QA Releaser Stockport, England
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 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’s 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 ‘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.
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
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
#IND-UKOPS
#IND-UKCOM
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 [email protected] 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.
