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Quality Systems Associate Jobs in Rhode Island (NOW HIRING)

CEDENT

Quality Assurance Associate I

Cumberland, RI · On-site

The QA Associate II/III independently conducts quality assurance audits of production records ... gaps within existing Quality Systems and propose solutions for functional management; 2. ...

Bodycote plc

Quality Manager

Cranston, RI · On-site

... action program and qualify associates through testing and training. * Maintain supplier ... Must be capable of making written recommendations for improving Quality Assurance Systems and ...

Prysmian

Quality Technician

Lincoln, RI · On-site

$28 - $30.25/hr

... System while working with advanced wire, cable, and compound manufacturing operations. We're ... Train production associates on: * Inspection equipment. * Testing procedures. * Data entry and ...

Amgen SA

Sr Specialist QA - Compliance

West Greenwich, RI · On-site

$89K - $123K/yr

Monitor readiness of quality systems and operational processes that are commonly scrutinized during ... Associate's degree and 10 years of regulatory compliance experience * Bachelor's degree and 6 years ...

Amgen, Inc.

Sr Specialist QA - Compliance

West Greenwich, RI · On-site

$89K - $123K/yr

Monitor readiness of quality systems and operational processes that are commonly scrutinized during ... Associate's degree and 10 years of regulatory compliance experience OR * Bachelor's degree and 6 ...

Amgen

Sr Specialist QA - Compliance

West Greenwich, RI · On-site

$89K - $123K/yr

Monitor readiness of quality systems and operational processes that are commonly scrutinized during ... Associate's degree and 10 years of regulatory compliance experience OR * Bachelor's degree and 6 ...

Vatn Systems

Quality Technician

Bristol, RI

$18.75 - $25.25/hr

... associate degree or technical certificate a plus Preferred Skills * Experience in start-up ... Experience helping stand up an incoming inspection program Vatn Systems is an equal opportunity ...

Vatn Systems

Quality Technician

Bristol, RI · On-site

$18.75 - $25.25/hr

... associate degree or technical certificate a plus Preferred Skills * Experience in start-up ... Experience helping stand up an incoming inspection program Vatn Systems is an equal opportunity ...

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Quality Systems Associate information

What is the difference between Quality Systems Associate vs Quality Control Technician?

AspectQuality Systems AssociateQuality Control Technician
CertificationsISO auditor, GMP, or quality management certificationsGMP, HACCP, or industry-specific testing certifications
Work EnvironmentDocument control, quality management systems, auditsProduct testing, inspection, sampling
Employer & Industry UsageManufacturing, pharmaceuticals, biotechFood, pharmaceuticals, manufacturing

The Quality Systems Associate focuses on maintaining and improving quality management systems, documentation, and compliance. In contrast, the Quality Control Technician primarily conducts product testing and inspections to ensure quality standards are met. Both roles are essential in quality assurance but differ in their core responsibilities and daily tasks.

Is a Quality Systems Associate an entry level job?

A Quality Systems Associate position is often considered entry level, suitable for candidates with a bachelor's degree in a related field and some familiarity with quality management systems like ISO or GMP. The role typically involves supporting quality processes, documentation, and audits, and may require basic knowledge of tools such as SAP or TrackWise. Experience requirements vary by employer, but many entry-level candidates can qualify with relevant internships or certifications.

What is a quality systems associate?

A quality systems associate is responsible for maintaining and improving a company's quality management system, ensuring compliance with industry standards such as ISO 9001. They often perform audits, document control, and data analysis, and may use tools like quality management software to support continuous improvement efforts.

What are the most commonly searched types of Quality Systems jobs in Rhode Island?

The most popular types of Quality Systems jobs in Rhode Island are:

Infographic showing various Quality Systems Associate job openings in Rhode Island 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 87% Physical, 2% Hybrid, and 11% Remote job distribution.

Quality Assurance Associate I

Cumberland, RI • On-site

CEDENT
IT Services • 11 - 50 employees
Learn more about CEDENTexternal

Full-time

Re-posted 20 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

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

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