Quality Lab Supervisor
$80k - $110kBaxter Healthcare
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. 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 The Quality Lab Supervisor is responsible for overseeing the daily operations of the laboratory, ensuring the timely and accurate testing of raw materials, in-process samples, finished pharmaceutical products, and environmental monitoring samples. This role leads and develops laboratory personnel while maintaining compliance with FDA, cGMP, GLP, USP, and other regulatory requirements. The supervisor drives operational excellence by ensuring data integrity, laboratory safety, equipment reliability, staff training, and continuous improvement initiatives that support product quality, regulatory compliance, and manufacturing success What you'll be doing Provide support for daily operation of the laboratory and control of workflow. Implement testing standards and policies. Supervise safety measures of laboratory. Assist personnel and enhance 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, and USP rules and guidelines), and ensure compliance with testing SOPs and specifications. Monitor the testing techniques and accuracy of all records and documentation in the laboratory. Participate in pro-active functions that impact production, increase efficiency, solve problems, generate cost savings, improve quality, and provide new product support. Ensure employees are properly trained. Make appropriate staffing decisions. Prepare, review and revise, as required, SOPs and specifications. Ensure equipment maintenance and calibration, and internal audits are performed on schedule. Work Environment / Working Conditions This position requires work in a facility that manufactures penicillin products; therefore, candidates Must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. May be required to wear appropriate personal protective equipment (PPE). Exposure to pharmaceutical materials, chemicals, and manufacturing environments. What you'll bring Bachelor’s Degree in Chemistry, or related science with Chemistry coursework 4-6 years of experience in the healthcare industry. Must know operating and troubleshooting procedures for lab equipment, as well as, quality and regulatory requirements pertinent to pharmaceutical and medical device manufacturing labs. Must possess excellent supervisory and interpersonal skills and be able to communicate with subordinates, peers, and managers. We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $80,000 - $110,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, 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. US Benefits at Baxter (except for Puerto Rico) Baxter offers comprehensive compensation and benefits packages for eligible roles. medical and dental coverage that start on day one insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching Flexible Spending Accounts educational assistance programs time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave commuting benefits Employee Discount Program Employee Assistance Program (EAP) childcare benefits Join us and enjoy the competitive compensation and benefits we offer to our employees. 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. 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 let us know the nature of your request along with your contact information. #J-18808-Ljbffr
$80k - $110k
...exceptional results. Here, you will find more than just a job-you will find purpose and pride. Your role at Baxter The Quality Lab Supervisor is responsible for overseeing the daily operations of the laboratory, ensuring the timely and accurate testing of raw...SuggestedTemporary workWork visaFlexible hours$165k - $230k
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Corporate Process Quality Manager Spring Grove, IL | On-Site | Full-Time, Direct Hire | $100,000 to $120,000/yearAn employee-owned metals manufacturer in Spring Grove, Illinois is hiring a Corporate Process Quality Manager to lead the process side of its quality function...Full timeWork at officeNight shift$112.8k - $141k
...playing for Team Amcor, visit IYouTube Job Description The Plant Quality Manager is the quality advocate for the plant, providing... ...Manages and trains the activities of the Quality Team including the lab/quality technicians. Actively participates and leads teams in support...Full timeTemporary workRemote workWorldwideFlexible hours- A pharmaceutical company is seeking a Manager of Quality Systems responsible for providing quality assurance support across various manufacturing processes. The ideal candidate should have a Bachelor's degree in Life Sciences and a minimum of 8 years of quality experience...
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$112k - $154k
...just a job—you will find purpose and pride. Your Role at Baxter This is where your creativity addresses challenges As a Quality Manager at Baxter, you will lead the strategy and execution of training and qualification programs that support our RLDD...Temporary workWork visaFlexible hours- ...Skills and Requirements • Associate's degree preferred • 2+ years of relevant experience in customer service, complaint handling, quality assurance, product recalls, or documentation management • Experience in a regulated industry, preferably medical device or...Work at office
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