Releaser, QA

This is where you save and sustain livesAt 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.SummaryWe are currently recruiting for a Quality Assurance Releaser to undertake release of manufactured products from our high performing Compounding Unit in Stockport.This a permanent, full-time position and the candidate will be actively involved in the reviewing and releasing of ‘Specials’ product and accurately maintaining technical data to control the production process.  The position holder will be expected to undertake a program of training and maintain 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, working shifts covering twilight shift, between 6am to 2pm and 12pm to 8pm on a weekly rotation.Role ResponsibilitiesTo 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 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 the other members of the QA Team.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.To participate in other site activities as required by the QA Manager.Skills and ExperiencePharmacy 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 unitAbility to read, interpret and transcribe data accuratelyCustomer orientatedWhat are some of the benefits of working at Baxter?Competitive total compensation packageProfessional development opportunitiesHigh importance placed on work life balanceCommitment to growing and developing an inclusive and diverse workforce#IND-UKOPS#IND-UKCOMReasonable AccommodationsBaxter 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 Americas_TTA@baxter.com 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 Recruitment Fraud Notice. 053345

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Job Overview

ID:

508482

Date Posted:

Posted 2 weeks ago

Expiration Date:

05/02/2022

Location:

Stockport District

Salary:

Competitive

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