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Pharmaceutical Quality Control Jobs (NOW HIRING)

QC Analyst II

Fremont, CA ยท On-site

$41/hr

Bachelor's Degree in science or related field * 2-5 years relevant experience in a cGMP pharmaceutical QC environment, or at least 1 year with a Master's degree Physical Requirements * Prolonged ...

Bachelor's degree with 10 years of pharmaceutical Quality experience (preferably in QC) or an equivalent combination of education and experience Additional Information Applicable only to applicants ...

Bachelor's degree with 10 years of pharmaceutical Quality experience (preferably in QC) or an equivalent combination of education and experience Additional Information Applicable only to applicants ...

Bachelor's degree with 10 years of pharmaceutical Quality experience (preferably in QC) or an equivalent combination of education and experience Additional Information Applicable only to applicants ...

Quality Control Analyst

Monroe, NC ยท 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 ...

... pharmaceutical, food, environmental, and clinical industries. Our work helps ensure the safety ... QC Chemist (Raw Materials) to support the launch and operation of a new raw materials testing ...

Director, Quality Control

Holbrook, MA ยท 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 ...

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Pharmaceutical Quality Control information

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How much do pharmaceutical quality control jobs pay per hour?

As of Jul 5, 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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QC Analyst II

Alexza

Fremont, CA โ€ข On-site

$41/hr

Full-time

Posted 6 days ago


Job description

Job Summary
Developing professional expertise, applies company policies and procedures to resolve a variety of issues. Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors. Exercises judgment within defined procedures and practices to determine appropriate action. Builds productive internal/external working relationships.
Responsibilities
  • Provide timely analyses to support manufacturing and stability. This includes routine analyses of raw materials, in process and release of commercial product or clinical supplies
  • Independently perform assays under GMP, maintaining data integrity and ensuring compliance with company SOPs and specifications
  • Provide accurate, written documentation of all work, including detailed observations and conclusions.
  • Under general guidance, participate in laboratory investigations
  • Independently operate, maintain and troubleshoot laboratory instrumentation and equipment in a safe working environment

Skills required
  • Well-organized, capable of multi-tasking, and able to collaborate with individuals in a matrix environment
  • Extensive hands-on experience performing relevant analytical techniques (HPLC, GC, FTIR). Experience with EMPOWER a plus
  • Must have excellent data analysis skills with attention to detail and interpretation of results with a focus on problem solving
  • Excellent written, oral communication skills, and experience with computer software such as WORD, EXCEL, etc.
  • Knowledge of validation requirements for QC methods and regulatory guidelines

Education and Experience Minimum Requirements
  • Bachelor's Degree in science or related field
  • 2-5 years relevant experience in a cGMP pharmaceutical QC environment, or at least 1 year with a Master's degree

Physical Requirements
  • Prolonged periods of sitting at a desk and working on a computer
  • Potentially prolonged periods standing
  • Must be able to lift up to 15 pounds at times
  • Must be willing to travel

Compensation
The base salary for this role starts at $41/hour. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, and relevant education or training. Our compensation package also includes diverse health and other benefits and an annual target bonus for full-time positions.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.