Quality 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 (15-Month Fixed-Term Contract)

Hours: 37.5 hours per week
Shift Pattern: Full Rotation

• 6:00am to 2:00pm
• 2:00pm to 10:00pm

Please note: This role requires candidates to work both shifts on a rotating basis. We are unable to accommodate permanent early or late shift preferences.

About the Role

We're looking for a detail-oriented Quality Releaser to join our Quality team on a 15-month fixed-term contract. You'll play a key role in ensuring products are released safely, accurately, and on time, while maintaining the highest standards of quality, compliance, and customer satisfaction.

Working closely with Manufacturing and Quality colleagues, you'll support the review and release of products in line with GMP requirements, customer expectations, and company quality standards.

Key Responsibilities

Product Release & Quality

• Review and release products against approved specifications and customer requirements.
• Ensure products undergo all required inspections and release checks before approval.
• Verify compliance with GMP and quality system requirements.
• Assess deviations and non-conformances to ensure appropriate disposition decisions are made prior to release.
• Support the timely review and disposition of affected products, raw materials, and components.
• Maintain accurate and compliant quality documentation.

Quality Systems & Continuous Improvement

• Promote a culture of quality, compliance, and continuous improvement.
• Participate in quality review meetings and complete agreed actions within deadlines.
• Support standardisation and process improvement initiatives across the site.

Communication & Training

• Attend Quality team meetings and maintain a strong understanding of GMP requirements.
• Support training activities to ensure compliance with company and regulatory standards.
• Work collaboratively with Manufacturing and Operational teams to achieve quality and delivery objectives.

Compliance & Environmental Monitoring

• Review environmental monitoring data when required.
• Support compliance with manufacturing licence requirements and GMP standards.
• Contribute to Environmental Health & Safety (EHS) initiatives and safe working practices.

What We're Looking For

• Experience in a regulated manufacturing, pharmaceutical, healthcare, or quality environment.
• Understanding of Good Manufacturing Practice (GMP) requirements.
• Strong attention to detail and a commitment to quality and compliance.
• Experience reviewing documentation and making quality-based decisions.
• Excellent organisational and communication skills.
• A proactive approach to problem-solving and continuous improvement.
• Ability and willingness to work both shifts on a rotating basis (6am-2pm and 2pm-10pm).

Why Join Us?

This is an opportunity to make a real impact in a quality-focused manufacturing environment, helping ensure products meet the highest standards of safety, compliance, and customer expectations while developing your experience within a collaborative and supportive team.

 
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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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