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Pharmaceutical Quality Assurance Associate Jobs (NOW HIRING)

CEDENT

Quality Assurance Associate I

Cumberland, RI · On-site

... pharmaceutical regulatory requirements: FDA, GMP. Provides QA oversight to operations under ... The QA Associate II/III independently conducts quality assurance audits of production records ...

INCOG

QA Associate, 2nd Shift

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 ...

Avcend

Quality Assurance Associate

Reno, NV · On-site

$28.40/hr

Quality Assurance Associate Payrate: $28.85 / hr. on W2 Work Week   1 - Monday, 2 - Tuesday, 3 - Wednesday, 4 - Thursday, 5 - Friday Job Description/Comment: Responsible for all activities ...

Actalent

Quality Assurance Associate

Centerbrook, CT

Quality Assurance Associate The Quality Assurance Associate assists in the management, administration, and maintenance of the Quality System to ensure compliance with internal standards and external ...

New

TEK Systems

Quality Assurance Associate

Hanover, MD · On-site

$21.63/hr

The QA Associate is experienced in day-to-day process (payroll and billing) issues, operational policies and procedures, and the PeopleSoft system as it pertains to such processes. Qualities include ...

HelloFresh

Quality Assurance Associate

Aurora, IL · On-site

$20.75/hr

The Quality Assurance Associate audits our production processes to ensure our customers receive a safe, high-quality product. This position completes various inspections on the quality of fresh ...

INCOG

QA Associate, 3rd Shift

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 ...

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

As of Aug 7, 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 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $60,925 per year, or $29.3 per hour.

Quality Assurance Associate I

CEDENT

Cumberland, RI • On-site

Full-time

Re-posted 16 days ago

Job description

SUMMARY/OBJECTIVE
This position supports activities of the Quality Assurance Department regarding pharmaceutical manufacturing, testing and packaging to ensure compliance with all relevant pharmaceutical regulatory requirements: FDA, GMP. Provides QA oversight to operations under direction of the QA Manager. Provides review, impact/risk assessment analysis, detailed improvement plans for change controls, deviations, investigations and CAPA. Adheres to Client compliance initiatives, including
following all quality and division/company policy requirements. Helps to ensure that all Client products meet quality requirements by supporting all assigned quality aspects of product approval. The QA Associate II/III independently conducts quality assurance audits of production records (manufacturing, analytical and quality control records) and facility records assuring company standards are maintained and product integrity is preserved.
RESPONSIBILITIES
1. Provide support to GMP investigations, validation documentation review and approval, identify gaps within existing Quality Systems and propose solutions for functional management;
2. Participates/leads internal/external audits, prepare and issue audit reports. Recommend remediation actions and follow up on implementation of the plan.
3. Supports resolution of technical and compliance issues/gap analysis.
4. Aides implementation of Quality Systems/System Improvements.
5. Supports and assists with Quality systems-related training, including compliance with cGMP and SOPs.
6. Interface with key quality, manufacturing, customers and coordinate documentation impacting quality areas.
7. Review/approval of all cGMP documents generated across site to include (but not limited to): SOPs, technical reports, validation documents, QA assessment, APRs, audit documents, change control, deviation & document revisions, etc.
8. Participates in activities associated with primary batch record review, non-conformances investigation and CAPA.
9. Work in coordination with regulatory affairs group in support of ANDA submissions.
10. Provides QA review/approval of all cGMP documents associated with manufacture of product.
11. Communicates with contractors and internal manufacturing/technical groups regarding compliance and quality issues (i.e., batch documentation, investigations, timelines and data related issues).
12. Authors or revises SOPs as necessary.
13. Actively engaged in the training of staff with lesser experience or knowledge of quality assurance processes. Educate and instruct QA and plant personnel in quality best practices for sampling, labeling,
good documentation practices, equipment sanitation. Confirm these procedures are being adhered to, taking corrective actions when non-conformances are observed.
14. Routinely provide input to quality and operations management for better operational procedures to improve overall efficiency and regulatory compliance.
15. Assist in development of special department projects and work in conjunction with quality management.
16. Other duties as assigned.
COMPETENCIES
1. Project Management
2. Technical Capacity.
3. Discretion.
4. Problem Solving/Analysis.
5. Decision Making.
6. Communication Proficiency.
7. Collaboration Skills.
8. Learning Agility
9. Managing Changing Priorities
POSITION TYPE/EXPECTED HOURS OF WORK
This is a full-time position requiring 40 or more hours of work per week.
 
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About Cedent

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CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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