Quality Tech, Line Operations - 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

**This role is supporting 3rd shift: 11pm-7am**

The Quality Technician is responsible for performing a wide variety of assignments in label copy control, sample management, documentation review, and other quality department functions. This is a supporting role specifically for the manufacturing lines.

What you'll be doing

• Makes detailed observations, analyze data, and interpret results.
• Maintains department equipment and inventory levels for controlled materials.
• Interacts 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.
• Performs troubleshooting, works independently, and makes decisions based on general guidance and existing procedural requirements.
• Performs in process and/or final review of batch and/or critical systems documentation and determines acceptability by using standard operating procedures. Ensures presence and acceptability of all required documentation prior to the release of the product and/or system.
• Responsible for batch and/or critical systems review. Achieves and maintains batch or systems release qualification within assigned production cell.
• Reviews documentation such as protocols, CWRs, qualifications, etc. as assigned.
• Enters data into the Batch Release System. Generates reports from Trackwise 8.
• Performs product functional testing in support of equipment validations.

What you'll bring

• Associate degree in related discipline or 6 months or more years related experience.
• Basic science, math, and computer skills (including Microsoft Word and Excel) are required.
• Good writing and verbal communication skills, and problem-solving skills are required.
• Ability to work in a team environment and make independent decisions based on procedural and regulatory requirements
• It is desirable for the candidate to have experience with the requirements of current Good Manufacturing & Documentation Practices inpharma manufacturingfacilities.
• The candidate must be able to work flexible hours in a dynamic environment with minimal direct supervision.
• The ability to work some Saturdays is required.
• Will work in both Drug Delivery and Penicillin facilities as needed.
• Overtime may be required to meet the production schedule.
• *** Thecandidate must not be allergic to penicillin or cephalosporin drugs ***

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

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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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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