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Quality Control Pharma 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 ...

Jubilant Pharma, LLC

Manager, QC - Weekend

Spokane, WA · On-site

$102 - $136/hr

Jubilant HollisterStier is proudly part of the global, Jubilant Pharma family. established force in ... The position of Weekend Quality Control (QC) Manager is responsible for providing cross-functional ...

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 ...

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

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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 ...

Catalent, Inc.

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

Jubilant Pharma, LLC

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 ...

Bachem

Quality Control Project Manager

Vista, CA · On-site

$98K - $135K/yr

Bachelor's degree in chemistry or a related life sciences field * 5+ years' QC experience in biotech/pharma * 3+ years' experience in a biotech/pharma CDMO setting * 4+ years of project management ...

ThompsonFirstGroup

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 ...

Jubilant Pharma, LLC

$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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Quality Control Pharma information

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How much do quality control pharma jobs pay per hour?

As of Sep 7, 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 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 are the key skills and qualifications needed to thrive as a quality control professional in the pharmaceutical industry?

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 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.

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.

Is Quality Control Pharma a good career?

Quality Control Pharma involves testing and inspecting pharmaceutical products to ensure they meet safety and quality standards. It requires attention to detail, knowledge of laboratory techniques, and often involves certifications such as GMP training. The role offers stable employment opportunities in the pharmaceutical industry with potential for career advancement.
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Quality Control Pharma jobs near you
Infographic showing various Quality Control Pharma job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $43,612 per year, or $21 per hour.

QC Analyst (Pharma)

Astrix Inc

Ventura, CA • On-site

$39 - $41/hr

Full-time, Contractor

Re-posted 21 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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