ZipRecruiter

Log In

1

Pharma Qc Jobs (NOW HIRING)

Careers at RK Pharma Inc.

QA Associate

Pearl River, NY · On-site

$55K - $95K/yr

... * Familiarity with cleanroom operations and environmental monitoring programs * Experience supporting audits or regulatory inspections How We Work At RK Pharma, quality takes priority over speed.

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

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

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 ...

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 ...

next page

Showing results 1-20

All JobsPharma Qc Jobs

Pharma Qc information

See salary details

$16

$27

$41

How much do pharma qc jobs pay per hour?

As of Jul 31, 2026, the average hourly pay for pharma qc in the United States is $27.92, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $31.01 per hour, depending on experience, location, and employer.

What is the difference between Pharma Qc vs Pharma Quality Assurance (QA)?

AspectPharma QcPharma QA
CertificationsGMP, GMP-related trainingGMP, GMP-related training
Work EnvironmentLaboratory testing, sample analysisProcess audits, documentation review
ResponsibilitiesTesting raw materials, in-process, finished productsDeveloping, implementing quality systems, audits
Industry UsageQuality control testing in manufacturingEnsuring compliance, process quality assurance

Pharma Qc and Pharma QA roles both focus on quality in pharmaceutical manufacturing but differ in scope. Pharma Qc primarily involves laboratory testing and sample analysis to ensure product quality, while Pharma QA emphasizes process oversight, audits, and compliance systems. Both roles require GMP knowledge and are essential for maintaining industry standards.

More about Pharma Qc jobs
What cities are hiring for Pharma Qc jobs? Cities with the most Pharma Qc job openings:
What states have the most Pharma Qc jobs? States with the most job openings for Pharma Qc jobs include:
What job categories do people searching Pharma Qc jobs look for? The top searched job categories for Pharma Qc jobs are:
Pharma Qc jobs near you
Infographic showing various Pharma Qc job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 91% Full Time, 2% Part Time, and 4% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $58,065 per year, or $27.9 per hour.

Quality Control Technician (Wilcrest Pharma)

Wilcrest Pharma

Houston, TX • On-site

$19.75 - $25.50/hr

Full-time

Posted 24 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.

Apply