Quality Technician - 3rd Shift

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:

As a Quality Technician, you will play a pivotal role in ensuring that our manufacturing processes and methods meet the highest standards of quality and compliance. Your expertise will be essential in maintaining the integrity of our Quality System Regulation, ensuring that every product we produce is detailed and meets our outstanding standards.

Your team:

Baxter prioritizes the development of high-quality products that address patient needs. Our team is dedicated to putting patients first and takes pride in the value we deliver. Joining our multinational organization offers the opportunity to collaborate with diverse individuals, explore different areas of our portfolio, and receive ongoing support from our leadership team for personal growth.

What you'll be doing:

• Revise and approve all documentation related to areas of responsibility, including In Process Checker Charts, Product Retention Records, Control Charts, Mold Approvals, Batch Records, and more.

• Conduct routine manufacturing audits of machine parameters and set-ups to ensure compliance, as well as audits of the manufactured product.

• Perform routine audits of sampling techniques, testing skills, and all documentation performed by the TIQ's.

• Immediately notify and raise awareness to Quality Management about potential quality situations.

• Assist and coordinate protocols to ensure detailed execution.

• Provide training on Good Documentation Practices, SPC, Total Coordinated Quality, and other relevant areas.

• Support mold approval and mold start-up evaluations, if applicable.

• Gather, analyze, audit, and interpret data using SPC methods to predict trends and recommend process improvements that positively impact product quality, scrap reduction, DPM reduction, complaints reduction, and price of non-conformance reduction.

• Maintain, revise, and audit control charts, computing control chart limits as needed.

• Ensure that all machinery, equipment, tools, and supervisory materials align with Corporate, GMP, and other regulatory requirements.

• Publish monthly Quality Indicators, including DPM's and Pareto Analysis, within your areas of responsibility.

• Submit improvements and modifications to specifications and Standard Operating Procedures.

• Maintain timely communication and awareness of DPM and complaints trends with internal and external customers/suppliers, if applicable.

• Assist in the development and certification of TIQ's.

• Perform special projects related to your areas of responsibility.

• Document required information manually (e.g., checker charts) and electronically (e.g., POMs) to align with applicable procedures and specifications.

• Conduct EHS inspections to identify and mitigate safety hazards and environmental aspects, analyze EHS incidents, and take corrective actions.

• Observe data privacy policies at all times.

• Provide support for software application audits.

• Assist in the generation and investigation of non-conformities.

What you'll bring:

• Bachelor's degree in Science.

• At least two years of related job experience in the Medical Device Industry.

• Proficiency in Data Entry and Microsoft Office Software, with basic computer knowledge required.

• Experience with measurement instrumentation.

• Excellent interpersonal skills.

• Willingness to travel occasionally.

• Bilingual (English & Spanish).

Your ambition and proven record in quality assurance will help us maintain the remarkable standards that Baxter Healthcare Corporation is known for. Join us in our mission to save and sustain lives by ensuring the highest levels of quality in everything we do.

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.

EEO is the Law 
EEO is the law - Poster Supplement
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

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.