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. 

Your role at Baxter:

Manage and coordinate routine activities and projects within the Manufacturing Quality Assurance team. This will include such activities as printed material control management, retention sample management, and nonconformance and CA/PA management while assuring compliance with established standards, regulations, specifications, and SOPs. Ensure that in process materials, finished products, packaging operations, and batch record documentation is in compliance with internal corporate/division/plant quality control programs, current Good Manufacturing Practices, current Good Documentation Practices, and external regulations. Assure the safety and quality of the products, processes, and systems.

Your Team

Baxter is focused on saving and sustaining lives by finding solutions to sophisticated problems. Every single day, the manufacturing team strives to create quality products for our customers—and are sometimes met with unforeseen issues to tackle. The high-caliber talent at Baxter meets these challenges head-on, as a team, to create products with the customer's needs top-of-mind.

We build relationships with each other to get work done.

We provide opportunities for you to continue to learn through training, conferences, certifications, and support for advanced degrees. Growth from role to role or level to level is encouraged and is supported by management to ensure employees are consistently engaged with their work.

What you'll be doing:

• Will interact with manufacturing and supervision on a daily basis to address quality process or batch related concerns.
• Performs process compliance audits of all manufacturing areas to ensure quality of product/process is achieved.
• Develops, assigns and implements systems, procedures and policies to assure compliance with cGMP's and FDA regulations and company policies and procedures. Assess all plant systems, operations, products, processes, procedures, and documentation for adequacy and effectiveness to ensure Quality and Regulatory Compliance related to CA/PA.
• Applies problem solving logically and in an organized manner. Must have experience with Root Cause Analysis tools and the ability to apply tools to plant scenarios.
• Manages a team of individuals to drive correction, prevention, and improvement throughout the plant. Is responsible for results in terms of timeliness and conformance to regulations and Baxter quality policies.
• Maintains appropriate quality metrics for trend analysis and Management Review.
• Must have good working knowledge of plant systems, processes, procedures, documentation, and products.
• Plays an active role on quality management teams within the organization.
• ​Must be able to manage multiple tasks and projects simultaneously.
• Manage activities of self and Technicians in achieving defined safety, quality, and production goals.
• Manages the control and storage of released printed materials and retention samples.
• Should be able to communicate at all Plant and Divisional levels.
• Assist in external and internal audits by collecting relevant information such as SOP’s and routers.
• Performs process compliance audits for areas of responsibility.

What you'll bring;

• Bachelor’s degree required, preferably in engineering or science. 3-5 years experience in Quality, Manufacturing or related field.
• Drives efforts to identify and implement process efficiencies in order to achieve established release goals. 
• Seeks new ways to improve and streamline current business and system processes. Identifies, manages, and where appropriate, leads multiple process/product improvement projects with the objective of achieving quality, efficiency and cost improvements.
• Works with minimal supervision.

#IND-USOPS

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The successful candidate for this job may be required to verify that he or she has been vaccinated against COVID-19, subject to reasonable accommodations for individuals with medical conditions or religious beliefs that prevent vaccination, and in accordance with applicable law.

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.

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Pay Transparency Policy

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
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