Baxter International Inc.
Quality Lab Supervisor - Chemistry (3rd Shift)
Baxter International Inc., Round Lake, Illinois, United States, 60073
Quality Lab Supervisor - Chemistry (3rd Shift)
Base pay range: $80,000.00 – $110,000.00 per year
This is where
your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.
Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.
Here, you will find more than just a job—you will find purpose and pride.
Your role at Baxter This is a 3rd shift position.
4 days per week, 10 hours per shift (approximately 10:00 pm to 8:30 am).
What you'll be doing
Supervise safety measures of the lab. Assist lab personnel and improve their performance.
Ensure completion of all testing, including special project/protocol testing in a timely and appropriate manner.
Assist in implementing quality and regulatory requirements (e.g., FDA, GLP, QSR, cGMP, USP, and CDR rules and guidelines) and ensure compliance with testing SOPs and specifications.
Supervise the testing techniques and accuracy of all records and documentation performed in the lab.
Participate in proactive functions that impact production, increase efficiency, solve problems, generate cost savings, improve quality, and provide new product support.
Ensure employees are properly trained and audited. Make appropriate staffing decisions.
Prepare, review, and revise SOPs and specifications as required.
Ensure equipment maintenance and calibration; internal audits are performed on schedule.
What you'll bring
Bachelor’s Degree in Chemistry or a related biological science with analytical chemistry or laboratory coursework. Minimum 5 years experience in the healthcare industry.
Must know operating and troubleshooting procedures for lab equipment, and quality and regulatory requirements relevant to pharmaceutical and medical device manufacturing labs.
Must possess excellent supervisory and interpersonal skills and be able to communicate with subordinates, peers, and managers.
Must not be allergic to penicillin and cephalosporin drugs.
Must not be color blind.
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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This is where
your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.
Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.
Here, you will find more than just a job—you will find purpose and pride.
Your role at Baxter This is a 3rd shift position.
4 days per week, 10 hours per shift (approximately 10:00 pm to 8:30 am).
What you'll be doing
Supervise safety measures of the lab. Assist lab personnel and improve their performance.
Ensure completion of all testing, including special project/protocol testing in a timely and appropriate manner.
Assist in implementing quality and regulatory requirements (e.g., FDA, GLP, QSR, cGMP, USP, and CDR rules and guidelines) and ensure compliance with testing SOPs and specifications.
Supervise the testing techniques and accuracy of all records and documentation performed in the lab.
Participate in proactive functions that impact production, increase efficiency, solve problems, generate cost savings, improve quality, and provide new product support.
Ensure employees are properly trained and audited. Make appropriate staffing decisions.
Prepare, review, and revise SOPs and specifications as required.
Ensure equipment maintenance and calibration; internal audits are performed on schedule.
What you'll bring
Bachelor’s Degree in Chemistry or a related biological science with analytical chemistry or laboratory coursework. Minimum 5 years experience in the healthcare industry.
Must know operating and troubleshooting procedures for lab equipment, and quality and regulatory requirements relevant to pharmaceutical and medical device manufacturing labs.
Must possess excellent supervisory and interpersonal skills and be able to communicate with subordinates, peers, and managers.
Must not be allergic to penicillin and cephalosporin drugs.
Must not be color blind.
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.
#J-18808-Ljbffr