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Quality Control Analyst Hplc Jobs (NOW HIRING)

Lonza

QC Analyst II-Chromatography

Portsmouth, NH

$24.50 - $32.75/hr

Job Title: QC Analyst II-Chromatography Location: Portsmouth, NH, (On-site) As a QC Analyst II, ... This role is ideal for someone with hands-on HPLC experience who enjoys problem-solving, continuous ...

Lonza

QC Analyst II-Chromatography

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Job Title: QC Analyst II-Chromatography Location: Portsmouth, NH, (On-site) As a QC Analyst II, ... This role is ideal for someone with hands-on HPLC experience who enjoys problem-solving, continuous ...

Labor Solutions, LLC

Senior QC Analyst

Wheeling, IL · On-site

$25 - $33/hr

Senior QC Analyst Hourly * Part-Time or Full-Time * Flexible Schedule A premier Midwest ... The chemist will perform sample intake and preparation, run analyses on our Agilent HPLC and GC-MS ...

Glenmark Pharmaceuticals

Quality Control Analyst

Monroe, NC · On-site

$22.25 - $30/hr

Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in ... HPLC, UV-Vis and FTIR. Knowledge and Skills : Knowledge of cGMP, Validations and Qualifications ...

Catalent, Inc.

Quality Control Analyst

Winchester, KY · On-site

$20.75 - $27.75/hr

Quality Control Analyst Position Summary * Typical working hours are on E shift (6 AM- 6 PM ... FTIR, HPLC, and GC, etc. * Maintain accurate written records of all analysis performed.

Catalent, Inc.

Quality Control Analyst

Winchester, KY · On-site

$20.75 - $27.75/hr

Quality Control Analyst Position Summary * Typical working hours are Monday-Friday 3 PM - 11:30 PM ... FTIR, HPLC, and GC, etc. * Maintain accurate written records of all analysis performed.

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... HPLC/UPLC analysis. Key Responsibilities * Perform batch release and stability testing for ...

Catalent, Inc.

Quality Control Analyst

Winchester, KY · On-site

$20.75 - $27.75/hr

Quality Control Analyst Position Summary * Typical working hours are Monday-Friday 11 PM - 7:30 AM ... FTIR, HPLC, and GC, etc. * Maintain accurate written records of all analysis performed.

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... HPLC/UPLC analysis. Key Responsibilities * Perform batch release and stability testing for ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... HPLC/UPLC analysis. Key Responsibilities * Perform batch release and stability testing for ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... HPLC/UPLC analysis. Key Responsibilities * Perform batch release and stability testing for ...

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Quality Control Analyst Hplc information

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How much do quality control analyst hplc jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for quality control analyst hplc in the United States is $27.92, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $31.01 per hour, depending on experience, location, and employer.

What is a quality control analyst HPLC?

Quality Control Analysts HPLC are laboratory professionals who use High-Performance Liquid Chromatography (HPLC) to analyze and verify the quality, purity, and composition of pharmaceutical products, chemicals, or other materials. Their primary role is to ensure products meet regulatory standards and specifications by running precise analytical tests. They maintain and calibrate HPLC instruments, prepare samples, interpret data, and document results to support product release and compliance. This position is critical in industries such as pharmaceuticals, biotechnology, and food safety.

What skills and qualifications are needed to be a quality control analyst HPLC?

To thrive as a Quality Control Analyst HPLC, you need a solid background in chemistry or pharmaceutical sciences, often supported by a relevant degree and experience with laboratory testing. Proficiency in operating and troubleshooting High Performance Liquid Chromatography (HPLC) systems, as well as familiarity with laboratory information management systems (LIMS) and relevant regulatory standards (such as GMP), is essential. Attention to detail, strong problem-solving abilities, and effective communication skills distinguish top performers in this role. These skills ensure accurate results, regulatory compliance, and efficient collaboration, which are critical for maintaining product quality and safety.

What are common challenges faced by quality control analysts HPLC, and how can they be addressed?

Quality Control Analysts using HPLC often encounter challenges such as instrument calibration issues, column degradation, and sample contamination. Staying proactive with routine maintenance, adhering strictly to SOPs, and troubleshooting inconsistencies in chromatograms are essential for ensuring data accuracy. Collaboration with colleagues in method development and validation teams can also help address complex analytical issues and enhance overall lab performance. Continuous learning and hands-on experience with various HPLC systems further equip analysts to manage these challenges efficiently.

What is the difference between Quality Control Analyst Hplc vs Quality Control Analyst Uplc?

AspectQuality Control Analyst HplcQuality Control Analyst Uplc
CertificationsOften requires HPLC certification or trainingMay require UPLC-specific training or certifications
Work EnvironmentLaboratories using HPLC equipment for analysisLaboratories utilizing UPLC systems for faster, high-resolution testing
Industry UsageCommon in pharmaceuticals, biotech, and chemical industriesUsed in similar industries, especially where high-throughput analysis is needed
Job FocusAnalyzing samples with HPLC for purity, potency, and stabilityPerforming similar analyses with UPLC for quicker results

Both roles involve analytical testing in laboratory settings, with UPLC offering faster and higher-resolution analysis compared to HPLC. The choice depends on the company's equipment and testing needs, but both require similar certifications and industry experience.

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Quality Control Analyst Hplc jobs near you
Infographic showing various Quality Control Analyst Hplc job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $58,065 per year, or $27.9 per hour.

QC Analyst II-Chromatography

Lonza Group Ltd.

Portsmouth, NH • On-site

$70 - $90/hr

Other

Medical, Dental, Vision

This job post has expired today. Applications are no longer accepted.

Job description

Job Title: QC Analyst II-ChromatographyLocation: Portsmouth, NH (On-site)

As a QC Analyst II, Chromatography, you will play an important role in supporting the release of in-process and final product drug lots through analytical testing and quality control activities. Working within a GMP-regulated laboratory, you will perform chromatography-based assays, troubleshoot laboratory equipment, review data, and support customer stability studies. This role is ideal for someone with hands‑on HPLC experience who enjoys problem-solving, continuous improvement, and maintaining high-quality standards.

What you will get:
  • An agile career and dynamic working culture
  • An inclusive and ethical workplace
  • Compensation programs that recognize performance
  • Medical, dental, and vision insurance
  • Opportunities to grow and develop your career
  • A collaborative and supportive team environment
  • The opportunity to support the delivery of life‑changing therapies
What you will do:
  • Perform chromatography testing to support in-process, final product, and stability testing activities
  • Execute analytical assays including Protein A, SEC, CEX, HIC, pH, conductivity, and reagent preparation
  • Troubleshoot laboratory instrumentation, including HPLC systems, pH meters, conductivity meters, and pipettes
  • Review analytical data to ensure accuracy, compliance, and timely delivery of results
  • Train and mentor analysts on laboratory methods and procedures
  • Support campaign readiness by ensuring reagents, materials, and equipment are available and maintained
  • Review and update laboratory documentation, procedures, and quality records
  • Initiate and support quality investigations, equipment tag‑outs, and related quality system activities
  • Participate in audit readiness activities and help maintain an inspection‑ready laboratory environment
  • Apply data integrity principles and GMP requirements in all aspects of laboratory work
What we are looking for:
  • Associate’s degree in Chemistry, Biochemistry, or a related science field
  • Limited experience in a laboratory or regulated environment preferred
  • Basic understanding of laboratory with chromatography and HPLC systems
  • Strong attention to detail and ability to follow instructions
  • Good written and verbal communication skills
  • Ability to prioritize tasks and work as part of a team
  • Experience training or mentoring others is a plus
About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table.

At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law.

If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

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