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 looking for a Quality Associate, to initially cover maternity leave for 12 Months. The role will work onsite at our successful compounding manufacturing facility in Croydon.
The main objective of the QA Associate is to implement, maintain, and assist in the development of the Quality Management System (QMS).
QA Support on site in the following working pattern:
Monday to Friday 08.00 - 16.00 and 10.00 - 18.00 (weekly rotation)
Essential Duties and Responsibilities
Participate in CPI, complaints handling and investigation, non-conformance monitoring and trending.
Drive corrective and preventive action implementation.
Participation in preparation for audits and follow up and close out audit findings.
Participation in reviews of production processes (to meet regulatory and customer requirements)
Maintenance of SOPs
Conduct (once trained) relevant internal audits as defined by the relevant schedules or as the need arises.
Handle and coordinate the equipment calibration and maintenance programme.
Handle the Materials Management/Vendor Assurance process.
Preparation of Management Review, Capacity Analysis and Scorecard data
Process Improvement support.
Stability Maintenance Coordinator
Project and New initiatives support
Qualifications and Experience
Graduate Calibre/BTEC/NVQ or equivalent qualification.
Quality Assurance experience advantageous.
Experience working in a pharmaceutical/manufacturing environment.
Ability to communicate clearly and optimally, in a timely manner with all members of the unit.
Ability to complete records accurately and with sufficient detail using Good Documentation Practice.
To be a willing and active member of the QA team.
Ability to read, interpret and transcribe data accurately.
Dedicated to meeting the expectations and requirements of internal and external customers.
Ability to learn and retain new processes.
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 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 link here and let us know the nature of your request along with your contact information.
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