QA Releaser

This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride. 

Quality Releaser

Overview

We are looking for a quality-focused and detail-oriented Quality Releaser to support the release of compounded products within our aseptic manufacturing environment. You will be responsible for conducting on-site quality checks, verifying batch and manufacturing documentation, and ensuring products are released in compliance with customer requirements, MHRA Manufacturing Licence standards, and Quality System procedures.

This role will work Monday - Friday on a rotating shift of 07:00 - 15:00; 10:00 - 18:00 & 15:00 - 23:00. 

Responsibilities

• Inspect and release manufactured products in line with approved procedures.
• Perform in-process checks, including facility, equipment, product, manufacturing, and documentation reviews.
• Verify customer orders and batch documentation prior to product release.
• Identify, report, escalate, and support the resolution of quality issues.
• Ensure all records are completed accurately and in accordance with ALCOA+ and Good Documentation Practice principles.
• Communicate with Logistics to support the timely dispatch of released products.
• Participate in weekly GEMBA walks and pre-audit checks.
• Work collaboratively with Manufacturing, Quality, and Logistics teams to deliver a safe, compliant, and efficient service.

Requirements

• Eligible to work in the UK on a full-time basis.
• English qualification equivalent to RQF Level 2, EQF Level 3, or SCQF Level 5.
• Good understanding of the compounding process.
• Strong attention to detail and commitment to quality.
• Ability to work independently and as part of a team.
• Effective communication, organisation, and time-management skills.
• Ability to accurately read, interpret, and record data.
• Basic knowledge of Microsoft Office applications.
• Science degree or NVQ Level 3 (or equivalent) in a science-related discipline.
• 2+ years' experience in an aseptic manufacturing environment.

What are some of the benefits of working at Baxter?

• Competitive total compensation package
• Professional development opportunities
• High importance placed on work life balance

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Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

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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