Releaser, QA

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Overview

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.

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Success Profile

What makes a successful Quality team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.

Detail Oriented
Continuous Learner
Courageous
Collaborative
Critical Thinker
Influential

Releaser, QA

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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.

We are seeking a Quality Assurance Releaser to join our Stockport Compounding site on a rotational shift of 6am-2pm and 2pm-10pm, Monday to Friday.

Product Release
- Rotational shift, 6am to 2pm and 2pm to 10pm alternating weekly.
- Responsible for ensuring that all product released meets specification and customer requirements.
- Responsible for ensuring that all product undergoes effective visual inspection, release checks and has been manufactured in compliance with GMP and quality system requirements.
- Responsible for ensuring no product is released before a formal assessment for the impact of the deviation is made and a disposition is approved.
- Responsible for ensuring the disposition of products and raw materials/components impacted by non-conformances is appropriately documented and completed in a timely manner.

Communication and Training
- Regularly communicates with all site staff regarding quality issues and promotes the quality system as a business process for improvement of customer satisfaction and regulatory compliance
- Attends and participates in QA Team meetings
- Ensures their own understand their responsibilities under the quality system regulations
- Ensures training is delivered with staff to enable them to complete their jobs in compliance with the Baxter quality systems and country regulations
- Supports the communication of changes of the quality system to staff, ensuring appropriate training programs are executed.
Quality System Measurement and Review
- Attends and participates in monthly quality review meetings when required
- Ensure assigned meeting actions are completed to agreed deadlines
Complaints
- Ensures all incidents reported by customers are appropriately escalated to line management
- Management of complaints using the pilgrim PMDA software if required
- Raising supplier complaints with Line management to address out of specification raw material issues
Non-Conformance and Corrective and Preventative Action (CAPA)
- Ensure that any failure to follow procedure or failure of product to meet specification is fully documented and investigated
- Initiation and investigation of Non-conformance/CAPA event reports as required
- Monitor all quality system processes to detect need for improvements
- Non-Conformance/CAPA owner and leader as required
- When required, ensure Non-conformance/CAPA investigations are completed and root cause identified and that appropriate actions are specified and completed according to agreed time frames
Change Control
- When required, maintain a local change control process to ensure all changes are fully documented
- Support the assessment for risk and impact prior to change implementation
- Support the implementation of changes as per impact assessment and in the appropriate time frame
Validation
- Responsible for Approval of validation protocols and reports if required
GMP and Facilities and Equipment Control
- Responsible for the Quality review of environmental monitoring results when required
- Support Environmental, Health & Safety (EHS) programme
Risk Assessment
Supports the site risk management process
Supports the update of risk assessments as a result of quality system measurement and review and change management.
Actively manages risks by identifying potential failure modes.

Audit Management
- Ensures that the facility is always ready for an internal, Corporate, MHRA or 3rd party audit
- Support the audit processes to ensure effective audit management

Document and Data Management
- Ensures there are no unauthorized changes to documents including creation of local documentation.
- Ensures all quality records are reviewed and that they are complete, comprehensive and legible and comply with good documentation practice.
- Ensures are quality records are retained in such a way that they remain complete, comprehensive and legible

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.

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.

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Address

Explore this location Baxter Healthcare Ltd, Chemotherapy Compounding Service Boundary Court Crossley Road
Stockport
Cheshire
SK45GA
United Kingdom Explore This Location

Hear from Our Employees

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.

Meet Christelle, Senior Quality Manager in Malta

“I was an Engineering Graduate with a Master's in Business Administration, and was more inclined toward working with people than with machines. When I came across an opportunity to work with Baxter as a Quality Engineer, it was the perfect combination: a manufacturing environment and a role that required me to collaborate with multiple teams daily. Baxter's mission of saving and sustaining lives gives me all the purpose and fulfilment I need.”

Meet Lorena, Senior QA Associate in London, UK

“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.”

Meet Gary, Quality Research Manager in Singapore

“I have always enjoyed working at Baxter and I find here to be a great place to work! Management truly cares for you, and invests time and resources to support your career goals and aspirations. My current role provides me the opportunity to work with culturally diverse teams, bringing different talents together, learning from one another and working toward a common goal and mission.”

Join Our Talent Community

We're grateful for your interest in a career with Baxter, and would like to get to know you. Joining our Talent Community is a great way to stay connected, learn more about Baxter, and help our recruiters find you if there's an opportunity that aligns with your background, skills and interests.

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Releaser, QA

Overview

Success Profile

Releaser, QA

Address

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Hear from Our Employees

Meet Christelle, Senior Quality Manager in Malta

Meet Lorena, Senior QA Associate in London, UK

Meet Gary, Quality Research Manager in Singapore

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Join Our Talent Community