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Quality Control Analyst Hplc Jobs (NOW HIRING)

QC Analyst III

Piscataway, NJ ยท On-site

$24 - $32.25/hr

Description Position Summary The QC Analyst III will be responsible for analytical testing and data ... Demonstrated success working with techniques such as HPLC, SDS-PAGE, cell-based bioassays ...

QC Analyst II

Piscataway, NJ ยท On-site

$24 - $32.25/hr

Job Type Full-time Description Position Summary The QC Analyst II will be responsible for ... HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard ...

QC Analyst III

Piscataway, NJ ยท On-site

$24 - $32.25/hr

Job Type Full-time Description Position Summary The QC Analyst III will be responsible for ... HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard ...

QC Analyst II

Piscataway, NJ ยท On-site

$24 - $32.25/hr

Description Position Summary The QC Analyst II will be responsible for analytical testing and data ... Demonstrated success working with techniques such as HPLC, SDS-PAGE, cell-based bioassays ...

QC Analyst

Miami, FL ยท On-site

$23 - $30.75/hr

The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for ... HPLC, and measuring physical parameters (bulk and tapped densities, and particle size by sieve ...

QC Analyst

Miami, FL ยท On-site

$23 - $30.75/hr

The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for ... HPLC, and measuring physical parameters (bulk and tapped densities, and particle size by sieve ...

QC Analyst

Miami, FL ยท On-site

$23 - $30.75/hr

The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for ... HPLC, and measuring physical parameters (bulk and tapped densities, and particle size by sieve ...

QC Chemist

Cranbury, NJ ยท 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 ...

QC Chemist

Cranbury, NJ ยท 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 ...

Quality Control Analyst

Monroe, NC ยท 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 ...

QC Chemist

Cranbury, NJ ยท 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 ...

QC Chemist

Cranbury, NJ ยท 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 ...

QC Chemist

Cranbury, NJ ยท 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 ...

QC Chemist

Cranbury, NJ ยท 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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$16

$27

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

As of Jul 13, 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 are some common challenges faced by Quality Control Analysts working with 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.

What are the key skills and qualifications needed to thrive as a Quality Control Analyst HPLC, and why are they important?

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 Quality Control Analysts 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.
More about Quality Control Analyst Hplc jobs
What cities are hiring for Quality Control Analyst Hplc jobs? Cities with the most Quality Control Analyst Hplc job openings:
What states have the most Quality Control Analyst Hplc jobs? States with the most job openings for Quality Control Analyst Hplc jobs include:
Infographic showing various Quality Control Analyst Hplc job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 1% Internship, 86% Full Time, 6% Part Time, 1% Temporary, and 5% Contract. Highlights an 82% Physical, 5% Hybrid, and 13% Remote job distribution, with an average salary of $58,065 per year, or $27.9 per hour.
Quality Control Analyst III

Quality Control Analyst III

AllSTEM Connections

Rensselaer, NY โ€ข On-site

$91K/yr

Temporary

Medical, Dental, Vision, Retirement

Re-posted 25 days ago


Job description

Job Title: Senior Quality Control Analyst (Pharmaceuticals)
Role Overview
We are seeking a highly skilled Senior Quality Control Analyst to join our laboratory operations team. In this role, you will perform critical analytical testing for incoming raw materials, in-process samples, and final products to ensure the highest standards of safety and efficacy. You will be responsible for executing complex chromatography and wet chemistry assays while maintaining the validated state of the laboratory through instrument calibration and audit readiness. The ideal candidate is a disciplined scientist with deep experience in a GMP-regulated environment and a strong command of analytical troubleshooting.
Key Responsibilities
โ€ข Analytical Testing: Execute testing for raw materials, stability samples, and finished products using precision equipment, including balances, pH meters, UV/Vis spectrophotometers, and TOC analyzers.
โ€ข Advanced Chromatography: Perform high-level chromatography (HPLC and GC) following extensive site-specific qualification and training.
โ€ข Laboratory Governance: Oversee general laboratory maintenance, housekeeping, and instrument calibration routines to ensure constant audit readiness.
โ€ข Data Review & Reporting: Assist management in the review of QC data, providing summaries and technical reports that interpret complex analytical results.
โ€ข Investigations & Compliance: Support QC Management in conducting Out-of-Specification (OOS) investigations, deviations, and CAPAs using data-driven fact-finding.
โ€ข Logistics & Coordination: Manage sample receipt, processing, and distribution for both internal and external laboratory testing, ensuring accurate tracking and result closure.
โ€ข Environmental Monitoring: Regularly perform water sample collection and testing in accordance with site environmental protocols.
Qualifications & Requirements
โ€ข Education: Bachelor's Degree in Chemistry or a closely related scientific field is required.
โ€ข Experience: * Minimum of 5+ years of professional experience in a Pharmaceutical Quality Control environment.
โ€ข Proven expertise in testing APIs (Active Pharmaceutical Ingredients) and/or Finished Dosages.
โ€ข Technical Mastery:
โ€ข Must have working knowledge of HPLC and GC systems.
โ€ข Strong understanding of FDA GMPs (21 CFR 211, 820, and/or 600); ISO 9001/13485 is a plus.
โ€ข Proficiency in advanced mathematical concepts (ANOVA, correlation techniques, sampling theory) and statistical analysis.
โ€ข Physical Requirements: Ability to stand/walk for extended periods, lift up to 50 lbs, and work in a lab environment requiring manual dexterity and close vision focus. Equal Opportunity Employer / Disabled / Protected Veterans
The Know Your Rights poster is available here:
https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12.pdf
The pay transparency policy is available here:
https://www.dol.gov/sites/dolgov/files/ofccp/pdf/pay-transp_%20English_formattedESQA508c.pdf
For temporary assignments lasting 13 weeks or longer, AllSTEM Connections is pleased to offer major medical, dental, vision, 401k and any statutory sick pay where required.
We are committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation for any part of the employment process, please contact your staffing representative who will reach out to our HR team.
AllSTEM Connections participates in the E-Verify program in certain locations as required by law. Learn more about the E-Verify program.
https://e-verify.uscis.gov/web/media/resourcesContents/E-Verify_Participation_Poster_ES.pdf
We also consider for employment qualified applicants regardless of criminal histories, consistent with legal requirements, including, if applicable, the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records, including, if applicable, the San Francisco Fair Chance Ordinance. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
Additional Skills
(none specified)
AllSTEM Representative Contact Info
Account Executive:
Nichols
Branch Phone:
(909) 244-1777
Location:
Ontario, CA