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 ...
Sr Associate QA - Nights
West Greenwich, RI · On-site
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 ...
Sr Associate QA - Nights
West Greenwich, RI · On-site
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 Supervisor
Middletown, RI · On-site
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 Supervisor
Middletown, RI · On-site
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 Supervisor
Middletown, RI · On-site
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 ...
Quality Assurance Supervisor
Middletown, RI · On-site
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 ...
Quality Assurance Supervisor
Middletown, RI · On-site
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 ...
Quality Assurance Supervisor
Middletown, RI · On-site
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 ...
Quality Assurance Supervisor
Middletown, RI · On-site
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 Supervisor
Middletown, RI · On-site
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 Supervisor
Middletown, RI · On-site
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 Supervisor
Middletown, RI · On-site
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 ...
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 ...
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 ...
Manager, Quality Assurance TCR
Cranston, RI · On-site
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 ...
Manager, Quality Assurance TCR
Cranston, RI · On-site
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 ...
Manager, Quality Assurance TCR
Cranston, RI · On-site
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 ...
Manager, Quality Assurance TCR
Cranston, RI · On-site
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 ...
Senior Salesforce QA Analyst
Providence, RI · On-site
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
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 ...
QA Engineering Technician IV
Newport, RI · On-site
$32.25/hr
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 ...
QA Engineering Technician IV
Newport, RI · On-site
$32.25/hr
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 ...
Qa 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 qa associate jobs pay per hour?
As of Sep 1, 2026, the average hourly pay for qa 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 is a QA associate?
QA Associates, or Quality Assurance Associates, are professionals responsible for monitoring, inspecting, and proposing measures to improve processes that ensure the quality of products or services in a company. They work closely with production, development, and compliance teams to make sure that products meet required standards and regulations. Their tasks often include reviewing documentation, conducting audits, and reporting on quality metrics. QA Associates play a crucial role in maintaining customer satisfaction and regulatory compliance in industries such as pharmaceuticals, manufacturing, and software.
What are the key skills and qualifications needed to thrive as a QA associate?
To thrive as a QA Associate, you need a solid understanding of quality assurance methodologies, attention to detail, and often a degree in a scientific or technical field. Familiarity with tools like LIMS, GMP/GLP regulations, and quality management systems, as well as relevant certifications such as ASQ or Six Sigma, is typically required. Strong analytical thinking, effective communication, and problem-solving abilities help you excel within cross-functional teams. These skills ensure product compliance, support continuous improvement, and maintain high standards in regulated environments.
What are some common challenges faced by a QA associate, and how can they be addressed?
QA Associates often encounter challenges such as managing tight deadlines, adapting to rapidly changing project requirements, and ensuring thorough test coverage. Effective communication with developers and other team members is crucial to address issues quickly and maintain product quality. Staying organized, using test management tools, and participating in regular stand-up meetings can help QA Associates stay on top of their workload and deliver consistent results.
Is a QA associate a difficult job?
A QA associate role involves testing products or software to identify defects, which requires attention to detail, analytical skills, and knowledge of testing tools. The job can be challenging depending on project complexity and deadlines but is generally manageable with proper training and experience.
Is a QA associate a good entry level job?
A QA associate position is often suitable for entry-level candidates, as it typically requires basic knowledge of testing processes, attention to detail, and familiarity with tools like test management software. It provides a foundation in quality assurance practices and can lead to more advanced roles in software testing or quality management.
What does a QA associate do?
A QA associate is responsible for testing products, software, or processes to ensure they meet quality standards and specifications. They develop test plans, identify defects, document issues, and work with teams to improve quality, often using testing tools and following industry protocols.
What are the most commonly searched types of Qa jobs in Rhode Island?
The most popular types of Qa jobs in Rhode Island are:
What cities in Rhode Island are hiring for Qa Associate jobs?
Cities in Rhode Island with the most Qa Associate job openings:
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