Baxter International Inc.
Quality Lab Supervisor - Particulate Matter,
Baxter International Inc., Marion, North Carolina, United States, 28752
Quality Lab Supervisor - Particulate Matter
Join to apply for the
Quality Lab Supervisor - Particulate Matter
role at
Baxter International Inc.
6 days ago Be among the first 25 applicants
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 where your creativity addresses challenges. You are creative, thorough, and a heads‑down do‑er. You embrace a challenge and truly apply the collaborative powers of your team to produce great results. As a
Quality Lab Supervisor – Particulate Matter , you navigate necessary internal processes to facilitate a product you deeply believe in. You absorb and act on complex procedures and data and train your team or peers if needed. You take pride in getting things done quickly without sacrificing safety or quality.
Your team is integral to Baxter’s quality function, which values both teamwork and independent work. You will be responsible for direct supervision of Quality Technicians performing finished product testing of solutions in accordance with USP, reviewing test results within POMS or BaxLIMS, coordinating release of test results within specified timeframes, and ensuring all tasks required are completed within the assigned shift. You will complete follow‑up actions for any nonconformances and maintain training qualification on test methods.
What We Offer From Day One
Shift flexibility to trade shifts and leverage overtime opportunities
Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401(k) match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement
What You’ll Be Doing
Oversee daily shift operations of the QC PM Lab, including scheduling and resource management
Manage and lead a team of quality control technicians responsible for executing tests for particulate matter through filtration and visual inspection
Assign tasks, set priorities, and ensure effective performance and development of team members
Conduct regular training for staff to ensure work is performed accurately and efficiently, following established protocols and standards
Conduct ACE Check‑ins with staff and additional communications as needed
Troubleshoot and resolve any issues that arise during testing or lab equipment
Perform follow‑up for out‑of‑limit results including PM characterization, issuance of nonconformance, laboratory investigation, and coordinate follow‑up testing as required by procedure
Maintain and update standard operating procedures (SOPs) to reflect current practice and regulatory changes
Review results and address documentation errors in accordance with procedural requirements
Ensure that all data is documented properly, and reports are generated and reviewed in a timely manner
Perform trending of testing including efficiency metrics and results
Implement and enforce safety protocols and practices within the laboratory
What You’ll Bring
Bachelor’s degree in science (e.g., Engineering, Chemistry, Life Science, Biology)
2+ years of experience with aseptic technique in laboratory or manufacturing environments
Strong understanding of quality principles and Good Manufacturing Practice, including Good Documentation Practice
Excellent attention to detail and ability to focus on repetitive tasks
Computer skills including knowledge of Microsoft Office applications (Word, Excel)
Good interpersonal skills and ability to work effectively in a team‑based environment in small spaces
Able to manage multiple tasks/priorities in a timely manner
Able to work independently and manage time to complete assigned tasks
Schedule flexibility on occasion to ensure testing is performed in defined timeframes
Ability to perform testing using aseptic techniques, often requiring manual dexterity
Ability to lift 10–20 pounds routinely
Ability to pass inspector qualification requirements for visual inspection
Working Conditions
Laboratory environment, manufacturing environment
May require standing/walking for extended periods of time throughout the shift
Personal Protective Equipment (PPE) will be provided and must be worn as required in specified areas. PPE may include ear plugs, lab coats, safety glasses, hairnets, and shoe covers.
Other Duties As Assigned This job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Overtime is worked as required.
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. Individual pay is based on 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, please speak to the recruiter if you decide to apply and are selected for an interview.
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.
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.
Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.
Seniority level Mid-Senior level
Employment type Full-time
Job function Quality Assurance
Industries Medical Equipment Manufacturing
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Quality Lab Supervisor - Particulate Matter
role at
Baxter International Inc.
6 days ago Be among the first 25 applicants
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 where your creativity addresses challenges. You are creative, thorough, and a heads‑down do‑er. You embrace a challenge and truly apply the collaborative powers of your team to produce great results. As a
Quality Lab Supervisor – Particulate Matter , you navigate necessary internal processes to facilitate a product you deeply believe in. You absorb and act on complex procedures and data and train your team or peers if needed. You take pride in getting things done quickly without sacrificing safety or quality.
Your team is integral to Baxter’s quality function, which values both teamwork and independent work. You will be responsible for direct supervision of Quality Technicians performing finished product testing of solutions in accordance with USP, reviewing test results within POMS or BaxLIMS, coordinating release of test results within specified timeframes, and ensuring all tasks required are completed within the assigned shift. You will complete follow‑up actions for any nonconformances and maintain training qualification on test methods.
What We Offer From Day One
Shift flexibility to trade shifts and leverage overtime opportunities
Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401(k) match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement
What You’ll Be Doing
Oversee daily shift operations of the QC PM Lab, including scheduling and resource management
Manage and lead a team of quality control technicians responsible for executing tests for particulate matter through filtration and visual inspection
Assign tasks, set priorities, and ensure effective performance and development of team members
Conduct regular training for staff to ensure work is performed accurately and efficiently, following established protocols and standards
Conduct ACE Check‑ins with staff and additional communications as needed
Troubleshoot and resolve any issues that arise during testing or lab equipment
Perform follow‑up for out‑of‑limit results including PM characterization, issuance of nonconformance, laboratory investigation, and coordinate follow‑up testing as required by procedure
Maintain and update standard operating procedures (SOPs) to reflect current practice and regulatory changes
Review results and address documentation errors in accordance with procedural requirements
Ensure that all data is documented properly, and reports are generated and reviewed in a timely manner
Perform trending of testing including efficiency metrics and results
Implement and enforce safety protocols and practices within the laboratory
What You’ll Bring
Bachelor’s degree in science (e.g., Engineering, Chemistry, Life Science, Biology)
2+ years of experience with aseptic technique in laboratory or manufacturing environments
Strong understanding of quality principles and Good Manufacturing Practice, including Good Documentation Practice
Excellent attention to detail and ability to focus on repetitive tasks
Computer skills including knowledge of Microsoft Office applications (Word, Excel)
Good interpersonal skills and ability to work effectively in a team‑based environment in small spaces
Able to manage multiple tasks/priorities in a timely manner
Able to work independently and manage time to complete assigned tasks
Schedule flexibility on occasion to ensure testing is performed in defined timeframes
Ability to perform testing using aseptic techniques, often requiring manual dexterity
Ability to lift 10–20 pounds routinely
Ability to pass inspector qualification requirements for visual inspection
Working Conditions
Laboratory environment, manufacturing environment
May require standing/walking for extended periods of time throughout the shift
Personal Protective Equipment (PPE) will be provided and must be worn as required in specified areas. PPE may include ear plugs, lab coats, safety glasses, hairnets, and shoe covers.
Other Duties As Assigned This job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Overtime is worked as required.
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. Individual pay is based on 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, please speak to the recruiter if you decide to apply and are selected for an interview.
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.
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.
Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.
Seniority level Mid-Senior level
Employment type Full-time
Job function Quality Assurance
Industries Medical Equipment Manufacturing
#J-18808-Ljbffr