to growing and developing an inclusive and diverse workforce#LI-MT1#IND-UKOPS#IND-UKCOM#LI-BAXGENEqual Employment OpportunityBaxter 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 AccommodationsBaxter 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 here and let us know the nature of your request along with your contact information.Recruitment Fraud NoticeBaxter 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 .
