QA Releaser

Baxter; Stockport; Sur place; GBP 42 000 - 56 000; Plein temps

Avantages offerts par ce poste

Support for Parents

Continuing Education/ Professional Dev

Employee Health & Well-Being Benefits

Paid Time Off

Volunteer time

Diverse international team

Résumé du poste

Baxter is seeking a detail-oriented Quality Releaser on a 15-month fixed-term contract in Stockport. You will release products in line with GMP, support training, and collaborate with Manufacturing and Quality teams to ensure safety, quality and timely delivery.

The role emphasizes quality review, compliance with regulatory standards, and a proactive approach to continuous improvement within a manufacturing environment.

Qualifications

• Registered pharmacist in the UK with experience in drug products and final product release.
• Strong attention to detail and commitment to GMP compliance.
• Experience reviewing documentation and making quality-based decisions.

Responsabilités

• Release products in line with GMP requirements and company quality standards.
• Participate in quality review meetings and complete actions by deadlines.
• Support training activities to ensure regulatory and company standards compliance.
• Collaborate with Manufacturing and Quality teams to meet quality and delivery objectives.

Connaissances

Pharmacist UK registered

Detail oriented

Quality mindset

Documentation

Communication

Problem solving

Description du poste

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., Product Release & Quality

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., 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.

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. 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.

This is where you make a difference in our patients' safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people's lives.

Key Qualifications

• I am registered pharmacist in the UK with experience with drug products and final product release. I am very dedicated to my work and accurate in details to ensure correct assessment is provided to our customers to ensure patients' safety.
• Detail Oriented
• Continuous Learner
• Courageous
• Collaborative
• Critical Thinker
• Influential, 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).

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.

Benefits and Culture

• Support for Parents
• Continuing Education/ Professional Development
• Employee Health & Well-Being Benefits
• Paid Time Off
• 2 Days a Year to Volunteer, Hours: 37.5 hours per week
• Our company is enriched by a diverse population of individuals in more than 100 countries that work to solve, innovate, manufacture and drive better healthcare options for patients around the world.