ZipRecruiter

Log In

1

Quality Control Analyst Hplc Jobs (NOW HIRING)

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 Holdings, LLC

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 3 PM - 11:30 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.

AskBio

Quality Control Analyst II

Durham, NC · On-site

$23.25 - $31.25/hr

The Quality Control Analyst II will be responsible for performing routine testing on analytical ... Experience with cell-based assays, PCR testing, and/or HPLC testing * Experience working within a ...

AskBio

Quality Control Analyst

Durham, NC · On-site

$23.25 - $31.25/hr

The Quality Control Analyst I will be responsible for performing routine GMP testing on analytical ... HPLC techniques * Prepares laboratory solutions, maintains cell lines, maintain inventory of ...

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.

AskBio

Quality Control Analyst II

Durham, NC · On-site

$23.25 - $31.25/hr

The Quality Control Analyst II will be responsible for performing routine testing on analytical ... Experience with cell-based assays, PCR testing, and/or HPLC testing * Experience working within a ...

AskBio

Quality Control Analyst

Durham, NC · On-site

$23.25 - $31.25/hr

The Quality Control Analyst I will be responsible for performing routine GMP testing on analytical ... HPLC techniques * Prepares laboratory solutions, maintains cell lines, maintain inventory of ...

Astrix Inc

Quality Control Analyst I/III

Santa Rosa, CA · On-site

$39.90 - $60.10/hr

Perform complex analytical testing including HPLC, ELISA, and other advanced techniques with ... Qualifications QC Analyst I * Bachelor's degree in Chemistry, Biology, Biochemistry, or a related ...

KBI Biopharma, Inc.

QC Analyst II

Durham, NC

$23.25 - $31.25/hr

In-process and release testing as assigned; techniques include (but not limited to) HPLC, SDS-CGE ... Senior QC Analyst requires Bachelor' degree as described and 4+ years' experience or Master ...

Astrix Inc

QC Analyst III (Pharma)

Ventura, CA · On-site

$58 - $60/hr

Job type: 6-month contract (possibility of extension or conversion) Job Summary The QC Analyst III ... Perform complex analytical testing and data evaluation using techniques such as HPLC, ELISA, and ...

KBI Biopharma, Inc.

QC Analyst II

Durham, NC · On-site

$23.25 - $31.25/hr

In-process and release testing as assigned; techniques include (but not limited to) HPLC, SDS-CGE ... Senior QC Analyst requires Bachelor' degree as described and 4+ years' experience or Master ...

next page

Showing results 1-20

All JobsQuality Control Analyst Hplc Jobs

Quality Control Analyst Hplc information

See salary details

$16

$27

$41

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

As of Jun 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 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:
What job categories do people searching Quality Control Analyst Hplc jobs look for? The top searched job categories for Quality Control Analyst Hplc jobs are:
Quality Control Analyst Hplc jobs near you
QC Chemist

QC Chemist

System One

Cranbury, NJ • On-site

$36 - $40/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 5 days ago

Job description

Job Title: QC Chemist (cGMP / HPLC / Solid Dose) Location: Cranbury, NJ (Onsite) Type: Contract-to-Hire Schedule: 40 hrs/week Shift: M-F 8am-5pm Pay: $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release, stability testing, and analytical testing in a cGMP pharmaceutical manufacturing environment. Ideal candidates will have strong experience with solid oral dosage forms (tablets/capsules) and hands-on HPLC/UPLC analysis. Key Responsibilities

  • Perform batch release and stability testing for pharmaceutical products
  • Conduct assay, dissolution, impurity, and related substances testing
  • Operate, calibrate, and troubleshoot HPLC / UPLC systems
  • Maintain GMP documentation and ensure audit readiness (ALCOA+)
  • Investigate OOS / OOT results and support CAPA activities
  • Manage stability programs, sample pulls, and trending analysis
  • Collaborate with QA and Manufacturing to meet production timelines

Requirements

  • 6–8+ years of pharmaceutical QC experience (cGMP REQUIRED)
  • Strong background in solid oral dosage (tablets, capsules)
  • Recent hands-on experience with HPLC / UPLC (REQUIRED)
  • Experience with assay, dissolution, impurities, and stability testing
  • Working knowledge of FDA, GMP, ICH guidelines
  • Experience with Empower, LIMS, or similar systems
  • Strong documentation, data integrity (ALCOA+), and troubleshooting skills
  • Ability to work independently and in a fast-paced manufacturing setting

Keyskills QC Chemist, Quality Control Analyst, cGMP, GMP, Pharmaceutical, Solid Dose, Solid Oral Dosage, Tablets, Capsules, HPLC, UPLC, Dissolution, Assay, Impurities, Stability Testing, Batch Release, OOS, OOT, CAPA, FDA, ICH, Empower, LIMS, Analytical Chemistry, Drug Product, Manufacturing, Validation Benefits (via System One) Medical, Dental, Vision, 401(k), Life Insurance, and additional voluntary benefits System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#M3- #LI- Ref: #558-Scientific

Apply