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Pharma Qc Jobs (NOW HIRING)

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 ...

Knowledge of quality control processes in a packaging or manufacturing environment * Familiarity with regulatory compliance requirements * Strong attention to detail and ability to perform meticulous ...

Quality Control

Mebane, NC · On-site

$16.25 - $20.75/hr

... including Pharma, Medical Devices, Aeronautical, Supply Chain, Heavy/Light Industrial, Food ... Title - Measurement Specialist (Quality Control) Location: Mebane, North Carolina, United States ...

Quality Control

Mebane, NC

$16.25 - $20.75/hr

... including Pharma, Medical Devices, Aeronautical, Supply Chain, Heavy/Light Industrial, Food ... Title - Measurement Specialist (Quality Control) Location: Mebane, North Carolina, United States ...

Quality Control

Mebane, NC

$16.25 - $20.75/hr

... including Pharma, Medical Devices, Aeronautical, Supply Chain, Heavy/Light Industrial, Food ... Title - Measurement Specialist (Quality Control) Location: Mebane, North Carolina, United States ...

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QC Technician (2nd Shift)

Apex, NC · On-site

$17 - $20/hr

Körber Pharma Packaging Materials (Formerly Rondo-Pak LLC) Position Description: Quality Control Technician for quality-minded individual with a growing, high-end GMP printing and packaging company ...

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Liquid Industrial Coatings QC Technician Full Time (Elgin, IL- First shift) Our client, a ... Pharma, Food, Energy, Power, Oil & Gas, Chemical, Paints and Petroleum. As market specialists in ...

Quality Control Analyst

Winchester, KY · On-site

$20.75 - $27.75/hr

Quality Control Analyst Position Summary * Typical working hours are on E shift (6 AM- 6 PM ... Other duties as required in support of Catalent Pharma Solutions high performance The Candidate

Quality Control Analyst

Winchester, KY · On-site

$20.75 - $27.75/hr

Quality Control Analyst Position Summary * Typical working hours are Monday-Friday 3 PM - 11:30 PM ... Other duties as required in support of Catalent Pharma Solutions high performance The Candidate

Quality Control Analyst

Winchester, KY · On-site

$20.75 - $27.75/hr

Quality Control Analyst Position Summary * Typical working hours are Monday-Friday 11 PM - 7:30 AM ... Other duties as required in support of Catalent Pharma Solutions high performance The Candidate

Quality Control Technician

Easton, MD

$19 - $24.25/hr

Previous quality control or inspection experience in manufacturing (pharma, food, or regulated industry preferred) * Familiarity with GMP, FDA, or ISO standards is a plus * Strong attention to detail ...

Scientist III, QC

Spokane, WA · On-site

$82 - $131/hr

Jubilant HollisterStier is proudly part of the global, Jubilant Pharma family. established force in ... The QC Scientist III performs the analysis on allergenic and client components, raw materials ...

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Showing results 21-40

Pharma Qc information

See salary details

$16

$27

$41

How much do pharma qc jobs pay per hour?

As of Aug 20, 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:

Infographic showing various Pharma Qc job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 88% Full Time, 6% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 4% Hybrid, and 4% Remote job distribution, with an average salary of $58,065 per year, or $27.9 per hour.

QC Analyst (Pharma)

Astrix Inc

Ventura, CA • On-site

$39 - $41/hr

Full-time, Contractor

Re-posted 3 days ago


Job description

Pay Rate Low: 39 | Pay Rate High: 41
Our client, a global CDMO, offering products and services across the drug development spectrum is looking for a skilled QC Analyst to join their team in Camarillo, CA!
Location: Ventura County, CA
Pay rate: $39- $41/hr.
Job type: 6-month contract (possibility of extension or conversion)
Position Summary
The QC Analyst is responsible for supporting routine laboratory testing, sample management, stability program activities, and quality system requirements within a cGMP-regulated environment. This role ensures accurate testing, documentation, and data integrity while collaborating cross-functionally to support product quality and operational timelines.
Key Responsibilities
  • 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 including sample receipt, login, labeling, tracking, storage, inventory control, and shipment coordination.
  • Assist with execution of the stability program, including sample pulls, submissions, inventory management, tracking, and documentation activities.
  • Maintain accurate and complete documentation in compliance with cGMP, ALCOA+, data integrity requirements, and company procedures.
  • Record and review laboratory data in notebooks, worksheets, logbooks, and electronic systems, ensuring records remain audit-ready at all times.
  • Participate in laboratory investigations related to out-of-specification (OOS) results, deviations, invalid assays, and other quality events.
  • Support laboratory maintenance activities including equipment calibration, routine housekeeping, inventory management, and inspection readiness.
  • Collaborate with Quality Assurance (QA), Manufacturing, Stability, Microbiology, and external testing laboratories to ensure timely completion of testing and operational objectives.
  • Follow approved Standard Operating Procedures (SOPs), test methods, and GMP laboratory procedures with minimal supervision.

Qualifications
  • Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline preferred.
  • 1-3 years of experience working in a cGMP-regulated pharmaceutical, biotechnology, or life sciences laboratory environment preferred.
  • Knowledge of laboratory analytical techniques, quality systems, data integrity principles, and regulatory requirements.
  • Strong organizational skills with the ability to manage multiple priorities and meet deadlines.
  • Excellent attention to detail, documentation practices, and problem-solving abilities.
  • Effective communication and teamwork skills with the ability to work cross-functionally.
  • Proficiency with laboratory documentation systems and Microsoft Office applications.

Note: This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
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