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Pharmaceutical Quality Assurance Associate Jobs (NOW HIRING)

Astrix Inc

QA Associate (Part Time)

Kalamazoo, MI · On-site

$19 - $20/hr

Pay Rate Low: 19 | Pay Rate High: 20 Position: Entry-Level Quality Assurance Associate (Part-Time) ... active pharmaceutical ingredients for human use are in compliance with established company ...

Socket.dev

Pharmaceutical QA Director

Tustin, CA · On-site

$180 - $260/hr

The Pharmaceutical QA Director plays a critical leadership role in ensuring the highest standards of quality and compliance within pharmaceutical manufacturing operations. This position is ...

Lancesoft INC

Quality Assurance Associate

Winchester, KY · On-site

$24 - $26/hr

Quality Assurance Associate Location: Winchester, KY 40391 TEMP TO HIRE - DURATION - 6 MONTHS ... pharmaceutical products. * Perform routine testing of in-process and finished product samples ...

Reva Medical LLC

Quality Assurance Associate

San Diego, CA · On-site

$24 - $33/hr

Quality Assurance Associate - Document Control, Training, and Asset Management Job Purpose The ... Medical device or pharmaceutical experience is desirable. * Basic knowledge of, or ability to learn ...

Bimeda Inc.

Quality Assurance Associate

Le Sueur, MN · On-site

$26 - $30/hr

The QA Associate will be directly involved in all areas of quality assurance, including change ... Minimum 1+ years of direct work experience with pharmaceutical or food manufacturing Quality ...

ANI Pharmaceuticals

QA Associate

East Windsor, NJ · On-site

$52K - $70K/yr

About Us Welcome to ANI Pharmaceuticals, where we are dedicated to improving and enhancing patients ... in Quality Assurance Minimum Field of Expertise • Computer skills • Previous work in a ...

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Pharmaceutical Quality Assurance Associate information

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How much do pharmaceutical quality assurance associate jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for pharmaceutical quality assurance associate in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.

What does a pharmaceutical quality assurance associate do?

A Pharmaceutical Quality Assurance (QA) Associate is responsible for ensuring that pharmaceutical products are produced and controlled according to quality standards and regulatory requirements. They review documentation, monitor manufacturing processes, conduct audits, and help investigate deviations to ensure compliance with Good Manufacturing Practices (GMP). By maintaining strict quality control, QA Associates play a key role in protecting patient safety and ensuring that medications are safe and effective.

What are the key skills and qualifications needed to thrive as a pharmaceutical quality assurance associate?

To thrive as a Pharmaceutical Quality Assurance Associate, you need a bachelor's degree in pharmacy, chemistry, or a related field, with a thorough understanding of GMP regulations and quality control processes. Familiarity with quality management systems (QMS), documentation software, and regulatory compliance tools is typically required. Strong attention to detail, effective communication, and problem-solving abilities are crucial soft skills for this role. These competencies are vital to ensure product safety, regulatory compliance, and the consistent delivery of high-quality pharmaceuticals.

What are the typical challenges faced by a pharmaceutical quality assurance associate when maintaining compliance in a dynamic production environment?

Pharmaceutical Quality Assurance Associates often encounter challenges such as keeping up with frequent changes in regulatory requirements, coordinating with cross-functional teams to ensure documentation accuracy, and responding promptly to deviations or non-conformances. The fast-paced nature of pharmaceutical production means you must be detail-oriented while managing multiple tasks and deadlines. Collaborating closely with production, R&D, and regulatory teams is essential to ensure products meet all quality and safety standards, which can require strong communication and problem-solving skills.

What is the difference between Pharmaceutical Quality Assurance Associate vs Pharmaceutical Quality Control Analyst?

AspectPharmaceutical Quality Assurance AssociatePharmaceutical Quality Control Analyst
Primary FocusEnsuring compliance with quality standards, reviewing documentation, and auditing processesTesting and analyzing drug products to verify quality and safety
Required CredentialsBachelor's degree in life sciences or related field, GMP trainingBachelor's degree in chemistry, biology, or related field, lab certifications
Work EnvironmentOffice-based, quality departments, audits, documentation reviewLaboratory setting, performing tests and analyses
Employer & Industry UsagePharmaceutical companies, biotech firms, regulatory agenciesPharmaceutical manufacturing, biotech labs, quality testing facilities

While both roles support pharmaceutical quality, the Pharmaceutical Quality Assurance Associate focuses on compliance, documentation, and process audits, whereas the Pharmaceutical Quality Control Analyst concentrates on laboratory testing and product analysis. Both are essential for ensuring drug safety and quality but serve different functions within the industry.

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Pharmaceutical Quality Assurance Associate jobs near you
Infographic showing various Pharmaceutical Quality Assurance Associate 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 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $60,925 per year, or $29.3 per hour.

QA Associate (Part Time)

Astrix Inc

Kalamazoo, MI • On-site

$19 - $20/hr

Part-time

Re-posted 22 days ago

Job description

Pay Rate Low: 19 | Pay Rate High: 20
Position: Entry-Level Quality Assurance Associate (Part-Time)
Location: Kalamazoo, MI
Pay Rate: $19-20/hour
Schedule: Part-time, 4-5 hours per day
Position Summary
Responsible for supporting the Quality Assurance group in maintaining the Quality Management Systems. This role ensures that manufacturing and QC activities for the production and testing of active pharmaceutical ingredients for human use are in compliance with established company procedures and applicable GMP and ICH regulations.
Duties and Responsibilities
  • Review laboratory records for raw materials and disposition raw materials in accordance with approved procedures
  • Coordinate and prepare records for off-site storage, including inventory documentation and shipment to Iron Mountain
  • Support data collection and compilation activities for campaign reporting
  • Support the Quality Assurance group in maintaining Quality Management Systems
  • Assist the Quality Assurance group in ensuring site compliance with cGMPs and ICH guidelines at all times, and support site inspection readiness

Minimum Qualifications, Skills, and Requirements
  • Associate's degree in a science-related field or equivalent experience; Bachelor's degree in Biology, Biochemistry, or Chemistry preferred
  • 0-3 years' experience in a pharmaceutical quality environment (quality control and/or quality assurance)
  • Working knowledge of cGMP, ICH, and industry best practices preferred
  • Experience with clinical and commercial cGMP requirements preferred
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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