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Pharmaceutical Quality Assurance

Sylmar, CA · On-site

$25 - $30/hr

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

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

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 ...

INCOG BioPharma Services

QA Associate

Fishers, IN

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

INCOG BioPharma Services

QA Associate

Fishers, IN · On-site

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

Cipla

QA Associate IT

Fall River, MA · On-site

$76K - $103K/yr

The IT- QA Associate position is an individual contributor role and a member of the InvaGen Pharmaceuticals Quality Team. The position monitors changes to electronic records, alterations in critical ...

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;

Actalent

QA Associate

Bridgeton, MO

$24/hr

The QA Associate works independently on smaller projects, collaborates closely with cross ... Experience working in or with pharmaceutical environments, strongly preferred. * High level of ...

Actalent

QA Associate

Bridgeton, MO

$24/hr

The QA Associate works independently on smaller projects, collaborates closely with cross ... Experience working in or with pharmaceutical environments, strongly preferred. * High level of ...

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;

ConnectiveRx

QA Associate

Pittsburgh, PA · On-site

$18.98 - $25.85/hr

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 ...

ConnectiveRx

QA Associate

Pittsburgh, PA

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 ...

ConnectiveRx

QA Associate

Pittsburgh, PA

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 ...

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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 Jul 27, 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, and why are they important?

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 July 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $60,925 per year, or $29.3 per hour.
Quality Assurance Associate

Quality Assurance Associate

Garonit Pharmaceutical

Fairfield, NJ • On-site

Full-time

Posted 28 days ago

Job description

QA Associate
Onsite in Flanders, NJ and Fairfield, NJ
Garonit Pharma is seeking a detail-oriented and collaborative QA Associate to support daily Quality Assurance operations and uphold our Quality Management System. This role is essential in ensuring product quality, cGMP compliance, and smooth operational support across manufacturing and warehouse functions.
What You'll Be Doing:
  • Issue, review, and maintain batch records
  • Prepare and review documentation for Operations
  • Review Certificates of Analysis (COAs)
  • Track material status and maintain data integrity
  • Author, revise, and manage SOPs and controlled documents
  • Write investigations, change controls, and implement CAPAs
  • Conduct employee training
  • Support internal, customer, and regulatory audits
  • Compile data for Annual Product Reviews (APRs)
  • Schedule calibration and certification activities
  • Respond to customer requests and questionnaires
  • Track vendor qualifications
  • Perform data entry, collection, and documentation review
  • Review shipment inspection forms
  • Assist with other QA duties as assigned

What You Bring:
  • Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or a related scientific discipline preferred
  • Minimum 1-3 years of experience in a regulated cGMP pharmaceutical manufacturing environment
  • FDA-regulated industry experience
  • Experience supporting QC systems and auditing laboratory documentation/data is strongly preferred
  • Experience with Empower software is preferred
  • Working knowledge of 21 CFR Parts 210/211 and ICH guidelines
  • Strong understanding of cGMP and Quality Management Systems
  • Experience reviewing laboratory documentation, analytical data, and quality records
  • Excellent documentation accuracy and attention to detail
  • Strong organizational, written, and verbal communication skills
  • Proficiency in Microsoft Word and Excel
  • Ability to multitask in a fast-paced environment
  • Strong interpersonal skills with the ability to work independently and collaboratively across departments

Apply