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Temp Pharma Quality Assurance Jobs (NOW HIRING)

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QA Associate

Quakertown, PA · On-site

$900 - $1.4K/wk

Previous experience in a regulated manufacturing environment (food or pharma), quality assurance, or other related fields * Knowledge of Good Manufacturing Practices (GMP) * Familiarity with ...

Careers at RK Pharma Inc.

QA Associate

Pearl River, NY · On-site

$55K - $95K/yr

About RK Pharma RK Pharma is a pharmaceutical organization dedicated to delivering high-quality ... About the Role The QA Associate supports production-related quality activities to ensure processes ...

Atilar Pharma

QA Supervisor

Houston, TX · On-site

$70 - $90/hr

Atilar Pharma specializes in the production of high-quality compounded medications for healthcare ... The QA Supervisor will be responsible for overseeing all aspects of the company's quality assurance ...

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How much do temp pharma quality assurance jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for temp pharma quality assurance in the United States is $23.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $24.28 per hour, depending on experience, location, and employer.

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

AspectTemp Pharma Quality AssuranceTemp Pharma Quality Control
Primary FocusEnsuring processes meet quality standards and regulatory requirementsTesting and inspecting products to verify quality and compliance
ResponsibilitiesDeveloping protocols, audits, process validationSampling, laboratory testing, data analysis
Work EnvironmentDocumentation, audits, process oversightLaboratories, testing facilities
CertificationsGMP, QA certifications often preferredGMP, laboratory testing certifications

Temp Pharma Quality Assurance focuses on maintaining quality systems and compliance, while Temp Pharma Quality Control emphasizes testing and verifying product quality. Both roles are essential in the pharmaceutical industry but serve different functions within the quality management process.

How to get into Temp Pharma Quality Assurance?

To enter a Temp Pharma Quality Assurance role, candidates typically need a background in life sciences, pharmacy, or related fields, along with knowledge of Good Manufacturing Practices (GMP) and quality control procedures. Relevant certifications such as CQE or GMP training can improve prospects, and prior experience in pharmaceutical or manufacturing environments is often preferred. Strong attention to detail, analytical skills, and familiarity with documentation and compliance standards are essential for success in this role.

Is Temp Pharma Quality Assurance a good career?

A career in pharmaceutical quality assurance involves ensuring compliance with industry standards and regulations, often requiring attention to detail and knowledge of Good Manufacturing Practices (GMP). It offers stable employment opportunities, potential for advancement, and the chance to work in a regulated environment focused on product safety. Certifications such as CQE or GMP training can enhance job prospects in this field.
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Temp Pharma Quality Assurance jobs near you
Infographic showing various Temp Pharma Quality Assurance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $48,237 per year, or $23.2 per hour.

Quality Assurance Supervisor

Garonit Pharmaceutical

Flanders, NJ • On-site

Full-time

Posted 13 days ago

Job description

Quality Assurance Supervisor
Onsite in Flanders, NJ
We're looking for a Quality Assurance Supervisor who's hands-on, meticulous, and passionate about setting up quality systems. You'll play a key role in developing and implementing our Quality Management System (QMS), preparing for pre-approval inspections, and supporting new product development.
What You'll Do
  • Develop, implement, and maintain the Quality Management System (QMS).
  • Drive the transition from paper-based to electronic systems (LIMS, TrackWise).
  • Conduct internal audits and ensure inspection readiness (PAI, regulatory).
  • Ensure compliance with cGMP and industry standards.
  • Review and approve SOPs, batch records, deviations, and change controls.
  • Analyze quality data to identify trends and drive continuous improvement.
  • Develop and implement Corrective and Preventive Actions (CAPA).
  • Coordinate with other departments to resolve quality issues quickly and effectively.
  • Prepare and present quality performance reports to management.
  • Train and mentor QA staff to build a culture of quality and excellence.

What You'll Bring
  • Bachelor's degree in related field
  • 3-5 years of experience in pharma QA supporting drug product development and manufacturing.
  • Proven experience in establishing or managing Quality Systems and preparing for audits/inspections.
  • Strong understanding of GMP, QMS, and ISO 9001 standards.
  • Hands-on experience with LIMS, TrackWise, or other eQMS tools.
  • Excellent leadership, communication, and problem-solving skills.
  • Highly meticulous, data-driven, and comfortable in a fast-paced, startup-like environment.

Why Garonit Pharma
  • Be part of a core leadership team with exciting growth plans for the future.
  • Shape a modern, digital-first Quality Management System.
  • Collaborate with experienced professionals passionate about quality and innovation.
  • Competitive compensation and long-term career growth opportunities.

Apply