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\xe2\x80\x94where your purpose accelerates our mission.

Summary

We are currently recruiting for a Quality Assurance Releaser to undertake the assessment programme for the release of manufactured products for our Stockport Manufacturing plant. This a permanent, full-time position and will be actively involved in the site\xe2\x80\x99s microbial monitoring and validation and will be reporting to the QA Manager.

The role will be on a shift rotation basis, one week 6am to 2pm and then the following week 2pm and 10pm, 37.5hrs a week total, Monday to Friday.

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 \xe2\x80\x98in-process\xe2\x80\x99 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.

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\xe2\x80\x99s microbial monitoring, validation and other programmes as required by the QA Manager.

Skills and Experience

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

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

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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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