New · posted Nov 6
Baxter · Pharmaceuticals
Quality Lab Technician I
- Marion, NC
- On-site
- Full-time
- Associate & Specialist
The role
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.
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.
What you need
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.
What you'll do
- 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 escalate atypical results, procedural deviations, or equipment concerns to Quality leadership.
Pay
$40,000 – $55,000 a year
Employer providedKey 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.
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 upon location, skills and expertise, experience, and other relevant factors. 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.
This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the 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. We also offer Flexible Spending Accounts, educational assistance programs, and 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. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter
Where you'll work
Marion, NCOn-siteOpen in Maps (opens in a new tab)
More jobs in Marion, NCWorking 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.
Equal opportunity, accessibility and legal noticesBaxter's statements, word for word
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 link 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 Recruitment Fraud Notice.
Job intelligence
The context around this role
Live data · November 6, 2026
Salary intelligence
How the pay compares
This role's midpoint is 35% below the US median for Quality Control roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US84 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $40,000 | — | $55,000 |
| All US (middle half) | $61,500 | $73,500 | $90,125 |
This role: Baxter's own published range. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, November 6, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 250 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Baxter's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 44 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods18
- GMP and compliance10
- Documentation and SOPs6
- Investigations and CAPA4
- Collaboration and leadership4
- Quality systems and risk3
- Data and digital systems2
- Validation and qualification1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Control work in pharmaceuticals, led by the two this posting names, each linked to the agency or standards body that publishes it.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticalsNamed in the posting
- EUEU Good Distribution Practice(official source, opens in a new tab)Guidelines on good distribution practice of medicinal products for human useNamed in the posting
- USPUSP–NF(official source, opens in a new tab)US Pharmacopeia general chapters and monographs, such as <61> bioburden, <85> endotoxin, <1225> validation
- FDAFDA OOS guidance(official source, opens in a new tab)Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and Answers
- FDAFDA aseptic processing guidance(official source, opens in a new tab)Sterile Drug Products Produced by Aseptic Processing: Current Good Manufacturing Practice
- ISOISO 14644-1(official source, opens in a new tab)Cleanroom air cleanliness classification by particle concentration
- FDAFDA Investigations Operations Manual(official source, opens in a new tab)How FDA investigators plan and conduct inspections
- ISOISO 19011(official source, opens in a new tab)Guidelines for auditing management systems
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- ICHICH Q2(R2) and Q14(official source, opens in a new tab)Validation and development of analytical procedures
- FDAFDA analytical procedures guidance(official source, opens in a new tab)Analytical Procedures and Methods Validation for Drugs and Biologics
- ICHICH Q1 stability testing(official source, opens in a new tab)Stability testing of drug substances and drug products
- EDQMEuropean Pharmacopoeia(official source, opens in a new tab)The Ph. Eur. quality standards for medicines in Europe, published by the EDQM
- ICHICH Q3 impurities(official source, opens in a new tab)Impurities in drug substances and products, residual solvents and elemental impurities
- EUEU GMP (EudraLex Volume 4)(official source, opens in a new tab)The EU's good manufacturing practice rules, including Annex 1 sterile and Annex 15 validation
Company hiring pulse
Baxter on Regulatory Jobs
- 47
- Open roles
- 47
- Distinct roles
- 11
- Locations
By discipline
- Quality43 90%
- Regulatory5 10%
By level
- Associate & Specialist21 44%
- Senior & Principal11 23%
- Manager8 17%
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Quality Lab Technician I at Baxter
Open until filled. $40K–$55K a year, employer provided.