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Quality Control Analyst Pharmaceutical Jobs (NOW HIRING)

Astrix Inc

Quality Control Analyst III

Rensselaer, NY · On-site

$23.75 - $32/hr

This role is ideal for an analytical scientist with pharmaceutical laboratory experience who enjoys ... Provide backup support for QC analytical instrument maintenance and calibration. * Maintain general ...

Curia, Inc.

Quality Control Analyst II

Rensselaer, NY · On-site

$23.75 - $32/hr

Quality Control Analyst II in Rensselaer, NY - Nights Build your future at Curia, where our work ... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ...

AMRI

Quality Control Analyst II

Rensselaer, NY

$23.75 - $32/hr

Quality Control Analyst II in Rensselaer, NY - Nights Build your future at Curia, where our work ... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ...

Astrix Inc

QC Analyst II (Chemistry)

Rensselaer, NY · On-site

$30 - $47/hr

Candidates with strong analytical chemistry, chromatography, and pharmaceutical QC laboratory experience are highly encouraged to apply. Key Responsibilities * Perform analytical testing for incoming ...

Laboratoire Guerbet

QC Analyst

Raleigh, IL · On-site

$22.75 - $30.75/hr

QC Analyst At Guerbet, we build lasting relationships so that to enable people to live better ... We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals ...

TekWissen LLC

Quality Control Analyst

Vacaville, CA · On-site

$20 - $25/hr

Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom ... Job Title: QC Associate / Quality Control Analyst I Location: Vacaville, CA - 95688 Duration: 6 ...

Guerbet

QC Analyst

Raleigh, IL · On-site

$22.75 - $30.75/hr

QC Analyst At Guerbet, we build lasting relationships so that to enable people to live better ... We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals ...

Manpower

Quality Control Analyst - Chemistry

Myerstown, PA

$23 - $31/hr

Our client, a leading organization in pharmaceutical manufacturing, is seeking a dedicated and detail-oriented Quality Control Analyst - Chemistry to join their team. As a Quality Control Analyst ...

New

ARUP

Quality Control Analyst

South Jordan, UT · On-site

$22.75 - $30.50/hr

The Quality Control Analyst provides analytical expertise to the laboratories regarding the department Quality Control program. Evaluates and implements protocols and methods of quality control to ...

ARUP

Quality Control Analyst

Salt Lake City, UT

$23.25 - $31.25/hr

The Quality Control Analyst provides analytical expertise to the laboratories regarding the department Quality Control program. Evaluates and implements protocols and methods of quality control to ...

ARUP Laboratories

Quality Control Analyst

South Jordan, UT

$22.75 - $30.50/hr

The Quality Control Analyst provides analytical expertise to the laboratories regarding the department Quality Control program. Evaluates and implements protocols and methods of quality control to ...

Kellton Tech

QC Analyst II

Vacaville, CA · On-site

$28/hr

Position: QC Analyst II Location: Vacaville, CA (Onsite) Pay Rate : $28/hr. on W2 Summary Under ... Preferred disciplines: scientific fields within pharmaceutical or biopharmaceutical industry.

Colorcon

QC Analyst I

Chalfont, PA · On-site

$23.25 - $31.25/hr

QC Analyst I Colorcon ® is a world leader in the development, supply and technical support of ... pharmaceutical, nutritional, and animal health industries. Our best-in-class products and ...

DISCGENICS INC

Quality Control Analyst

Salt Lake City, UT · On-site

$23 - $31/hr

The QC Analyst performs quality control analysis of raw material, and finished product using USP ... Experience in Pharmaceutical, Biologics, Medical Device or Cell/Gene Therapy industry. * Preferred:

Cellares

Quality Control Analyst

Bridgewater, NJ · On-site

$24.50 - $33/hr

We are seeking an innovative, creative, and detail-oriented Quality Control Analyst to join our ... Knowledge of pharmaceutical cGMP (US and EU) is preferred * Must have excellent verbal, written ...

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

As of Jun 10, 2026, the average hourly pay for quality control analyst pharmaceutical 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 the key skills and qualifications needed to thrive in the Quality Control Analyst Pharmaceutical position, and why are they important?

To thrive as a Quality Control Analyst Pharmaceutical, you need a solid background in chemistry or biology, familiarity with laboratory testing procedures, and a relevant bachelor's degree. Hands-on experience using laboratory instruments like HPLC, GC, and LIMS, along with knowledge of GMP and regulatory guidelines, is highly valued. Strong attention to detail, problem-solving skills, and effective communication are key soft skills for this position. These abilities ensure accurate testing, regulatory compliance, and the consistent delivery of safe, high-quality pharmaceutical products.

What is a Quality Control Analyst Pharmaceutical job?

A Quality Control Analyst in the pharmaceutical industry is responsible for testing and analyzing drugs and raw materials to ensure they meet regulatory standards and company specifications. They conduct laboratory tests, document findings, and identify any deviations from quality standards. Their role is critical in maintaining product safety, efficacy, and compliance with guidelines set by regulatory agencies such as the FDA or EMA. They often work with techniques like HPLC, GC, and spectroscopy to assess product quality.

What are some typical daily responsibilities for a Quality Control Analyst in the pharmaceutical industry?

A Quality Control Analyst in the pharmaceutical industry is responsible for conducting a variety of laboratory tests on raw materials, in-process samples, and finished products to ensure they meet strict quality standards. Day-to-day tasks often include preparing and analyzing samples, documenting test results, troubleshooting equipment, and collaborating with other departments such as production and quality assurance. You may also be involved in investigating out-of-specification results, maintaining laboratory records, and participating in internal audits. This role is integral to maintaining compliance with regulatory requirements and ensuring patient safety, making accuracy and attention to detail essential.

What is the role of a QC analyst in pharma?

A Quality Control (QC) analyst in the pharmaceutical industry is responsible for testing raw materials, in-process samples, and finished products to ensure they meet quality standards and regulatory requirements. They use laboratory techniques, such as chromatography and spectrometry, and maintain detailed documentation to support product safety and efficacy. QC analysts often work in controlled environments and may require certifications like GMP training.
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Quality Control Analyst Pharmaceutical jobs near you
Infographic showing various Quality Control Analyst Pharmaceutical job openings in the United States as of June 2026, with employment types broken down into 67% Full Time, 14% Part Time, 14% Temporary, and 5% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% 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

Astrix Inc

Rensselaer, NY • On-site

$23.75 - $32/hr

Contractor

Posted 11 days ago

Job description

Pay Rate Low: 30.63 | Pay Rate High: 45.95
Astrix is proud to partner with our client- a leading force in contract research, development, and manufacturing within the pharmaceutical and biotech space- to find top-tier talent.
We are currently seeking a Quality Control Analyst II to join a growing QC team in Rensselaer, NY for a 6 month contract agreement with the possibility of extension. This role is ideal for an analytical scientist with pharmaceutical laboratory experience who enjoys hands-on testing, problem solving, and working in a regulated environment supporting drug product quality.
If you are passionate about science and want to contribute to the development and manufacturing of life-saving therapies, this is an exciting opportunity to make a meaningful impact.
Schedule: 6:00 PM - 6:00 AM
Responsibilities
  • Perform analytical testing of incoming raw materials, in-process samples, finished products, and stability samples using laboratory equipment such as balances, pipettes, pH meters, UV/Visible spectrophotometers, and Total Organic Carbon analyzers.
  • Conduct chromatographic analysis including HPLC, GC, and UPLC with minimal supervision following established methods and procedures.
  • Perform wet chemistry and analytical assays, including testing by HPLC, GC, IR, UV, and other analytical techniques.
  • Support raw material testing and sampling in accordance with established quality procedures.
  • Provide backup support for QC analytical instrument maintenance and calibration.
  • Maintain general laboratory equipment, ensure proper laboratory housekeeping, and support preparation activities for internal and external audits.
  • Perform or assist with method qualifications, method transfers, and validation activities within the QC laboratory.
  • Assist with analytical method development initiatives.
  • Support cleaning validation studies and related testing activities.
  • Assist in the evaluation and implementation of new laboratory equipment and processes.
  • Review QC data and provide summaries and reports to management as needed.
  • Assist QC management with investigations related to OOS results, deviations, and CAPAs.
  • Provide backup support for analytical sample receipt and logistics, including sample login, shipment to external labs, tracking, distribution of test results, and documentation closure.

Qualifications
  • Bachelor's degree in Chemistry or a related scientific discipline
  • 3-5 years of experience in a pharmaceutical or regulated laboratory environment, or an equivalent combination of education and experience

Preferred Qualifications
  • Experience working in a cGMP or GLP pharmaceutical environment
  • Hands-on experience with chromatographic techniques (HPLC, GC, UPLC) and analytical instrumentation
  • Experience supporting method validation, method transfer, or quality investigations
** This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you**
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