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Pharma Qc Jobs (NOW HIRING)

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 ...

Techtrueup

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 ...

Techtrueup

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 ...

System One

Quality Control - GMP Pharma

Allentown, PA · On-site

$20.25/hr

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 ...

Techtrueup

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 ...

LGM Pharma, LLC

QC CHEMIST III

Irvine, CA · On-site

$34 - $38/hr

We have an open QC CHEMIST III position in our Quality Control Department in the Irvine, CA ... At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity ...

Piramal Pharma Limited

QC Analyst II

Sellersville, PA · On-site

$23.25 - $31.25/hr

Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract ... For more details, please visit : www.piramalpharmasolutions.com Job Title QC Analyst II The ...

Intellectt INC

QC Analyst

Lebanon, IN · On-site

$23 - $31/hr

Develop/revise worksheets and system documentation Required Skills: * 8-10 years in Pharma/GMP environment * QC lab experience with LIMS/ELN (data admin or power user) * Strong understanding of data ...

Garonit Pharmaceutical

QC Supervisor

Fairfield, NJ · On-site

QC Supervisor Onsite in Fairfield, NJ We're looking for a QC Supervisor who's both a hands-on ... Why Garonit Pharma * Work with cutting-edge equipment in a collaborative, growth-oriented ...

Piramal Pharma Limited

QC Analyst II

Sellersville, PA · On-site

$23.25 - $31.25/hr

Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract ... For more details, please visit : www.piramalpharmasolutions.com Job Title QC Analyst II The ...

Astrix Inc

QC Lab Associate

Newark, CA · On-site

$28 - $31/hr

... pharma environment. Location : Newark, CA (on-site) | 1-year contract | Shift : M-F 9-5 | ... Good communication skills * QC experience is a plus * Basic computer skills (Word, Excel, Outlook)

Körber Pharma Packaging Materials US

Be Seen First

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 ...

LabPersonnel

Be Seen First

Quality Control Technician

Elgin, IL · On-site

$50K/yr

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 ...

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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 13, 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 1% As Needed, 93% Full Time, 2% Part Time, 1% Temporary, and 3% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $58,065 per year, or $27.9 per hour.
QC Analyst (Pharma)

QC Analyst (Pharma)

Astrix Inc

Ventura, CA • On-site

$39 - $41/hr

Full-time, Contractor

Posted 25 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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