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Quality Control Pharmacist Jobs (NOW HIRING)

SRA Trials

Quality Control Specialist

Doral, FL

$25 - $32/hr

QUALITY CONTROL SPECIALIST Clinical Trials Doral, FL • Onsite • Full-Time • Monday to Friday ... We partner with all major pharmaceutical companies and conduct studies across a wide range of ...

Careers at RK Pharma Inc.

QC Chemist

Pearl River, NY · On-site

$55K - $95K/yr

RK Pharma Inc, a vertically integrated pharmaceutical company with our main manufacturing site in Pearl River, NY, is seeking a Quality Control Chemist to work with our growing Quality Teams as we ...

System One

Quality Control Chemist

Boca Raton, FL · On-site

$70K - $90K/yr

Onsite, Monday - Friday Day Overview Developing pharmaceutical CDMO in Boca Raton, FL is seeking an experienced Quality Control Chemist to join their team on a direct hire basis! Responsibilities

Sebela Pharma

QC Chemist

Holbrook, MA · On-site

$55K - $60K/yr

Sebela Pharmaceuticals is a U.S. pharmaceutical company with a market-leading position in ... The QC Chemist is a laboratory bench position that performs routine release testing for raw ...

AMRI

Customer Quality Lead (QC)

Rensselaer, NY

Curia provides global contract research and manufacturing services to the pharmaceutical and ... The customer quality lead for QC will be part of the leadership team and will be accountable to ...

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Quality Control Pharmacist information

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How much do quality control pharmacist jobs pay per hour?

As of Aug 16, 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 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.

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.
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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, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $126,701 per year, or $60.9 per hour.

Quality Control Manager

Granules Pharmaceuticals

Chantilly, VA

$100K - $120K/yr

Full-time

Re-posted 26 days ago

Job description

Description

Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD.  Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US!

With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.

We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.

Job Summary


Supervise the work of laboratory personnel engaged in performing routine finished product testing & stability testing, including planning laboratory work, evaluating work performed and handling procedural and technical laboratory problems. Execute according to high standards of quality at the lab through managing and continuously improving the effectiveness of laboratory quality processes and systems 

Job Duties & Responsibilities


  • Supervise the testing of bulk release, finished product and stability testing 
  • Manage and supervise QC laboratory personnel with varying levels of experience, assigning the work schedule and ensure assigned tasks are performed.
  • Review of test results for accuracy and proper documentation.
  • Review of specifications and STMs for in process and finished products.
  • Write OOS investigations, including finding root cause and corrective/preventive actions.
  • Supervise lab processes, including timely management of investigations, CAPA implementation to ensure sustainable compliance
  • Review of SOPs, lab related investigations, stability failure notifications, COAs, and compilation of stability related data. Responsible for timely release of in-process, finished product release COA's
  • Monitor and report the trends in bulk, finished products, and stability samples to QC/QA Management
  • Review of IQ, OQ, and PQ for new instruments, protocols/reports
  • Responsible for coordinating with other departments like warehouse, QA, Maintenance, purchase department, R&D in day to day activity for better operational requirements and to follow the cGMP requirements.
  • Responsible for the coordination of sample management, not limited to in-process, finished product and stability samples.
  • Monitor Quality Control, Safety and cGMP practices to assure compliance with internal and external regulations.
  • Perform other related duties as assigned to meet departmental and Company objectives.


Management Responsibility 


  • Manage group of scientists.


Reports to

  • Associate Director / Director

Requirements

Knowledge & Skills 


  • Ability to maintain integrity and honesty at all times
  • Ability to communicate and lead with transparency
  • Accountable for performance and results of department
  • Ability to assume additional responsibilities on own initiative.


Experience & Education


  • Requires minimum BA/BS in Biochemistry, Chemistry or related field with 10-15 years' experience in the biotech or pharmaceutical industry. Management experience in Quality Control required MS/MA.


Physical Requirements/Working Environment


  • Regular Laboratory environment with lab coats, safety glasses, 4-6hrs/day of standing while performing chemical test and able to stand for 4-6hrs/day.


Travel 


  • No Travel requirement.


Disclaimer


The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.



We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.

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