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Quality Control Analyst Pharmaceutical Jobs (NOW HIRING)

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

Quality Control Analyst

Smithfield, PA · On-site

$24.50 - $32.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Control Analyst Job title: Quality Control Analyst Location: Smithfield, PA At Johnson Matthey, your work will matter. As a Quality Control Analyst, you'll join a world leader in platinum ...

Quality Control Analyst

Smithfield, PA

$24.50 - $32.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Control Analyst Location: Smithfield, PA At Johnson Matthey, your work will matter. As a Quality Control Analyst,you'lljoin a world leader in platinum group metals with over 200 years of ...

QC Analyst

Los Angeles, CA · On-site

$25.75 - $34.75/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Position Overview The QC Analyst is an analytical, process driven, and detail-oriented professional responsible for supporting Arixa Capital's data quality across the loan lifecycle. This role ...

Quality Control Analyst

Saint Louis, MO · On-site

$24/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience in a quality control, manufacturing, pharmaceutical, consumer products, personal care ... Analytical Testing * Data Collection & Analysis * Quality Control * Attention to Detail

New

QC Analyst

Los Angeles, CA · Hybrid

$25.75 - $34.75/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Position Overview The QC Analyst is an analytical, process driven, and detail-oriented professional responsible for supporting Arixa Capital's data quality across the loan lifecycle. This role ...

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.

QC Analyst

Los Angeles, CA · Hybrid

$25.75 - $34.75/hr

The QC Analyst will analyze data for consistency, identify discrepancies, correct mistakes, and provide feedback and training to the operational teams to avoid future inconsistencies. This position ...

QC Analyst

Phoenix, AZ · Hybrid

$23.75 - $32/hr

The QC Analyst will analyze data for consistency, identify discrepancies, correct mistakes, and provide feedback and training to the operational teams to avoid future inconsistencies. This position ...

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 ...

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

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 ...

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

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 ...

QC Analyst

Carlsbad, NM

$70K - $130K/yr

  • Medical

  • Life

  • Retirement

  • PTO

As a QC Analyst, you will play a critical role in generating reliable analytical data that supports ... Administration regulated pharmaceutical manufacturing environment. * Knowledge of Good ...

Quality Control Analyst

Ridgefield, NJ · On-site

$23.95/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Adecco is currently assisting a local Customer in their search for Quality Control Analyst positions in Ridgefield, NJ. This is a great opportunity to further your existing skills as a Quality ...

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 ... Pharmaceutical, etc.) will be considered. Laboratory Skills: Aseptic techniques, bioburden ...

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 ... Pharmaceutical, etc.) will be considered. Laboratory Skills: Aseptic techniques, bioburden ...

QC Analyst (Pharma)

Ventura, CA · On-site

$39 - $41/hr

Perform routine QC laboratory testing using analytical techniques including pH, Osmolality, and FT ... Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or a related ...

Showing results 21-40

Quality Control Analyst Pharmaceutical information

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

As of Aug 14, 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 skills and qualifications are needed to be a quality control analyst pharmaceutical?

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.

Is a quality control analyst pharmaceutical a stressful job?

A quality control analyst in pharmaceuticals can experience stress due to strict regulatory standards, tight deadlines, and the need for precise testing and documentation. However, the job often involves routine procedures, controlled environments, and the use of analytical tools, which can help manage workload and reduce stress levels.

What is a quality control analyst pharmaceutical?

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 does a quality control analyst pharmaceutical do?

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.

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Infographic showing various Quality Control Analyst Pharmaceutical job openings in the United States as of August 2026, with employment types broken down into 79% Full Time, 14% Contract, and 7% Nights. Highlights an 100% In-person job distribution, with an average salary of $58,065 per year, or $27.9 per hour.

Quality Control Analyst

TekWissen LLC

Vacaville, CA • On-site

$20 - $25/hr

Contractor

Re-posted 27 days ago


Job description

Overview:  

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.   Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.  

Job Title:       QC Associate / Quality Control Analyst I
Location:       Vacaville, CA - 95688
Duration:       6 Months
Job Type:       Temporary Assignment     
Work Type:   Onsite

Summary
 
With limited supervision, the QC Associate I is responsible for performing direct materials testing in compliance with cGMP regulations. The role involves executing laboratory testing, reviewing and trending data, supporting investigations (OOS, OOT, OOE), and contributing to laboratory operations and quality objectives. The position works closely with Quality Control leadership to meet departmental and organizational goals.

Responsibilities

  • Perform basic to moderately complex laboratory testing in compliance with GMP requirements
  • Review, analyze, and assess test data against established acceptance criteria
  • Conduct technical review of peer-generated data
  • Perform trend analysis and assist in establishing limits
  • Identify discrepancies and support quality investigations and CAPA initiatives
  • Troubleshoot technical and testing-related issues
  • Identify gaps in systems, procedures, and laboratory practices
  • Participate in assay transfer, assay validation, and method-related activities
  • Perform equipment qualification, calibration, and routine maintenance
  • Prepare and maintain standards, controls, stocks, cultures, and reagents per procedures
  • Ensure GMP compliance across laboratory operations
  • Support internal and external audits and regulatory inspections
  • Coordinate with internal customers to support multi-site operations
  • Meet assigned schedules, timelines, and deadlines (95% on-time performance expectation)
  • Participate in or lead team projects, process improvements, and continuous improvement initiatives
  • Write protocols, reports, and technical documentation under limited supervision
  • Provide and receive training as required
  • Perform additional duties as assigned to support Quality activities
Required Skills
  • Bachelor’s degree (B.S./B.A.) in a relevant scientific discipline with 1–3 years of industry experience OR
  • Master’s degree with at least 1 year of relevant experience
  • Experience in the pharmaceutical or biopharmaceutical industry
  • Hands-on experience with analytical and/or biological testing procedures
  • Strong understanding of cGMP regulations and quality systems
  • Experience with OOS, OOT, and OOE investigations
  • Exposure to assay transfer, assay validation, and method lifecycle activities
  • Experience supporting regulatory inspections (FDA, EMA, etc.)
  • Familiarity with trend analysis and data integrity practices
  • Prior involvement in process improvement or cross-functional projects
  • Experience working in multi-site or global operational environments
  • Ability to apply scientific principles, theories, and techniques in a QC environment
  • Strong verbal and written communication skills
  • Sound judgment, analytical thinking, and problem-solving abilities
  • Ability to work independently with limited supervision and manage short-term priorities
TekWissen® Group is an equal opportunity employer supporting workforce diversity.

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 


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About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

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