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 ...
Pharmaceuticals Title: QA Associate, Quality Operations Job ID: NORT000038 Location: Norton, MA (Onsite) Duration: 06 months contract (+Possibility of extension) *High possibility of role converting ...
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Pharmaceuticals Title: QA Associate, Quality Operations Job ID: NORT000038 Location: Norton, MA (Onsite) Duration: 06 months contract (+Possibility of extension) *High possibility of role converting ...
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 ...
Summary/Objective The Showroom Quality Assurance Associate "handy-man" ensures that the kitchen and bath showrooms are maintained at high standards, supports the installation of displays, and ...
Summary/Objective The Showroom Quality Assurance Associate "handy-man" ensures that the kitchen and bath showrooms are maintained at high standards, supports the installation of displays, and ...
Analytical Quality Assurance, Associate Director
$156K - $234K/yr
The Associate Director (AD) Quality Assurance (QA for QC) is an advanced technical resource in the principles and application of quality assurance and compliance. This role is responsible for the ...
Analytical Quality Assurance, Associate Director
$156K - $234K/yr
The Associate Director (AD) Quality Assurance (QA for QC) is an advanced technical resource in the principles and application of quality assurance and compliance. This role is responsible for the ...
Analytical Quality Assurance, Associate Director
Boston, MA · On-site
$156K - $234K/yr
The Associate Director (AD) Quality Assurance (QA for QC) is an advanced technical resource in the principles and application of quality assurance and compliance. This role is responsible for the ...
Analytical Quality Assurance, Associate Director
Boston, MA · On-site
$156K - $234K/yr
The Associate Director (AD) Quality Assurance (QA for QC) is an advanced technical resource in the principles and application of quality assurance and compliance. This role is responsible for the ...
Associate Director, Quality Assurance - CMC
$180K - $195K/yr
Reporting to the Head of Quality, Seaport Therapeutics is seeking an experienced Associate Director, Quality Assurance CMC to manage GMP quality assurance activities supporting clinical development ...
Associate Director, Quality Assurance - CMC
$180K - $195K/yr
Reporting to the Head of Quality, Seaport Therapeutics is seeking an experienced Associate Director, Quality Assurance CMC to manage GMP quality assurance activities supporting clinical development ...
Associate Director, Quality Assurance - CMC
Boston, MA · On-site
$180K - $195K/yr
Reporting to the Head of Quality, Seaport Therapeutics is seeking an experienced Associate Director, Quality Assurance CMC to manage GMP quality assurance activities supporting clinical development ...
Associate Director, Quality Assurance - CMC
Boston, MA · On-site
$180K - $195K/yr
Reporting to the Head of Quality, Seaport Therapeutics is seeking an experienced Associate Director, Quality Assurance CMC to manage GMP quality assurance activities supporting clinical development ...
Quality Assurance Supervisor
Franklin, MA · On-site
Education Requirements Bachelor's degree is desirable, associate degree with equivalent experience ... Certificate in quality assurance is a plus. Physical Requirements: * Frequent performing repetitive ...
New
Quality Assurance Supervisor
Franklin, MA · On-site
Education Requirements Bachelor's degree is desirable, associate degree with equivalent experience ... Certificate in quality assurance is a plus. Physical Requirements: * Frequent performing repetitive ...
New
Working in support of the Associate Director of Quality Assurance, the Quality Assurance Specialist will ensure that Care Access maintains a high level of quality while executing clinical trials ...
Working in support of the Associate Director of Quality Assurance, the Quality Assurance Specialist will ensure that Care Access maintains a high level of quality while executing clinical trials ...
The Associate Director, Quality Assurance ManufacturingTechnical Services(Internal)is responsible forsupporting the day-to-day Quality Operations for internal manufacturing of Cell & Gene Programs ...
The Associate Director, Quality Assurance ManufacturingTechnical Services(Internal)is responsible forsupporting the day-to-day Quality Operations for internal manufacturing of Cell & Gene Programs ...
Description The Quality Assurance Professional will work in the Internal QA team of Client's Human Genetic Therapies Quality Assurance Department. This unit oversees internal manufacturing on behalf ...
Description The Quality Assurance Professional will work in the Internal QA team of Client's Human Genetic Therapies Quality Assurance Department. This unit oversees internal manufacturing on behalf ...
Company Description Jobsbridge Dear Associate, We have this following position open. Please respond if interested. Title : Clinical QA Lead Location : Boston, MA Duration : 6+ Months 1. Minimum of 5 ...
Company Description Jobsbridge Dear Associate, We have this following position open. Please respond if interested. Title : Clinical QA Lead Location : Boston, MA Duration : 6+ Months 1. Minimum of 5 ...
Provide QA training support for QA operators Qualifications * College level education desired ... At Primo Brands, our more than 11,000 associates are at the heart of what we do and deliver on our ...
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Provide QA training support for QA operators Qualifications * College level education desired ... At Primo Brands, our more than 11,000 associates are at the heart of what we do and deliver on our ...
Quality Assurance Technician
Taunton, MA · On-site
$32.51/hr
Provide QA training support for QA operators Qualifications * College level education desired ... At Primo Brands, our more than 11,000 associates are at the heart of what we do and deliver on our ...
Quality Assurance Technician
Taunton, MA · On-site
$32.51/hr
Provide QA training support for QA operators Qualifications * College level education desired ... At Primo Brands, our more than 11,000 associates are at the heart of what we do and deliver on our ...
Quality Assurance Coordinator
Boston, MA · On-site
$60K - $68K/yr
REPORTS TOManager of Quality Planning and AssuranceABOUT THE POSITIONUnder the supervision and direction of the Manager of Quality Planning and Assurance, the Quality Assurance Coordinator will ...
Quality Assurance Coordinator
Boston, MA · On-site
$60K - $68K/yr
REPORTS TOManager of Quality Planning and AssuranceABOUT THE POSITIONUnder the supervision and direction of the Manager of Quality Planning and Assurance, the Quality Assurance Coordinator will ...
Quality Assurance Analyst
Boston, MA · On-site
Lynn (Greater Boston Area), MA We are looking for a Quality Assurance Analyst to collaborate on one of our projects in the aerospace sector. Who are we? Scalian is a multinational engineering ...
Quality Assurance Analyst
Boston, MA · On-site
Lynn (Greater Boston Area), MA We are looking for a Quality Assurance Analyst to collaborate on one of our projects in the aerospace sector. Who are we? Scalian is a multinational engineering ...
Quality Assurance Analyst
Boston, MA · On-site
Lynn (Greater Boston Area), MA We are looking for a Quality Assurance Analyst to collaborate on one of our projects in the aerospace sector. Who are we? Scalian is a multinational engineering ...
Quality Assurance Analyst
Boston, MA · On-site
Lynn (Greater Boston Area), MA We are looking for a Quality Assurance Analyst to collaborate on one of our projects in the aerospace sector. Who are we? Scalian is a multinational engineering ...
Quality Assurance Specialist
Mansfield, MA · On-site
$60K - $68K/yr
Associate degree * Prior work experience within a quality assurance program/department * Demonstrated technical writing skills * Technical background gained through education or relevant ...
Quality Assurance Specialist
Mansfield, MA · On-site
$60K - $68K/yr
Associate degree * Prior work experience within a quality assurance program/department * Demonstrated technical writing skills * Technical background gained through education or relevant ...
Quality Assurance Associate information
See Woonsocket, RI salary details
$12.44 - $16.71
17% of jobs
$18.12 is the 25th percentile. Wages below this are outliers.
$16.71 - $20.98
24% of jobs
The median wage is $23.12 / hr.
$20.98 - $25.25
18% of jobs
$25.25 - $29.53
15% of jobs
$29.88 is the 75th percentile. Wages above this are outliers.
$29.53 - $33.80
10% of jobs
$33.80 - $38.07
8% of jobs
$38.07 - $42.34
5% of jobs
$42.34 - $46.61
3% of jobs
$46.61 - $50.88
0% of jobs
$50.88 - $55.16
0% of jobs
$55.16 - $59.43
0% of jobs
$12
$28
$59
How much do quality assurance associate jobs pay per hour?
As of Aug 30, 2026, the average hourly pay for quality assurance associate in Woonsocket, RI is $28.07, according to ZipRecruiter salary data. Most workers in this role earn between $17.98 and $32.93 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 Woonsocket, RI?
The most popular types of Quality Assurance jobs in Woonsocket, RI are:
What cities near Woonsocket, RI are hiring for Quality Assurance Associate jobs?
Cities near Woonsocket, RI 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