Supervisor Release 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

Supervisor Release QA

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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.

THE ROLE

Lead, supervise, coach and coordinate a team of employees to achieve the objectives of the department(s) for which he/she is responsible. This is achieved by delivering quality products at the best possible cost, in a safe and serene environment.
He/she is responsible, at his/her level, for monitoring and implementing the company's policy on employee well-being and safety.
Responsible for the management and control of finished product release activities (sterile drugs and medical devices).
Lead finish product release process improvements, both locally as globally driven initiatives.

ESSENTIAL DUTIES & RESPONSIBILITIES

Responsible for the management and control of finished product release activities (sterile drugs and medical devices).
Responsible for the coordination and planning of batch file review activities of the complete Quality Assurance Release team.
Monitor and improve the release performance of the Quality Assurance team. Responsible for KPI (Key Performance Indicators) of both the release process (sterile drugs and medical devices) and release team to be submitted to the Region/Global.
Facilitate interactions of and ensure appropriate linkage with different stakeholders : Manufacturing, Supply Chain, Contract Manufacturing Organizations/3rd party suppliers, Product development and Quality Assurance team.
Assure establishing all regulatory aspects (documentation and procedure updates, quality agreements,..).
Support external and internal audits with release activities in scope, as auditee and auditor
Participate in quality training development and deliver quality training like GMP.
Participate in the Enterprise Management Systems and 6S implementation
Lead finish product release process improvements. Implement both locally as globally driven initiatives for improvements.

QUALIFICATIONS

Degree in Science or Engineering; advanced degree preferred
Proven experience in a similar or equivalent role and in people management.
Commitment to quality. Knowledge of GMP (EudraLex Volume 4) and of directives and regulations applicable to medical devices.
Excellent knowledge of quality systems and compliance.
Experience in project management.
Fluency in French and basic English is a must
Problem-solving and analytical skills and excellent communication and presentation skills
Critical and inquisitive mind
Resistant to stress & demonstration of flexibility in times of change

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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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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Supervisor Release QA

Overview

Success Profile

Supervisor Release QA

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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