Baxter
Quality Lab Associate II – Endotoxin (7pm-7am)
Baxter, Marion, North Carolina, United States, 28752
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 creativity addresses challengesConduct microbiological analysis on raw materials, solution, and water samples following approved Standard Operating Procedures in an accurate and timely manner.Within Quality, every role makes a difference. Products that Baxter makes are shipped worldwide for patients in need. Whether it’s building a new process from scratch or facing a never-before-seen production hurdle, individuals within Quality are given the trust and opportunity to bring creativity to the table. Regardless of your specific role with a product, it is sure to touch a portion of our global operation.The mission of Baxter is to save and sustain lives. This mission is embedded into everything we do. This means if there is a decision to be made where quantity and quality are at odds, we will always choose quality. Our patients come first, always.What we offer from Day One
Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401K match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement
What you’ll be doing
Prepare samples and perform endotoxin testing on raw materials, solution, and water for bioburden
Perform particulate matter testing on solution
Perform daily pH meter, balance, and pipette verification
Perform daily Honeywell automated temperature checks and manual temperature monitoring
Perform peptidoglycan and gel clot testing as needed
Manage reagent inventory
Generate monthly trend reports
Calibration of micro-pipettes, analytical balance, water bath, dry heat bath, depyrogenation ovens, light obscuration particle counters and spectrophotometer
Responsible for daily lab upkeep including cleaning, glassware washing and depyrogenation, supply replenishment, syringe and endotoxin prep
Assist in method validation and protocol testing as needed
Sustain a clean and safe work environment utilizing 6S principles
Operate laboratory instrumentation and equipment such as laminar flow hoods, micro-pipettors, pH meters, analytical balances, and instruments used to perform particulate matter and endotoxin testing
Write and revise Standard Operating Procedures and review job‑related technical documents
Perform laboratory and manufacturing audits as required
Train others to perform microbiological testing/tasks
Serve as mentor to Quality Lab Associate I (QLA I) positions
Serve as a back‑up to Quality Lab Associate III (QLA III) in their absence
Write exceptions, nonconformance reports (NCRs) and CAPAs as needed utilizing TrackWise
What you’ll bring
B.S. degree in Microbiology, Biology, or related science
Minimum 2 years’ experience or Master’s Degree in biological sciences with hands‑on experience, preferably in the pharmaceutical or medical device industry
Computer literate/knowledge of Microsoft office applications (Word, Excel)
Proficient in quality based computer systems such as LIMS, POMS, Endoscan‑V software, Sampler Sight Pharma, and AS400
Attention to detail and ability to prioritize multiple tasks
Proficient in the operation of laboratory instrumentation and equipment such as laminar flow hoods, micro‑pipettors, pH meters, analytical balances, and instruments used to perform particulate matter and endotoxin testing
Good documentation skills and knowledge of GDPs (Good Documentation Practices)
Knowledge of aseptic sampling and testing techniques and microbiological testing according to FDA, cGMP, GLPs and USP testing methodology
Must be able to communicate effectively with supervisors and peers
Must be experienced in executing general microbiology procedures
Must be able to stand for extended periods
Must be able to lift 50 lbs
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 $64,000 – $88,000 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 on 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, please speak to the recruiter if you decide to apply and are selected for an interview.
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 requiredApplicants 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#LI-EB1US
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 click on the here and 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 .
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Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401K match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement
What you’ll be doing
Prepare samples and perform endotoxin testing on raw materials, solution, and water for bioburden
Perform particulate matter testing on solution
Perform daily pH meter, balance, and pipette verification
Perform daily Honeywell automated temperature checks and manual temperature monitoring
Perform peptidoglycan and gel clot testing as needed
Manage reagent inventory
Generate monthly trend reports
Calibration of micro-pipettes, analytical balance, water bath, dry heat bath, depyrogenation ovens, light obscuration particle counters and spectrophotometer
Responsible for daily lab upkeep including cleaning, glassware washing and depyrogenation, supply replenishment, syringe and endotoxin prep
Assist in method validation and protocol testing as needed
Sustain a clean and safe work environment utilizing 6S principles
Operate laboratory instrumentation and equipment such as laminar flow hoods, micro-pipettors, pH meters, analytical balances, and instruments used to perform particulate matter and endotoxin testing
Write and revise Standard Operating Procedures and review job‑related technical documents
Perform laboratory and manufacturing audits as required
Train others to perform microbiological testing/tasks
Serve as mentor to Quality Lab Associate I (QLA I) positions
Serve as a back‑up to Quality Lab Associate III (QLA III) in their absence
Write exceptions, nonconformance reports (NCRs) and CAPAs as needed utilizing TrackWise
What you’ll bring
B.S. degree in Microbiology, Biology, or related science
Minimum 2 years’ experience or Master’s Degree in biological sciences with hands‑on experience, preferably in the pharmaceutical or medical device industry
Computer literate/knowledge of Microsoft office applications (Word, Excel)
Proficient in quality based computer systems such as LIMS, POMS, Endoscan‑V software, Sampler Sight Pharma, and AS400
Attention to detail and ability to prioritize multiple tasks
Proficient in the operation of laboratory instrumentation and equipment such as laminar flow hoods, micro‑pipettors, pH meters, analytical balances, and instruments used to perform particulate matter and endotoxin testing
Good documentation skills and knowledge of GDPs (Good Documentation Practices)
Knowledge of aseptic sampling and testing techniques and microbiological testing according to FDA, cGMP, GLPs and USP testing methodology
Must be able to communicate effectively with supervisors and peers
Must be experienced in executing general microbiology procedures
Must be able to stand for extended periods
Must be able to lift 50 lbs
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 $64,000 – $88,000 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 on 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, please speak to the recruiter if you decide to apply and are selected for an interview.
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 requiredApplicants 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#LI-EB1US
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 click on the here and 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 .
#J-18808-Ljbffr