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QA Releaser (12 Month FTC) Full Time

at Baxter International in London (Published at 23-05-2020)

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We believe every person deserves a chance for a healthy life, free from illness and full of possibility. We see a world full of healing, with viable care options available to those with limited choices today. We envision new ways of providing physicians, pharmacists and nurses with technologies that not only treat chronic diseases, but also work to prevent them. We?re looking for team members who are motivated to learn, grow and innovate, while making a meaningful difference for millions of people around the world.


Learn more about how Baxter is At the Intersection of Saving and Sustaining Lives.


Quality Assurance Releaser


We are currently recruiting for a Quality Assurance Releaser to undertake the assessment programme for the release of manufactured products for our Croydon Manufacturing plant. This a full-time position and the candidate will be actively involved in the site?s microbial monitoring and validation, and will be reporting to the QA Manager.


Role 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, report 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 QA Pharmacist.

  • 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 site?s microbial monitoring, validation and other programmes as required by the QA Manager.


Skills and Experience


  • Membership with the General Pharmaceutical Council.

  • 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


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 Americas_TTA@baxter.com and let us know the nature of your request along with your contact information.



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