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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
Join us and transform the lives of patients while transforming your career. Sr Associate QA What you will do Let's do this. Let's change the world. In this vital role you will be responsible for ...
Join us and transform the lives of patients while transforming your career. Sr Associate QA What you will do Let's do this. Let's change the world. In this vital role you will be responsible for ...
Quality Assurance Subcategory: Qual Assurance Schedule: Full-Time Shift: Day Job Travel: Yes - 10% of the time Minimum Clearance Required: Interim_Secret Clearance Level Must Be Able to Obtain:
Quality Assurance Subcategory: Qual Assurance Schedule: Full-Time Shift: Day Job Travel: Yes - 10% of the time Minimum Clearance Required: Interim_Secret Clearance Level Must Be Able to Obtain:
Description SAIC is seeking a Quality Assurance Supervisor in Middletown, RI. This role is responsible for overseeing the QA / QC team and ensuring the organization's products, services, and ...
Description SAIC is seeking a Quality Assurance Supervisor in Middletown, RI. This role is responsible for overseeing the QA / QC team and ensuring the organization's products, services, and ...
Description SAIC is seeking a Quality Assurance Supervisor in Middletown, RI. This role is responsible for overseeing the QA / QC team and ensuring the organization's products, services, and ...
Description SAIC is seeking a Quality Assurance Supervisor in Middletown, RI. This role is responsible for overseeing the QA / QC team and ensuring the organization's products, services, and ...
SAIC is seeking a Quality Assurance Supervisor in Middletown, RI. This role is responsible for overseeing the QA / QC team and ensuring the organization's products, services, and processes meet the ...
SAIC is seeking a Quality Assurance Supervisor in Middletown, RI. This role is responsible for overseeing the QA / QC team and ensuring the organization's products, services, and processes meet the ...
SAIC is seeking a Quality Assurance Supervisor in Middletown, RI. This role is responsible for overseeing the QA / QC team and ensuring the organization's products, services, and processes meet the ...
SAIC is seeking a Quality Assurance Supervisor in Middletown, RI. This role is responsible for overseeing the QA / QC team and ensuring the organization's products, services, and processes meet the ...
Quality Assurance Manager
Newport, RI · On-site
$92K - $166K/yr
The Quality Assurance Manager will: * Provide Towed Array Depot Quality Assurance oversight and direction to a team of inspectors. * Monitor operation's adherence to NATSC processes and procedures ...
New
Quality Assurance Manager
Newport, RI · On-site
$92K - $166K/yr
The Quality Assurance Manager will: * Provide Towed Array Depot Quality Assurance oversight and direction to a team of inspectors. * Monitor operation's adherence to NATSC processes and procedures ...
New
Quality Assurance Analyst
Carolina, RI · On-site +1
$55K - $65K/yr
Primary Functions Reporting to the Mobile Team Lead, the Quality Assurance Analyst's key responsibilities will include: * Create, maintain, and execute test plans, test cases, and test scripts for ...
Quality Assurance Analyst
Carolina, RI · On-site +1
$55K - $65K/yr
Primary Functions Reporting to the Mobile Team Lead, the Quality Assurance Analyst's key responsibilities will include: * Create, maintain, and execute test plans, test cases, and test scripts for ...
In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of Manufacturing activities. This position requires working directly with Manufacturing staff during ...
In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of Manufacturing activities. This position requires working directly with Manufacturing staff during ...
Senior Salesforce QA Analyst
Providence, RI · On-site
$94 - $140/hr
We believe in equipping our associates with the knowledge and resources they need to be successful ... Lead QA planning and execution across agile ceremonies, including backlog refinement, sprint ...
Senior Salesforce QA Analyst
Providence, RI · On-site
$94 - $140/hr
We believe in equipping our associates with the knowledge and resources they need to be successful ... Lead QA planning and execution across agile ceremonies, including backlog refinement, sprint ...
The Manager, Quality Assurance TCR oversees quality assurance and operational excellence initiatives at the Taco Cranston (TCR) facility, aligning them with organizational goals and business ...
New
The Manager, Quality Assurance TCR oversees quality assurance and operational excellence initiatives at the Taco Cranston (TCR) facility, aligning them with organizational goals and business ...
New
The Manager, Quality Assurance TCR oversees quality assurance and operational excellence initiatives at the Taco Cranston (TCR) facility, aligning them with organizational goals and business ...
New
The Manager, Quality Assurance TCR oversees quality assurance and operational excellence initiatives at the Taco Cranston (TCR) facility, aligning them with organizational goals and business ...
New
We believe in equipping our associates with the knowledge and resources they need to be successful ... Lead QA planning and execution across agile ceremonies, including backlog refinement, sprint ...
We believe in equipping our associates with the knowledge and resources they need to be successful ... Lead QA planning and execution across agile ceremonies, including backlog refinement, sprint ...
Senior Salesforce QA Analyst
Providence, RI · On-site +1
$93K - $140K/yr
We believe in equipping our associates with the knowledge and resources they need to be successful ... Lead QA planning and execution across agile ceremonies, including backlog refinement, sprint ...
Senior Salesforce QA Analyst
Providence, RI · On-site +1
$93K - $140K/yr
We believe in equipping our associates with the knowledge and resources they need to be successful ... Lead QA planning and execution across agile ceremonies, including backlog refinement, sprint ...
QA/Test Engineer
Middletown, RI · On-site
$41 - $56/hr
Responsibilities This position requires a Quality Assurance QA/Test Engineer with Software QA/Test experience. Tasks include, but are not limited to, software testing and quality assurance for ...
QA/Test Engineer
Middletown, RI · On-site
$41 - $56/hr
Responsibilities This position requires a Quality Assurance QA/Test Engineer with Software QA/Test experience. Tasks include, but are not limited to, software testing and quality assurance for ...
Acute Care TechnologyThis position is responsible for developing, implementing and managing quality assurance and quality control program designed to ensure continuous production of electrodes ...
Acute Care TechnologyThis position is responsible for developing, implementing and managing quality assurance and quality control program designed to ensure continuous production of electrodes ...
Quality Assurance support of all programs at the Depot, Hose/Tow Cable fabrication/repair shops and QA Receiving. * Evaluation/Inspection of work performed in accordance with Government generated ...
Quality Assurance support of all programs at the Depot, Hose/Tow Cable fabrication/repair shops and QA Receiving. * Evaluation/Inspection of work performed in accordance with Government generated ...
Quality Assurance Associate information
See Rhode Island salary details
$12.71 - $17.08
17% of jobs
$18.52 is the 25th percentile. Wages below this are outliers.
$17.08 - $21.44
24% of jobs
The median wage is $23.63 / hr.
$21.44 - $25.81
18% of jobs
$25.81 - $30.18
15% of jobs
$30.54 is the 75th percentile. Wages above this are outliers.
$30.18 - $34.54
10% of jobs
$34.54 - $38.91
8% of jobs
$38.91 - $43.27
5% of jobs
$43.27 - $47.64
3% of jobs
$47.64 - $52
0% of jobs
$52 - $56.37
0% of jobs
$56.37 - $60.74
0% of jobs
$12
$28
$60
How much do quality assurance associate jobs pay per hour?
As of Aug 30, 2026, the average hourly pay for quality assurance associate in Rhode Island is $28.68, according to ZipRecruiter salary data. Most workers in this role earn between $18.37 and $33.65 per hour, depending on experience, location, and employer.
What does a quality assurance associate do?
A Quality Assurance Associate is responsible for monitoring and evaluating the various processes involved in product development and production to ensure they meet established quality standards. Their duties typically include conducting inspections, documenting findings, assisting in process improvements, and ensuring compliance with regulatory requirements. They play a critical role in identifying defects, reducing errors, and maintaining the overall quality of products or services before they reach customers.
What skills and qualifications are needed to be a quality assurance associate?
To excel as a Quality Assurance Associate, you need a solid understanding of quality control principles, attention to detail, and often a degree in a related field like chemistry, biology, or engineering. Familiarity with industry-standard quality management systems (such as ISO 9001), statistical analysis software, and documentation tools is typically required. Strong problem-solving skills, effective communication, and the ability to work collaboratively are highly valued in this role. These skills ensure that products and processes consistently meet standards, reduce errors, and maintain compliance with regulatory requirements.
What are common challenges faced by quality assurance associates in ensuring consistent product quality?
Quality Assurance Associates often encounter challenges such as managing tight production deadlines while maintaining thorough testing standards, addressing unexpected defects, and adapting quickly to new regulatory or product requirements. Effective communication with production, development, and regulatory teams is crucial for resolving issues efficiently. Staying current with evolving quality standards and continuously improving testing processes are also important for success in this role.
What is the difference between Quality Assurance Associate vs Quality Control Inspector?
| Aspect | Quality Assurance Associate | Quality Control Inspector |
|---|---|---|
| Certifications | Often requires certifications like ASQ CQIA or related quality assurance training | May require certifications such as ISO auditor or specific industry standards |
| Work Environment | Involves process audits, documentation, and improving quality systems | Focuses on inspecting products or materials for defects |
| Employer & Industry Usage | Common in manufacturing, pharmaceuticals, and tech industries | Primarily in manufacturing, food production, and assembly lines |
While both roles focus on quality, the Quality Assurance Associate emphasizes developing and maintaining quality systems and processes, whereas the Quality Control Inspector concentrates on inspecting products for defects. Both roles are essential for ensuring product quality but differ in scope and responsibilities.
Is a Quality Assurance Associate an entry-level job?
A Quality Assurance Associate position is often considered entry-level, suitable for candidates with little to no prior experience in quality assurance or related fields. It typically requires basic knowledge of testing procedures, attention to detail, and may involve training on specific tools or software used in quality control processes.
What is the role of a quality assurance associate?
A quality assurance associate is responsible for monitoring and testing products or services to ensure they meet quality standards and specifications. They often develop testing procedures, document issues, and collaborate with teams to improve processes, using tools like checklists and quality management systems. Attention to detail and knowledge of industry regulations are essential for this role.
What are the most commonly searched types of Quality Assurance jobs in Rhode Island?
The most popular types of Quality Assurance jobs in Rhode Island are:
What are popular job titles related to Quality Assurance Associate jobs in Rhode Island?
For Quality Assurance Associate jobs in Rhode Island, the most frequently searched job titles are:
What job categories do people searching Quality Assurance Associate jobs in Rhode Island look for?
The top searched job categories for Quality Assurance Associate jobs in Rhode Island are:
What cities in Rhode Island are hiring for Quality Assurance Associate jobs?
Cities in Rhode Island with the most Quality Assurance Associate job openings:
Quality Assurance Associate I
Cumberland, RI • On-site
CEDENT •
IT Services • 11 - 50 employees11 - 50 employees
Full-time
Re-posted 9 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.
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.
About Cedent
Sourced by ZipRecruiter
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