Quality Lab Technician I

1001 Baxter Healthcare Corporation; United States; On-site; USD 40,000 - 55,000; Full time

Benefits offered by this job

Medical and dental coverage starting—1

401(k) with company match

Employee Stock Purchase Plan

Job summary

Baxter is seeking a Quality Laboratory Technician – SDT to perform specialized destructive testing of sterile parenteral products, ensuring compliance with cGMP and quality systems. You will prepare samples, operate filtration and microscopy equipment, and document results.

This on-site role supports investigations, continuous improvement, and regulatory readiness in a controlled manufacturing environment.

Qualifications

• Knowledge of GDP and documentation practices.
• Familiarity with cGMP requirements and quality systems.
• Strong attention to detail and observational skills.
• Ability to identify small particulate defects and visual anomalies.
• Experience with microscopy and laboratory testing principles.

Responsibilities

• Perform SDT on IV solutions and sterile products using approved filtration methods.
• Prepare samples including product handling and filtration setup.
• Conduct membrane filtration testing in ISO 5 or similar environments.
• Inspect filtration membranes using microscopy and visual techniques.
• Detect, classify, document, and trend particulate observations.
• Maintain contamination-control through proper gowning and aseptic practices.
• Operate and maintain lab equipment (laminar flow hoods, filtration systems, microscopes).
• Accurately complete notebooks, worksheets, and electronic records.

Skills

GDP understanding

cGMP knowledge

Attention to detail

Microscopy basics

Documentation skills

Independent worker

Education

Associate degree in Biology, Chemistry, Microbiology, Engineering Technology, Quality Sciences, or related

High School Diploma or GED

Tools

Laminar flow hoods

Vacuum filtration systems

Stereomicroscopes

Digital imaging systems

Light measurement devices

Lab documentation systems

Job description

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.

Position Summary

The Quality Laboratory Technician – Supplemental Destructive Testing (SDT) is responsible for performing specialized destructive testing of sterile parenteral products to support particulate matter investigations, process monitoring, product quality surveillance, and continuous improvement initiatives. This position executes membrane filtration testing methods designed to detect and characterize visible particulate matter that may not be identified through conventional manual visual inspection processes. The technician performs sample preparation, filtration, microscopy, particulate characterization, laboratory documentation, equipment maintenance, and data collection activities in compliance with current Good Manufacturing Practices (cGMP), site procedures, and applicable pharmacopeial requirements. The role requires strict adherence to contamination-control practices while working in controlled laboratory environments.

Essential Duties and Responsibilities

• Perform Supplemental Destructive Testing (SDT) on IV solution and sterile parenteral products using approved filtration methods.
• Prepare samples for testing, including product handling, unit manipulation, and filtration system setup.
• Conduct membrane filtration testing within ISO 5 or similarly controlled environments.
• Inspect filtration membranes using visual inspection techniques and stereomicroscopy.
• Detect, classify, document, and trend particulate matter observations.
• Maintain contamination-control practices through proper gowning, aseptic behaviors, and environmental awareness.
• Perform clean blank filtrations and suitability checks prior to routine testing activities.
• Operate and maintain laboratory equipment including:
  • Laminar flow hoods
  • Vacuum filtration systems
  • Stereomicroscopes
  • Digital imaging systems
  • Light measurement devices
  • Sample preparation equipment
• Capture particulate images and assist with particle characterization investigations.
• Accurately complete laboratory notebooks, worksheets, logbooks, electronic systems, and testing records.
• Review testing results for completeness and compliance with procedural requirements.
• Support investigations involving visible particulate matter, foreign material, and product quality defects.
• Assist with laboratory studies, method improvements, equipment qualifications, and continuous improvement projects.
• Monitor laboratory cleanliness and maintain an organized, inspection‑ready work environment.
• Participate in laboratory training and qualification programs.
• Support internal audits, regulatory inspections, and customer audits as required.
• Identify and escape atypical results, procedural deviations, or equipment concerns to Quality leadership.

Required Qualifications

Education

• Associate degree in Biology, Chemistry, Microbiology, Engineering Technology, Quality Sciences, or a related scientific discipline preferred.
• High School Diploma or GED required.

Experience

• 1–3 years of experience in a laboratory, manufacturing, quality, or regulated environment preferred.
• Experience within pharmaceutical, medical device, biologics, or sterile manufacturing industries preferred.
• Experience performing visual inspection or particulate evaluation is desirable.

Knowledge, Skills, and Abilities

• Understanding of Good Documentation Practices (GDP).
• Knowledge of cGMP requirements and quality systems.
• Strong attention to detail and observational skills.
• Ability to identify small particulate defects and visual anomalies.
• Basic understanding of microscopy and laboratory testing principles.
• Ability to maintain focus during repetitive inspection and testing activities.
• Strong organizational and recordkeeping skills.
• Effective verbal and written communication abilities.
• Ability to work independently while following detailed procedures.
• Proficiency with Microsoft Office applications and laboratory documentation systems.

Physical Requirements

• Ability to sit or stand for extended periods.
• Ability to perform repetitive manual tasks requiring fine motor dexterity.
• Ability to visually inspect small particles and defects under varying magnification levels.
• Ability to wear required laboratory PPE for extended periods.
• Ability to lift up to 25 pounds occasionally.
• Correctable vision sufficient to perform microscopic and visual inspection activities.

Working Conditions

Controlled laboratory environment. Frequent work within ISO‑classified or cleanroom environments. Required use of laboratory and cleanroom personal protective equipment (PPE). Exposure to routine laboratory chemicals, cleaning agents, and sterile product materials. May require occasional off‑shift or weekend support for investigations and special studies.

Key Performance Indicators

• Testing accuracy and data integrity.
• Compliance with laboratory procedures and documentation requirements.
• Timely completion of assigned testing activities.
• Successful maintenance of qualification status.
• Investigation support responsiveness.
• Adherence to contamination‑control and safety requirements.
• Audit and inspection readiness.

US Benefits at Baxter (except for Puerto Rico)

• Medical and dental coverage that starts on day one.
• 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.
• 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.

Baxter 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.

Know Your Rights: Workplace Discrimination is Illegal. 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, let us know the nature of your request along with your contact information.

Company Culture

No matter your role at Baxter, your talent, skills, and time has a direct impact on people's lives. Since 1931, we have been at the forefront of innovation by bringing smarter, more personalized care to patients around the world. Now, we're more determined than ever to make a lasting impact as we are redefining healthcare delivery across the care journey. Our Mission to Save and Sustain Lives motivates us as we create a culture in which each of us can succeed. This is where you belong.

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 clear with our pay practices. The estimated base salary for this position is $40,000-$55,000 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 location, skills and expertise, experience, and other relevant factors.

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.