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Pharmaceutical Quality Assurance

Sylmar, CA · On-site

$25 - $30/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

A pharmaceutical Quality Assurance (QA) professional ensures that drug products are safe, effective, and compliant with regulatory standards. They proactively design systems to prevent defects ...

INCOG BioPharma Services

QA Associate

Fishers, IN · On-site

Working closely with the QA Supervisor, the QA Associate will be instrumental in ensuring site ... Pharmaceutical Manufacturing environment. * Moderate knowledge of regulations and quality systems ...

INCOG BioPharma Services

QA Associate

Fishers, IN · On-site

Working closely with the QA Supervisor, the QA Associate will be instrumental in ensuring site ... Pharmaceutical Manufacturing environment. * Moderate knowledge of regulations and quality systems ...

INCOG

QA Associate

Fishers, IN · On-site

The QA Associate will need to provide support with identifying operational and quality gaps. The ... Pharmaceutical Manufacturing environment. * Moderate knowledge of regulations and quality systems ...

Discovery Life Sciences

Quality Assurance Associate

Newtown, PA · On-site

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The QA Associate will also be providing local internal and external audit support at our Newtown ... Bachelor's degree in Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, Life Sciences, or a ...

INCOG BioPharma Services

QA Associate

Fishers, IN · On-site

The QA Associate will need to provide support with identifying operational and quality gaps. The ... Pharmaceutical Manufacturing environment. * Moderate knowledge of regulations and quality systems ...

Reva Medical LLC

Quality Assurance Associate

San Diego, CA · On-site

$24 - $33/hr

Quality Assurance Associate - Document Control, Training, and Asset ManagementJob PurposeThe ... Medical device or pharmaceutical experience is desirable.Basic knowledge of, or ability to learn ...

Posted today

Lancesoft

QA Associate

Winchester, KY · On-site

$24 - $26.38/hr

... pharmaceutical products. Perform routine testing of in-process and finished product samples ... Quality Assurance Associate Bachelors degree;OR Associates with 1 year of related work experience;

Lancesoft

Quality Assurance Associate

Winchester, KY · On-site

$24 - $26.38/hr

... pharmaceutical products. Perform routine testing of in-process and finished product samples ... Quality Assurance Associate Bachelors degree;OR Associates with 1 year of related work experience;

Astrix Inc

QA Associate (Part Time)

Kalamazoo, MI · On-site

$19 - $20/hr

... pharmaceutical manufacturing team on a part-time basis. This role is ideal for recent graduates or individuals with 0-2 years of experience in a GMP-regulated environment. The QA Associate will ...

ConnectiveRx

QA Associate

Pittsburgh, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

When things get messy along the prescription journey, pharmaceutical manufacturers rely on us to ... The Operations Quality Assurance Associate I serves as a subject matter expert for assigned ...

Actalent

QA Associate

Clinton, IN

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Title: QA Associate The QA Associate supports the review and analysis of data related to ... Demonstrated experience working in a GMP, pharmaceutical, life science, or highly regulated quality ...

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All JobsPharmaceutical Quality Assurance Associate Jobs

Pharmaceutical Quality Assurance Associate information

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$12

$29

$62

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

As of Aug 12, 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 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 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 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.

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.
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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, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $60,925 per year, or $29.3 per hour.

Quality Assurance Associate

StaffManagement

Bridgewater, NJ • On-site

$28 - $31/hr

Full-time

Posted 5 days ago

Job description

Staff Management Group is seeking a Quality Assurance Associate for our client in Bridgewater, NJ. Please read the ENTIRE job description and ALL of the job requirements BEFORE applying for this position.

Schedule

  • 1st shift: 9AM - 5PM

Pay Rate

  • $28 - $31 / hour

Job Summary

We are seeking a detail-oriented and motivated Quality Assurance Associate to support pharmaceutical quality operations and ensure products and documentation meet established quality and regulatory requirements.


This role assists with batch release activities, product complaints, recalls and field alerts, quality agreements, deviations, investigations, and SOP management. The Quality Assurance Associate will also coordinate with manufacturing sites, corporate Quality Assurance, contract testing laboratories, and third-party logistics providers to support testing and quality-related activities.


The ideal candidate is highly organized, accurate, and able to manage multiple priorities in a fast-paced pharmaceutical environment while maintaining strong attention to detail and clear communication.

Job Responsibilities:

  • With Supervision, review documents/records and provide batch release authorization to 3PL service provider for products manufactured outside of the US
  • Support Drug Product Complaint management; forwarding to respective drug product manufacturing site and coordinate with corporate QA for investigations.
  • Support Drug Product recall/field alert management.
  • Assist with review of Quality Agreements
  • For applicable products, coordinate with Contract Testing Laboratories for Analytical Method Transfer activities, Drug Product testing, any OOS results, and test method issues.
  • With supervision, review deviations/investigations related to Strides Pharma Inc (Strides) frontend products.
  • Assist with SOP management for Strides’ US corporate office.

Job Requirements

  • Bachelor’s degree in pharmacy, Chemistry, Biology or Microbiology is preferred
  • 3 years of Quality Assurance or related pharmaceutical industry experience is preferred.
  • Recent graduates will be considered for this role.
  • Excellent verbal and written communication skills are a MUST.
  • With supervision and direction, effectively prioritizes competing tasks in a fast-paced and dynamic environment
  • Motivated, results driven with attention to detail, accuracy and clarity.
  • Candidate should be a self-starter, highly motivated and very detailed oriented.

Additional Information

Staff Management Group is an equal employment opportunity employer, and all qualified applicants will receive consideration for employment without unlawful discrimination based on race, color, creed, national origin, sex, age, disability, marital status, sexual orientation, or citizenship status.

About Staff Management Group: Staff Management Group has over 30 years of experience placing staffing candidates in distribution, manufacturing, production, assembly, and clerical positions. Staff Management Group is one of New Jersey’s leading staffing and recruiting agencies specializing in light industrial and clerical staffing. Come join the team!

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