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Pharmaceutical Quality Control Jobs (NOW HIRING)

Garonit Pharmaceutical

QC Supervisor

Fairfield, NJ · On-site

Bachelor's degree in Chemistry or a related scientific field. * 2+ years in a supervisory or management role in a pharmaceutical QC lab. * Strong experience with Empower 3, HPLC, GC, and wet ...

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 ...

Cipla

Quality Control (QC) Chemist

Fall River, MA

$65K - $105K/yr

Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) * Evaluate critical quality attributes (CQA) such as particle ...

Cipla

Quality Control (QC) Chemist

Fall River, MA · On-site

$65K - $105K/yr

Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) * Evaluate critical quality attributes (CQA) such as particle ...

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 ...

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 Holdings, LLC

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 ...

Cipla

$65K - $105K/yr

What You'll Do Analytical Testing & Expertise Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) Evaluate critical ...

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Pharmaceutical Quality Control information

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$10

$27

$50

How much do pharmaceutical quality control jobs pay per hour?

As of Jul 21, 2026, the average hourly pay for pharmaceutical quality control in the United States is $27.14, according to ZipRecruiter salary data. Most workers in this role earn between $18.99 and $33.65 per hour, depending on experience, location, and employer.

What are some typical daily tasks for someone working in Pharmaceutical Quality Control?

A typical day in Pharmaceutical Quality Control involves performing laboratory tests and analyses on raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with safety and regulatory standards. You may prepare and calibrate lab equipment, document test results, review batch records, and assist in investigations of deviations or out-of-specification findings. Additionally, collaboration with production, research, and quality assurance teams is common to maintain continuous improvement and address any quality issues quickly. This role is detail-oriented and often includes both routine testing and problem-solving activities, making each day varied and impactful.

What is the role of quality control in pharmaceuticals?

In pharmaceutical quality control, professionals are responsible for testing raw materials, in-process samples, and finished products to ensure they meet safety, efficacy, and quality standards. They use analytical techniques and adhere to Good Manufacturing Practices (GMP) to detect and prevent contamination, defects, or deviations, ensuring consistent product quality and regulatory compliance.

What are the key skills and qualifications needed to thrive in the Pharmaceutical Quality Control position, and why are they important?

Pharmaceutical Quality Control professionals need a solid background in chemistry, biology, or pharmacy, often supported by a relevant degree and industry knowledge. Familiarity with laboratory instrumentation, Good Manufacturing Practices (GMP), and quality management systems, along with certifications like ASQ or GxP training, is highly beneficial. Attention to detail, strong analytical thinking, and clear communication are key soft skills that drive accuracy and collaboration. These competencies are crucial for ensuring that pharmaceutical products meet strict safety, efficacy, and regulatory standards.

Does QA or QC pay more?

In pharmaceutical quality control, Quality Assurance (QA) roles typically offer higher salaries than Quality Control (QC) positions due to their broader responsibilities in process oversight and compliance. However, pay can vary based on experience, certifications, and location, with QA often requiring more managerial or analytical skills. Both roles are essential for ensuring product quality and safety in the industry.

What is a Pharmaceutical Quality Control job?

A Pharmaceutical Quality Control (QC) job involves ensuring that medications meet required safety, efficacy, and quality standards before distribution. Professionals in this field conduct tests, analyze raw materials and finished products, and ensure compliance with regulatory guidelines like Good Manufacturing Practices (GMP). They use analytical techniques such as HPLC, spectroscopy, and microbiological testing. QC specialists also document findings, investigate deviations, and collaborate with other departments to resolve quality issues. Their work helps maintain product integrity and patient safety.

Is QC a high paying job?

Quality Control (QC) roles in the pharmaceutical industry can offer competitive salaries, especially with experience, certifications, and specialized skills such as analytical testing or regulatory knowledge. Salaries vary by location, company, and level of responsibility, but QC positions are generally considered to be well-paying within the industry.

What is the highest salary in QA Pharma?

The highest salaries for Pharmaceutical Quality Control professionals can reach over $100,000 annually, especially for senior roles with extensive experience, advanced certifications, or managerial responsibilities. Salaries vary based on location, company size, and individual expertise, with top earners often working in large pharmaceutical companies or specialized environments.
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Pharmaceutical Quality Control jobs near you
QC Supervisor

QC Supervisor

Garonit Pharmaceutical

Fairfield, NJ • On-site

Other

This job post has expired today. Applications are no longer accepted.

Job description

QC Supervisor

Onsite in Fairfield, NJ

We're looking for a QC Supervisor who's both a hands-on technical expert and a strong leader. This role manages the daily operations of our QC Laboratory - leading testing, method development, and data review while ensuring full cGMP compliance.

 What You'll Do

  • Supervise and lead a team of QC chemists and analysts.
  • Oversee all analytical testing for manufacturing, release, and stability.
  • Review and interpret HPLC, GC, and wet chemistry data in compliance with cGMP.
  • Author and review SOPs, analytical methods, and validation protocols.
  • Conduct and support laboratory investigations, CAPA, and change controls.
  • Manage and schedule lab workloads to meet production timelines.
  • Ensure lab safety, data integrity, and adherence to FDA and ICH guidelines.
  • Collaborate cross-functionally to resolve quality-related issues quickly.
  • Develop and mentor QC staff through training and performance development.
  • Support continuous improvement initiatives to enhance compliance and efficiency.

 What You'll Bring

  • Bachelor's degree in Chemistry or a related scientific field.
  • 2+ years in a supervisory or management role in a pharmaceutical QC lab.
  • Strong experience with Empower 3, HPLC, GC, and wet chemistry.
  • Deep understanding of cGMP, ICH, CFR, and USP testing requirements.
  • Experience in method development, validation, and stability testing.
  • Proven leadership, training, and coaching skills.
  • Excellent problem-solving, documentation, and communication abilities.
  • High attention to detail, strong work ethic, and commitment to quality.

 Why Garonit Pharma

  • Work with cutting-edge equipment in a collaborative, growth-oriented environment.
  • Play a key role in ensuring product quality and regulatory success.
  • Competitive compensation and career growth opportunities.

Apply