Full 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.
Responsible for performing a wide variety of assignments in label copy control, sample management, documentation review, and other quality department functions.
May make detailed observations, analyze data, and interpret results.
Will maintain department equipment and inventory levels for controlled materials.
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.
Will perform troubleshooting, work independently, and make decisions based on general guidance and existing procedural requirements.
Will work in both Drug Delivery and Penicillin facilities as needed.
Regular overtime will be required to meet the production schedule.
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.
Performs product functional testing in support of equipment validations.
*** The candidate must not be allergic to penicillin or cephalosporin drugs ***
Associate’s Degree in related discipline or plus 0-3 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 in pharma manufacturing facilities.
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.
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
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.
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