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Quality Control Pharma Jobs (NOW HIRING)

Tris Pharma

QC Analytical Chemist

Monmouth Junction, NJ · On-site

$90K/yr

Tris Pharma, Inc. (www.trispharma.com) is a leading privately-owned U.S. biopharmaceutical company ... Our Quality Control Department is growing and we have openings for QC Analytical Chemists at ...

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 ...

PCI Pharma Services

Director, QC

San Diego, CA · On-site

The role oversees QC Chemistry, Method Transfers, Stability, Raw Materials, and Logistics ... Embody PCI Pharma Services' cultural values through daily leadership behaviors, professionalism ...

PCI Pharma Services

Director, QC

San Diego, CA

The role oversees QC Chemistry, Method Transfers,Stability, Raw Materials, and Logistics operations ... Embody PCI Pharma Services' cultural values through daily leadership behaviors, professionalism ...

Randstad

Pharma Lab Quality Control Technician

Norwood, MA · On-site

$30 - $33/hr

Quality Control (QC) Technician Location: On-site (Full-Time Hours) Job Type: Pharma Laboratory Support Environment: GMP QC Bioassay Labs About the Role We are seeking a detail-oriented and reliable ...

Intellectt INC

QA / QC Inspector

Milpitas, CA · On-site

Role: QC Inspector Location: Milpitas, CA - 950335 Duration: 03 Months Schedule: 8:30 AM - 5:30 PM ... Experience in medical device, diagnostic, or pharma-regulated industries. Good Manufacturing ...

Astrix Inc

QC Analyst (Pharma)

Ventura, CA · On-site

$39 - $41/hr

Perform routine QC laboratory testing using analytical techniques including pH, Osmolality, and FT-IR for in-process, finished product, and stability samples. * Support sample management activities ...

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Quality Control Pharma information

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How much do quality control pharma jobs pay per hour?

As of Jul 19, 2026, the average hourly pay for quality control pharma in the United States is $20.97, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $23.08 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Quality Control professional in the pharmaceutical industry, and why are they important?

To thrive as a Quality Control professional in pharma, you need a strong background in chemistry, biology, or a related science, along with knowledge of Good Manufacturing Practices (GMP) and relevant regulations. Familiarity with laboratory instruments (e.g., HPLC, GC), LIMS software, and quality assurance certifications such as ASQ or ISO standards is typically required. Attention to detail, analytical thinking, and effective communication help professionals excel in ensuring product quality and regulatory compliance. These skills ensure that pharmaceutical products are consistently safe, effective, and compliant with industry standards.

What is Quality Control in the pharmaceutical industry?

Quality Control (QC) in the pharmaceutical industry refers to the processes and procedures used to ensure that pharmaceutical products meet required standards of quality, safety, and efficacy. QC professionals test raw materials, in-process samples, and finished products using various analytical techniques to verify that they comply with regulatory specifications. The goal is to detect and prevent defects, ensuring that only products that pass rigorous standards are released to the market. QC is essential for maintaining public health and regulatory compliance in the pharmaceutical sector.

What is the difference between Quality Control Pharma vs Quality Assurance Pharma?

AspectQuality Control PharmaQuality Assurance Pharma
Primary FocusTesting and inspecting raw materials, in-process, and finished products for complianceDeveloping and maintaining quality systems and processes to prevent defects
CertificationsGMP, GLP, relevant laboratory certificationsGMP, ISO 9001, quality management system certifications
Work EnvironmentLaboratories, testing facilitiesQuality departments, documentation, audits
Common Employer RolesPharmaceutical companies, contract labsPharmaceutical companies, regulatory agencies

While both roles aim to ensure product quality, Quality Control Pharma focuses on testing and inspection, whereas Quality Assurance Pharma emphasizes establishing systems and processes to prevent issues. Understanding these differences helps in choosing the right career path or job focus within the pharmaceutical industry.

What are some of the common challenges faced by Quality Control professionals in the pharmaceutical industry?

Quality Control professionals in pharma often face challenges such as staying updated with evolving regulatory standards, managing tight timelines for product release, and ensuring accuracy in complex analytical testing. They must also coordinate closely with production and R&D teams to address any discrepancies or deviations quickly. Maintaining meticulous documentation and effectively handling audits are essential parts of the role, making attention to detail and strong communication skills particularly important.
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Quality Control Pharma jobs near you
Infographic showing various Quality Control Pharma job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.

Quality Control Technician (Wilcrest Pharma)

Wilcrest Pharma

Houston, TX • On-site

$19.75 - $25.50/hr

Full-time

Posted 12 days ago

Job description

What We Are Looking For
As a Quality Control Technician, you will play an important role in helping Wilcrest Pharma deliver safe, high-quality sterile and non-sterile medications. In this role, you will support QC testing activities, sample management, environmental monitoring, finished product inspection, labeling, and packaging support.
What You Will Do
• Collect, prepare, and coordinate samples for third-party testing, ensuring proper chain of custody documentation, storage and timely submission.
• Conduct environmental monitoring (EM) activities including viable air, surface, and personnel monitoring within manufacturing areas.
• Execute assigned qualification and validation activities, including environmental monitoring studies, equipment qualification activities, and sample collection.
• Maintain QC sample inventory, including retention samples, stability samples, and in-process controls, ensuring proper storage and documentation.
• Perform assigned finished product inspection and packaging support activities, including visual inspection, product labeling, label verification/reconciliation, heat sealing, and completion of required documentation.
• Review laboratory and third-party testing data for accuracy, completeness, and compliance with approved specifications.
• Support quality investigations related to out-of-specification (OOS) results, environmental monitoring excursions, inspection discrepancies, labeling issues, and packaging concerns.
• Coordinate with third-party laboratories to schedule routine, release, and stability testing and support timely reporting and documentation of results.
• Support preparation for regulatory inspections, customer audits, and internal audits by helping maintain accurate, complete, and inspection-ready QC documentation.
• Maintain and upload QC records into the electronic documentation management system to support traceability and CGMP compliance.
• Collaborate with Production and other cross-functional teams as needed, and perform additional duties as assigned by the Director of Quality.
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.

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