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Quality Control Analyst Hplc Jobs in Florida (NOW HIRING)

Quality Control Analyst I

Sunrise, FL · On-site

$23 - $30.75/hr

Quality Control Analyst 5 Months (possible extension) Sunrise, FL Shift Scheduled: Monday to Friday ... Solid understanding of the principles of analytical chemistry as it applies to HPLC, GC, FTIR, UV ...

Quality Control Analyst

Miami, FL · On-site

$23 - $30.75/hr

Job purpose The Quality Control Analyst is responsible for performing and managing results of quality control testing for human tissue donors, recovered tissues, and final processed grafts. The QCA ...

Quality Control Analyst

Miami, FL · On-site

$23 - $30.75/hr

Job purpose The Quality Control Analyst is responsible for performing and managing results of quality control testing for human tissue donors, recovered tissues, and final processed grafts. The QCA ...

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Quality Control Analyst Hplc information

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.

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 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 are popular job titles related to Quality Control Analyst Hplc jobs in Florida? For Quality Control Analyst Hplc jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Quality Control Analyst Hplc jobs in Florida look for? The top searched job categories for Quality Control Analyst Hplc jobs in Florida are:
What cities in Florida are hiring for Quality Control Analyst Hplc jobs? Cities in Florida with the most Quality Control Analyst Hplc job openings:
Infographic showing various Quality Control Analyst Hplc job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.

Quality Control Analyst - Chemistry

Strive Pharmacy

Alachua, FL

$65K - $75K/yr

Full-time

Posted 19 days ago


Strive Pharmacy rating

6.8

Company rating: 6.8 out of 10

Based on 16 frontline employees who took The Breakroom Quiz

57th of 112 rated pharmacies


Job description

Position Overview:

The QC Analyst - Chemistry will perform analytical chemistry testing and support Quality operations in a GMP laboratory environment. The ideal candidate will be very detail-oriented, have hands-on experience with analytical instrumentation, strong documentation skills, and the ability to work efficiently and effectively in a fast-paced setting.

Reports to: Director of Quality

Location: Alachua, FL 

Schedule: Monday - Friday, dayshift

Salary Range: $65,000 - $75,000

Key Responsibilities: 

  • QC Analyst - Chemistry activities to include, supporting method selection and development, supporting method transfer, qualification and validation, monitoring routine use, and supporting investigation records.
    • Support method transfer/qualification/validation activities 
    • Assists in developing, troubleshooting, optimizing complex QC procedures according to regulatory requirements.
    • Collaborate with department personnel to ensure analysts are trained on newly transferred/qualified/validated procedures.
    • Analyze, document, and report experimental data in accordance to Strive requirements
    • Collect/evaluate data trends to ensure qualified/validated methods remain in a state of control.
  • Provide support to the Quality Control team as needed.
    • Train analysts on analytical techniques
    • Troubleshoot assay failures
    • May require occasional early morning, late evening, and / or weekend work
  • Perform analytical testing (GC, HPLC, FTIR) on raw materials and finished products.
  • Review, organize and maintain laboratory documentation and records.
  • Ensure compliance with GMP, safety, regulatory and corporate requirements.
  • Conduct Out-of-Specification (OOS) and Out-of-Trend investigations.
  • Work directly with vendors.
  • Other activities as assigned.

Qualifications:

  • BS in a Chemical Science field (Biochemistry, Analytical Chemistry, etc.), or related field and 2+ years of applicable industry experience.
  • Experience with cGMPs applicable to the pharmaceutical industry.
  • Strong verbal / written and interpersonal communication skills as a team player and willing to work in an environment where individual initiative, collaboration and accountability are valued.
  • Analytical problem-solving and troubleshooting skills.
  • Adaptable and flexible in response to a dynamic operating environment.
  • Solid understanding of laboratory practices and analytical activities.
  • Ability to prioritize and balance multiple tasks.
  • Proficiency with database applications.
  • Ability to work efficiently in a team environment.
  • Ability to interpret technical information, strong problem-solving skills.

Preferred Qualifications: 

  • Experience with HPLC/UPLC assay and ID testing.
  • Experience in a compounding pharmacy or outsourced testing facility.

Position and compensation levels are commensurate with level of education and experience.

Role/Site Specific Requirements:

This position may also include the following:

  • This role is primarily a Sedentary role. This can include exerting up to 30 pounds of force to move objects.
  • Visual acuity such as: working with data & figures, viewing computer terminal, extensive reading, operating machinery, general observations of facilities, etc.
  • Participation in an occupational health program which can include; medical assessment, surveillance, vaccination, and testing
  • Use of personal protective equipment which can include respirators, Personal Air Purifying Respirators [PAPR], gowns, gloves, face protection, other barrier equipment, etc.

Exposure to the following:

  • Use of personal protective equipment (which can include respirators, Personal Air Purifying Respirators (PAPR), gowns, gloves, face protection, other barrier equipment, etc.
  • Handling, managing, disposing hazardous and non-hazardous waste (which can include: chemicals, universal and e-wastes, oil, aqueous wastewater, etc.).
  • Working in laboratories & production rooms, waste holding areas, or other facilities where hazardous chemicals may be stored or handled.

The items described here are representative of those that must be met to successfully perform the essential functions of this job.


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