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Director, Quality Manufacturing Compliance Support

at Baxter Healthcare Corporation in Deerfield, Illinois, United States

Job Description

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
This is where your creativity addresses challenges
You are creative, thorough, and a heads-down do-er. You embrace a challenge and truly apply the collaborative powers of your team to produce great results. You are motivated by work that is never the same from one day to the next. As a Director, Manufacturing Quality Compliance Support, you are unafraid of navigating through necessary internal processes to facilitate a product you deeply believe in. You can absorb and act on complex procedures and data and train your team or peers if needed. You take pride in getting things done quickly without sacrificing safety or quality.
Your Team at Baxter
Within Quality, every role makes a difference. Products that Baxter makes are shipped worldwide for patients in need. Whether it's building a new process from scratch or facing a never-before-seen production hurdle, individuals within Quality are given the trust and opportunity to bring creativity to the table. Regardless of your specific role with a product, it is sure to touch a portion of our global operation.

The mission of Baxter is to save and sustain lives. This mission is embedded into everything we do. This means if there is a decision to be made where quantity and quality are at odds, we will always choose quality. Our patients come first, always.

The Quality function values both working together as a team and independently. We draw energy from working in a plant or an office where there are opportunities to collaborate. As the company evolves, so does the way our team approaches work as it strives to create top-of-the-line products.

We build relationships with each other to get work done. Building these relationships is easy because we all share common traits of being reliable, ethical, and caring. We lean on our colleagues for their expertise and hold each other accountable. We feel empowered to speak up when there's a new insight or opportunity to improve something. This open dialog builds trust within the team and helps create a better product for our customers.
What you'll be doing
Develops the strategy for the Manufacturing Quality Operations Support team. Works with other SMEs such as technical experts to drive global standardized processes, address issues for problem solving and create projects and standardizations and improvements within the businesses.
Manages a team of technical experts in the areas of manufacturing product and process controls, sterility assurance and other compliance focused topics including visual inspection and particulate control.
Develops the Sterility Assurance competencies and provide knowledge expertise of the corporation. Train SME's within the broader business segments. Shares sterility assurance knowledge broadly to drive innovation and partnership with Research and Development, Quality and Manufacturing organizations.
Identifies and manages continuous improvement projects that may span multiple business segments with the objective of achieving quality, reliability and cost improvements.
Develops budget for organization and ensures adherence to budget.
Manages overall coaching, training, development, and succession plans for the team.
What you'll bring
Significant experience (10+ years) in Quality, Regulatory, and/or Manufacturing. 7+ years of management experience.
Technical experience in drug, biologics, and medical device industry.
A degree in a life science or engineering discipline is required; an advanced degree is preferred.
Experience working in a operations manufacturing and or plant experience
Experience leading a Quality organization; strong ability to motivate and lead a diverse team with varying levels of experience while also collaborating with colleagues across the... For full info follow application link.

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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Job Posting: 12002235

Posted On: Jun 25, 2024

Updated On: Jul 14, 2024

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