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Quality Control Pharmacist Jobs (NOW HIRING)

Ardena

Scientist - Quality Control (QC)

Somerset, NJ · On-site

Ardena supports pharmaceutical and biotechnology companies in bringing innovative, complex ... Quality Control Location: Somerset, New Jersey FLSA Status: Exempt Employment Type: Full-Time ...

Glenmark Pharmaceuticals

Quality Control Analyst

Monroe, NC · On-site

$22.25 - $30/hr

Glenmark Pharmaceuticals Inc., USA is a subsidiary of Glenmark Pharmaceuticals Ltd., a leading ... This position is for a highly motivated member of the Quality Control (QC) Lab at the Monroe ...

Stark Pharma Solutions Inc

QC Scientist

Irvine, CA · On-site

... Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We ... Position: QC Scientist Location: California Duration: Long Term Job Overview We are seeking a Mid ...

Sebela Pharma

Director, Quality Control

Holbrook, MA · On-site

$150K - $190K/yr

Sebela Pharmaceuticals is a U.S. pharmaceutical company with a market-leading position in ... Direct all QC laboratory activities, in support of GMP Testing, release, and stability programs ...

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 ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

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 ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

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 ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

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 ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

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Quality Control Pharmacist information

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How much do quality control pharmacist jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for quality control pharmacist in the United States is $60.91, according to ZipRecruiter salary data. Most workers in this role earn between $56.01 and $67.31 per hour, depending on experience, location, and employer.

What is a quality control pharmacist?

Quality Control Pharmacists are professionals responsible for ensuring that pharmaceutical products meet established quality standards before they reach consumers. They conduct a variety of tests and analyses to verify the identity, purity, strength, and composition of medications. Their role is crucial in maintaining compliance with regulatory guidelines and ensuring patient safety. They often work in laboratories within pharmaceutical manufacturing companies, collaborating with production and regulatory teams. Quality Control Pharmacists also document their findings and help implement corrective actions when necessary.

What are the key skills and qualifications needed to thrive as a quality control pharmacist?

To thrive as a Quality Control Pharmacist, you need a strong background in pharmaceutical sciences, analytical chemistry, and regulatory compliance, typically supported by a pharmacy degree and relevant licensure. Familiarity with laboratory equipment, chromatographic techniques (like HPLC or GC), and quality management systems (such as GMP) is essential. Attention to detail, problem-solving abilities, and clear communication are crucial soft skills for ensuring accuracy and effective teamwork. These skills and qualifications are vital to maintain product safety, uphold regulatory standards, and ensure the integrity of pharmaceutical products.

What are some common challenges faced by a quality control pharmacist when working with cross-functional teams?

Quality Control Pharmacists often collaborate closely with production, research and development, and regulatory affairs teams. A common challenge is ensuring clear communication regarding testing protocols and results, especially when timelines are tight and multiple departments are involved. Balancing strict regulatory compliance with practical production needs can also create tension, requiring strong problem-solving and negotiation skills. Building strong working relationships and maintaining thorough documentation help navigate these challenges and ensure product quality and safety.

What is the difference between Quality Control Pharmacist vs Quality Assurance Specialist?

AspectQuality Control PharmacistQuality Assurance Specialist
CredentialsPharmacy license, often with GMP or QA certificationsRelevant certifications like CQE or ISO auditor
Work EnvironmentLaboratories, manufacturing plants, pharmaceutical companiesQuality management departments, regulatory agencies
Industry UsageEnsures product quality through testing and analysisDevelops and maintains quality systems and processes

The main difference is that a Quality Control Pharmacist focuses on testing and verifying pharmaceutical products to meet quality standards, while a Quality Assurance Specialist develops and oversees quality systems to prevent issues. Both roles are essential in pharmaceutical manufacturing but serve different functions within the quality management process.

More about Quality Control Pharmacist jobs

What states have the most Quality Control Pharmacist jobs?

States with the most job openings for Quality Control Pharmacist jobs include:

What job categories do people searching Quality Control Pharmacist jobs look for?

The top searched job categories for Quality Control Pharmacist jobs are:

Quality Control Pharmacist jobs near you
Infographic showing various Quality Control Pharmacist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $126,701 per year, or $60.9 per hour.

Scientist - Quality Control (QC)

Ardena

Somerset, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 10 days ago

Job description

About Ardena
Ardena is a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO) specializing in precision medicine development. Ardena supports pharmaceutical and biotechnology companies in bringing innovative, complex molecules from discovery to market.
The Ardena Group operates from five sites across Europe and the United States, employing more than 750 professionals. Ardena's European sites are located in Oss and Assen (the Netherlands), Ghent (Belgium), and Pamplona (Spain). Ardena's U.S. facility is based in Somerset, New Jersey.
For our Somerset, New Jersey site, we are looking for a Scientist - Quality Control (QC) to join our Quality Assurance Division.
Ardena provides integrated services spanning drug substance development, drug product formulation, GMP manufacturing, bioanalytical services, clinical logistics, fill and finish, and CMC regulatory support.
Job Overview
Position: Scientist - Quality Control (QC)
Division: Quality Assurance
Department: Quality Control
Location: Somerset, New Jersey
FLSA Status: Exempt
Employment Type: Full-Time
Ardena is seeking a Scientist - Quality Control (QC) to join our Quality Control team in Somerset, NJ. This role supports pharmaceutical development and commercial manufacturing by performing analytical testing of raw materials, in-process materials, finished products, and stability samples within a GMP-regulated laboratory environment.
The successful candidate will perform laboratory testing using a variety of analytical techniques while ensuring compliance with cGMP, data integrity, and regulatory requirements. This position offers the opportunity to contribute directly to the quality, safety, and timely release of pharmaceutical products supporting patients worldwide.
Role Description
As a Scientist - Quality Control (QC) at Ardena, you will independently perform analytical testing and support quality control activities for clinical and commercial pharmaceutical products. You will analyze laboratory data, interpret results, investigate deviations, and communicate findings through technical reports and documentation.
Working in a GMP-regulated laboratory, you will collaborate closely with cross-functional teams including Quality Assurance, Manufacturing, Regulatory Affairs, Project Management, and other technical departments to ensure projects are completed on schedule while maintaining the highest standards of quality and compliance.
Key Responsibilities
  • Perform analytical testing of raw materials, in-process materials, finished products, and stability samples to support pharmaceutical development and commercial manufacturing.
  • Independently execute laboratory testing with accuracy while maintaining complete and compliant documentation.
  • Analyze laboratory data, evaluate results for accuracy and integrity, and communicate findings through technical reports and presentations.
  • Perform Quality Control activities required to meet project timelines and customer deliverables.
  • Utilize analytical techniques including, but not limited to:
    • High Performance Liquid Chromatography (HPLC/LC)
    • Gas Chromatography (GC)
    • Dissolution Testing
    • Standard Wet Chemistry
  • Operate laboratory instrumentation and electronic systems including CDMS, LIMS, ELN, and other laboratory software.
  • Review analytical data for completeness, accuracy, and compliance with regulatory and data integrity requirements.
  • Conduct and document laboratory investigations, deviations, and change management activities.
  • Author and review analytical methods, protocols, reports, specifications, and Standard Operating Procedures (SOPs).
  • Collaborate with cross-functional teams to ensure project objectives and customer timelines are achieved.
  • Support Quality Systems and laboratory infrastructure initiatives.
  • Maintain compliance with cGMP, Health, Safety, Environmental, and Data Integrity requirements.
  • Perform additional technical and administrative duties as assigned.
Profile & Qualifications
Required Qualifications
  • Associate's degree in Chemistry or Analytical Chemistry with 5+ years of experience supporting pharmaceutical product development and manufacturing,

OR
  • Bachelor's degree in Chemistry or Analytical Chemistry with 3+ years of experience supporting pharmaceutical product development and manufacturing.
  • Experience working within a GMP-regulated pharmaceutical laboratory.
  • Strong understanding of analytical chemistry principles and pharmaceutical Quality Control practices.
  • Experience performing analytical testing using chromatographic and wet chemistry techniques.
  • Proficiency with analytical instrumentation, including LC (HPLC), GC, and Dissolution systems.
  • Experience using laboratory electronic systems such as CDMS, LIMS, and Electronic Laboratory Notebooks (ELN).
  • Strong organizational, analytical, and problem-solving skills.
  • Excellent verbal and written communication skills.
  • Ability to effectively manage multiple priorities while meeting project deadlines.
  • Fluent in English, both written and spoken
Preferred Qualifications
  • Experience supporting pharmaceutical development and commercial manufacturing environments.
  • Working knowledge of cGMP, FDA regulations, and data integrity requirements.
  • Experience authoring or reviewing SOPs, analytical methods, laboratory investigations, deviations, and technical reports.
  • Proficiency with Microsoft Office applications, including Teams, Word, Excel, and PowerPoint.
  • Experience working collaboratively with cross-functional technical teams.
  • Alignment with Ardena's CARE values:
    • Communicative
    • Accountable
    • Reliable
    • Excellent
Physical Requirements
  • Ability to occasionally lift up to 15 pounds.
  • Ability to work within laboratory, manufacturing, and office environments.
  • Frequent use of computers and laboratory instrumentation.
  • Ability to read and interpret technical documentation.
  • Must be capable of wearing required Personal Protective Equipment (PPE), including safety glasses, respirators (when required), and safety shoes.
  • Must successfully complete required safety and OSHA training, including respirator fit testing.
  • Ability to work in temperature- and humidity-controlled laboratory environments.
What Ardena Offers
Ardena is a science-driven and people-focused employer. Working at Ardena means contributing to pharmaceutical projects that support the availability, safety, and quality of medicines for patients worldwide.
Ardena offers an international working environment where employees are encouraged to develop their expertise, take ownership, and grow their careers across functions and locations.
Benefits and perks at Ardena include:
  • Competitive salary and comprehensive benefits package.
  • Paid time off and company-recognized holidays.
  • Medical, dental, vision, life, and disability insurance.
  • 401(k) retirement savings plan with company match.
  • Professional development and training opportunities.
  • Collaborative international work environment across Europe and the United States.
  • Opportunities to contribute to innovative pharmaceutical development projects that improve patient health.
  • A values-driven culture guided by Ardena's CARE principles: Communicative, Accountable, Reliable, and Excellent.
How to Apply
Ready to advance your career in pharmaceutical Quality Control?
Apply today through the Ardena Careers website at careers.ardena.com and become part of a team dedicated to advancing pharmaceutical innovation and improving patient lives worldwide.
Department Quality Assurance Locations Somerset (New Jersey, US)

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