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Job Details

Quality Lab Associate

Company name

Cleveland, MS
13 hit(s)  


Quality Lab Associate','180007MS','!*!

Perform chemical and physical analysis on medical products through all stages of the manufacturing process from incoming raw materials through to product release.  Areas include raw materials, initial, in-process, finished products, stability program, protocol support, instrumental analysis and instrument calibration/qualifications.

Adhere to regulatory and procedural requirements that govern the operations and products.

Perform chemical quantitative and qualitative analysis on intravenous solutions, sets, devices, raw materials, and plant water (distilled and non-distilled) utilizing 'wet' chemistry techniques and instrument analysis.

Use laboratory instruments and computer systems to collect and record data.

Perform analysis requiring precise analytical skills and understanding of chemistry principles.

Perform deviations investigations, problem solve, and write exception documents.

Prepare and perform protocols.

Ensure regulatory compliance.

Complete and review documentation.

Complete all testing, including special projects/protocol testing in a timely and appropriate manner.

Perform all other duties and responsibilities as determined by supervision/management.','!*!

Strong computer competency required.

Ability to work in a team environment and independently.

Demonstration of good organization and time management skills.

Good oral and written communication skills, including technical terms.

Ability to handle multiple priorities.

General knowledge of environmental health and safety regulations applicable to plant and chemistry lab department required.

Must be able to work off-shift hours and some weekends as needed in order to support manufacturing.

Bachelors degree in Chemistry or Biological Science with Analytical Chemistry or Laboratory coursework and 0-2 years experience at equivalent level of responsibility.

Experience in FDA regulated industry a plus.

Experience with instrument analysis preferred.


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 LawEEO is the law - Poster SupplementPay Transparency Policy

Reasonable AccommodationsBaxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to and let us know the nature of your request along with your contact information.','Quality','United States of America-Mississippi-Cleveland','','Global Quality - US/Canada Operations','Full-time','Quality Lab Associate

Company info

Website :

Company Profile
Baxter International Inc. (NYSE:BAX), through its subsidiaries, develops, manufactures and markets products that save and sustain the lives of people with hemophilia, immune disorders, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create products that advance patient care worldwide. Baxter had 2013 sales of $15.3 billion and has approximately 61,500 employees.

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