Quality assurance specialist jobs in Warwick, RI - 420 jobs
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Quality Assurance Specialist
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Quality Lead
Quality Assurance Auditor
Quality Assurance Specialist 21CFR GMP
Top Prospect Group
Quality assurance specialist job in Fall River, MA
Please note our client does not Sponsor
Job Role: IT-QA
Work Hours: General: 8:00AM - 5:00PM (May vary based on business needs)
Reports To: Site Quality Assurance Head
Salary Range: $67,000 - $95,000 -
PURPOSE
The purpose of the IT - QA Associate position is to accurately review the chronological record of Laboratory Instrument/Equipment electronic data related activities that provides documented evidence of relevant details of specific events.
JOB DESCRIPTION
The IT- QA Associate position is an individual contributor role and a member of the Pharmaceuticals Quality Team. The position monitors changes to electronic records, alterations in critical parameters or any other actions that could impact product quality. This position reports to the Site Quality Head.
The job duties for this position include but are not limited to the following:
Function as SME for IT related activities of QMS platforms and other electronic systems including digital platforms which need compliance to 21CFR, Part 11 requirements.
Conduct regular audits of the audit trail to identify any irregularities or potential issues. Additionally, routinely review and analyze the data to proactively address any emerging trends or areas for improvement.
Provide comprehensive training to employees involved in the analytical laboratory related activities as well as manufacturing process who are entitled to use digital platforms for execution of GMP/GLP activities. Ensure that users understand the importance of audit trail integrity and data integrity and their role in maintaining accurate and reliable records and adhering to cGMP compliance.
Provide support for investigation and implementation of CAPA related to such investigation.
EDUCATION AND EXPERIENCE QUALIFICATIONS
B.Sc. in a scientific discipline related to the pharmaceutical industry (Biology, Chemistry, Pharmacology, Biochemistry, etc).
Basic knowledge and Industry experience of Quality System relevant to electronic records storage, retrieval, archival and audit of electronic data is must.
Minimum of two (2) years' experience in a quality assurance in a GMP environment specific Quality Control Laboratory and Manufacturing operations in a pharmaceutical manufacturing organization.
Experience in MDI or DPI dosage form manufacturing preferred.
KNOWLEDGE, SKILLS, AND ABILITIES
Candidates must have an aptitude for quantitative problem-solving or advanced analytics.
Ability to multitask efficiently, prioritize quickly, and manage time effectively.
Candidates must have experience in writing and executing performance tests.
Database and computer skills; talent for analyzing and visualizing complex data.
Advanced proficiency with Microsoft Excel.
Must have current Good Manufacturing Practices (cGMP) knowledge.
Must have strong attention-to-detail.
Must be a self-starter and demonstrate initiative with seeking additional training or direction as needed.
Must have strong organization and communication skills (written, verbal, and presentation).
Must be detail-oriented with the ability to prioritize tasks with strict deadlines.
$67k-95k yearly 2d ago
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Quality Assurance Manager
Tedor Pharma Services 3.9
Quality assurance specialist job in Cumberland, RI
The ideal candidate is a critical thinker who will proactively improve the quality systems of the company through internal audits, participation in process improvement programs, and interaction with key partners to obtain constructive feedback.
Responsibilities
Develop standardized production, quality, and customer-service standards
Identify potential risks before they become a problem, focusing on root cause analysis and preventive action
Perform internal and external quality audits and compile detailed reports of findings
Build a strong team through coaching, mentoring, specific training and performance evaluations
Qualifications
Bachelor's degree or equivalent experience in Engineering
5+ years' relevant work experience
Highly organized with excellent attention to detail
$78k-112k yearly est. 17h ago
Quality Systems & Investigations Specialist
JMD Technologies Inc.
Quality assurance specialist job in Boston, MA
Title: Quality Systems & Investigations Specialist
Employment Type: Contract
Status: Accepting Candidates
About the role
This position plays a key role in supporting daily manufacturing activities by resolving operational issues and driving high-quality investigations. The role ensures process reliability through strong technical oversight and collaboration with critical operations teams.
Key Responsibilities
• Lead real-time floor support, triaging deviations and initiating root cause investigations.
• Produce thorough, compliant quality documentation for deviations, CAPAs, and impact assessments.
• Partner with manufacturing, QC, facilities, and materials teams to define corrective and preventive actions.
• Apply structured scientific thinking to evaluate data and support operational decisions.
• Contribute to process improvement by identifying trends and proposing optimized workflows.
Qualifications
• 6+ years experience in pharma/biotech manufacturing environments.
• Proven background in investigations, RCA, QC analytics, and GxP documentation.
• Skilled in cross-functional coordination and rapid issue assessment.
• Strong analytical mindset with the ability to interpret complex data sets.
• Experience supporting manufacturing operations in fast-paced, regulated environments.
Compensation (MA Pay Transparency):
• Estimated hourly range: $50-$58/hr (W-2).
• Final rate within this range will be based on skills, experience, and interview results.
$50-58 hourly 4d ago
US/LATAM Spanish LQL Linguistic Quality Lead
Csoft International
Quality assurance specialist job in Boston, MA
Schedule: Mon-Fri (4 days in office required, 1 day optional remote)
Compensation: Competitive Salary + Benefits
We are a fast-growing AI language technology company seeking a US/LATAM Spanish Linguistic Quality Lead (LQL) to join our AI-focused language team on a mission to build the next generation of operational models. This is a unique opportunity for someone passionate about languages and technology, with the drive to shape the future of AI-powered communication in medical and life sciences translation.
What You'll Do
Lead linguistic quality assurance for US/LATAM Spanish, with a strong focus on medical device manuals, pharmaceutical content, and other regulated life sciences materials.
Train large language models (LLMs) with Spanish linguistic data to enhance AI-driven translation, QA, and automation workflows.
Translate, review, and edit Spanish content in active projects, ensuring accuracy, clarity, and regulatory compliance.
Recruit, onboard, and manage Spanish linguistic resources (translators, editors, interpreters, interviewers) within our global network.
Support project execution, ensuring linguistic excellence and cultural relevance across deliverables.
Collaborate with other LQLs to drive workflow improvements and innovation, helping design future operational models.
Partner with cross-functional teams at the intersection of language, life sciences, and AI.
What We're Looking For
Native proficiency in US/LATAM Spanish, with strong command of English.
Ideal for your graduates with Spanish linguistic background.
Familiarity with CAT tools (e.g., Phrase, Trados, MemoQ, XTM) is a plus but not required.
Forward-thinking, creative, and energetic, with a willingness to take on challenges and think outside the box.
Diligent, dependable, and committed to quality and continuous improvement.
Strong organizational, communication, and problem-solving skills.
Ability to work collaboratively with other LQLs, engineers, and project teams in a fast-paced, innovative environment.
Work authorization in the U.S. is required.
What We Offer
Full-time role: Monday-Friday, with 4 days in-office and 1 day optional remote.
Competitive salary + paid holidays, sick/personal days, and professional development opportunities.
A modern office in Boston's Financial District.
The chance to contribute to an AI-driven language team pioneering future business and operational models.
A dynamic, entrepreneurial environment where your ideas and contributions have direct impact.
This is an exciting role for someone passionate about Spanish language and culture, eager to explore AI-powered translation and linguistic innovation, and motivated to grow with a company shaping the future of language operations in medical and life sciences.
How to Apply: Please send your CV to **********************
$88k-131k yearly est. 1d ago
Quality Systems Specialist
Advantage Technical
Quality assurance specialist job in Waltham, MA
Pay Rate: $40-$50/hr Work Model: Hybrid (Onsite Tuesday, Wednesday, Thursday)
The Quality Systems Specialist, under the direction of the QS&C management team, supports global Quality Systems to ensure compliance, operational effectiveness, and fitness for intended use in alignment with applicable global SOPs.
Key Areas of Accountability
Quality System Governance & Support
Assist in governance of Quality System applications, including harmonizing processes across sites
Participate in meetings/workshops with Site Process Owners and business SMEs to gather requirements for system improvements and ongoing maintenance
Join user forums to collect ongoing requirements, prioritize needs, and triage issues
Follow up on requests, issues, and project activities; provide status updates to managers and working teams
Change Control & Compliance
Initiate and manage change controls through completion, including all required documentation
Ensure systems remain in a validated state by supporting periodic user access reviews, change management, business administration, and deviations/CAPAs
Support investigation, escalation, and resolution of system-related issues
Validation & Documentation
Support validation activities, including:
Requirements gathering
Validation planning
Design qualification
Authoring and executing test plans and test scripts
Discrepancy management
Preparing system descriptions and validation summary reports
Maintain user-related documentation and ensure updates as new functionalities are introduced
Cross-Functional & User Support
Assist manager with communication between vendor/IT teams
Provide customer support through system administration, training management, and onboarding of new users
Generate metrics to support Quality Systems performance
Support regular system updates/releases and provide assessments and recommendations on new features
Academic & Technical Qualifications
Bachelor's degree or higher in a relevant computer, technical, quality, or scientific discipline (multi‑disciplinary background preferred)
3-6 years of experience in a high‑volume commercial or clinical pharma/healthcare environment
Proficiency in MS Word, Excel, and Quality System processes
Experience with Veeva Vault Quality Docs, TrackWise, and ComplianceWire is a plus
Strong understanding of US FDA and European regulatory requirements, GAMP, and phase‑appropriate compliance expectations
Knowledge of Regulatory Compliance and ICH Guidelines
General Comments
Position Title: Quality Systems Specialist
Pay Rate Range: $40-$50/hr
$40-50 hourly 1d ago
Associate, Quality Operations QA
Talentburst, An Inc. 5000 Company 4.0
Quality assurance specialist job in Norton, MA
Industry: Pharmaceuticals
Title: Associate, Quality Operations QA
Duration: 09 months contract (+Possibility of extension)
Onsite with 1x per week flexibility as needed.
About the Role
The QA Associate will help ensure that life-changing biopharmaceutical products are manufactured to the highest standards. The QA Associate will provide day-to-day QA support across manufacturing, validation, materials, QC, engineering and facility operations at our Norton site, partnering with cross-functional teams to maintain GMP compliance and inspection readiness.
Key Responsibilities
Provide raw material support, including review/approval of incoming material documentation and release for GMP use.
Deliver on-the-floor QA support to manufacturing, including area clearance and changeover operations, ensuring readiness for production activities.
Review and approve SOPs, master batch records (MBRs), specifications, risk assessments, and quality documents.
Generate and maintain Quality-related SOPs and controlled forms.
Review and approve validation documents and protocol executions to confirm compliance with approved procedures and regulatory requirements.
Review and approve QC laboratory qualification documents, including equipment qualification.
Perform executed batch record review and approval to ensure accuracy and compliance.
Review and approve deviations, CAPAs, Change Controls and related investigations in the quality management system.
Support partner audits and regulatory inspections, including document retrieval and subject matter input.
Approve work orders in the maintenance system to verify equipment maintenance and calibration compliance.
Collaborate with internal cross-functional teams at the Norton facility to drive continuous improvement and quality excellence.
Qualification/Skills
Bachelor's degree in a scientific or engineering discipline (Biology, Chemistry, Biotechnology, etc.) or equivalent experience.
2-4 years of GMP experience in Quality, Manufacturing, or QC.
Knowledge of cGMP regulations (21 CFR Parts 210/211/11, ICH Q7/Q10) and Good Documentation Practices.
Strong attention to detail, organizational skills, and the ability to communicate effectively across teams.
Experience with quality systems (e.g., Veeva, SAP) is a plus.
$57k-71k yearly est. 3d ago
Quality Assurance Manager - Food Safety
LSG Sky Chefs 4.0
Quality assurance specialist job in Boston, MA
Job Title: Quality Assurance Manager - Food Safety Salary Range: $90 000.00
About us
LSG Sky Chefs is one of the world's largest airline catering and hospitality providers, known for its outstanding reputation and dynamic approach in the industry. Voted "Airline Caterer of the Year in North America" for 2023 and 2024, we are committed to excellence and innovation, driven by the dedication and expertise of our talented employees. Our team members are the heart and soul of our success, consistently delivering exceptional culinary experiences and outstanding service to our clients and their passengers across North and Latin America.
Role Purpose Statement
Ensure the food meets the standards set by regulatory health authorities and the company. The job incumbent is responsible for the implementation, auditing, assessing and training of food safety and quality management systems within the responsible Customer Service Center (CSC).
Responsible for the development, deployment, implementation, and on-going execution of the food safety preventive controls program (Policies, SOPs, Hazard Analysis, HACCP Plan, Prerequisite Food Safety Programs, Traceability & Recall Process, Allergen Programs, and Associated Records) within the assigned facility.
Main Accountabilities
Ensure compliance with regulatory requirements Food and Drug Administration (FDA) such as federal regulation, local regulation, United States Department of Agriculture (USDA), customer specifications and corporate food safety and quality standards, regional food safety and quality standards, taken appropriate corrective actions when needed.
Manage the food safety program and ensures that FDA FSMA preventive controls are effective and proper records are maintained.
Provide technical expertise relative to Hazard Analysis and Critical Control Points (HACCP), food safety, sensory and quality evaluations.
Conduct monthly-required assessments of the food safety program to ensure compliance.
Conduct routine microbiological testing as defined by food safety program.
Review and analyse weekly food safety documents including HACCP logs.
Utilization of the checklists to determine consistent fulfilment of required food safety program.
Support CSC leadership with inspection/audit readiness; coach CSC before, during and after all external, food safety, quality and sanitation inspections/audit.
Supervise pest control program and contract services and suppliers related to the food safety program.
Conduct appropriate investigations regarding food safety matters and support CSC management in providing detailed information to the customers.
Perform and document periodical checks on products and services to ensure quality standards are met.
Interface with functional areas (Operations, Production, Sales, and HR), Regional Quality Team, other quality managers to ensure sustainability of the food safety program.
Establish and maintain effective working relationships with internal stakeholders across all functions and suppliers, customers and regulatory authorities.
Reporting
Monitor and prepare reports for the food safety and quality management system.
Insertion of monthly-required data in the company web based portal.
Collect and monitor all food safety and quality documents (e.g. environmental monitoring, sanitation verifications, chef table, portion control, equipment handling, ramp-on time and safety performance)
Keep manuals and documentation updated and implement new procedures and rules in a timely manner.
Leadership
Possess excellent verbal and written communication skills, including the ability to communicate professionally in person, by phone and through email.
Must be able to work in a fast-paced environment while interacting with staff at all levels, and remaining positive, proactive and resourceful.
Demonstrates initiative and the ability to work efficiently and independently.
Able to read and understand food safety and quality reports and take appropriate action.
Must possess a high level of accuracy, attention to detail and is well organized.
Recruit, on-board, develop, coach, train, support, and evaluate the performance of the Food Safety staff.
Participate and support company sponsored initiatives such as Global Quality Standards (GQS), HACCP, Lean Manufacturing, Employee Safety
Knowledge, Skills and Experience
Bachelor's degree in Food Science, Food Microbiology, Chemistry, Biology or related fields.
Certified Preventive Controls Qualified Individual (PCQI) and Hazard Analysis Critical Control Points (HACCP)
Five or more years of experience in Food Safety roles with a minimum of 2 years management experience.
Technical proficiency in the areas such as of food microbiology, food chemistry, food safety, and food regulations.
Proven understanding of government regulations in relation to food processing as FDA FSMA, Current Good Manufacturing Practices (cGMP), HACCP regulations and USDA.
Proven analytical and leadership skills.
Strong interpersonal and communication skills.
Be a collaborative leader who inspires, manages, coaches and respects people.
Excellent verbal, written and organizational skills that combines with an aptitude for multi-tasking.
Knowledge of computer skills required, including use of technology (scanners, tablets, printers, copiers, etc.) and Microsoft Office programs, as well as cloud based systems
LSG Sky Chefs is an EEO and Affirmative Action Employer of Women/Minorities/Veterans/Individuals with Disabilities.
$90k yearly 17h ago
QUALITY ASSURANCE MANAGER
City of Worcester 4.0
Quality assurance specialist job in Worcester, MA
DEPARTMENT OF EMERGENCY COMMUNICATIONS CITY OF WORCESTER
The City of Worcester is seeking qualified applicants for the position of Quality Assurance Manager within the Department of Emergency Communications. The Quality Assurance Manager will provide quality assurance (QA), quality improvement (QI), and public education support to the Regional Communications Center which oversees 911, 311 and Emergency Management. Under the supervision of the Deputy Director of Emergency Management, the QA Manager is responsible for the creation, development, deployment, and ongoing operation of a comprehensive quality assurance and quality improvement program to ensure that products and/or services are consistently meeting City standards and working correctly and efficiently. The work schedule will consist of Monday-Friday, with the ability to flex the work schedule based on the needs of the overall QA/QI program and Public Education efforts.
Bilingual applicants are encouraged to apply
ESSENTIAL ELEMENTS:
Maintain, evaluate, and update the formal QA/QI program and assist in the development and revision of policies governing 911 call-taking operations, and quality standards.
Establish objective performance metrics and scoring criteria aligned with agency policies and industry standards.
Identify trends, performance gaps, and training needs through data analysis and call review.
Prepare, review and edit various documents and analytical reports.
Monitor and evaluate incoming and outgoing telephone calls to ensure that delivery of services provided to citizens meets or exceeds expectations, that resources are being utilized appropriately, and to address complaints, failures, and mistakes expeditiously.
Monitor and evaluate two-way radio traffic transmissions to ensure conformity with policies, procedures, and practices
Create, develop, and distribute public education materials.
Create, develop, and oversee a public education and awareness team consisting of current telecommunicators who will attend events and functions, provide materials, present demonstrations, lead classes, and more.
Recommend and consult on training programs and classes, and other initiatives for the department as needed.
Maintain, evaluate, and update the formal QA/QI program and assist in the development and revision of policies governing 911 call-taking operations, and quality standards.
Establish objective performance metrics and scoring criteria aligned with agency policies and industry standards.
Identify trends, performance gaps, and training needs through data analysis and call review.
Work collaboratively with supervisors, managers, and line staff to foster a culture of accountability and continuous improvement.
Assist in disaster preparation for the Emergency Management Division when large scale emergencies occur.
Other duties as assigned.
REQUIRED KNOWLEDGE, SKILLS, AND ABILITIES:
Demonstrated computer proficiency; proficiency with Microsoft Office Suite (Word, Excel, Outlook, PowerPoint)
Knowledge of quality assurance best practices
Familiarity with two-way radio
Excellent verbal and written communications skills
Strong organizational skills and flexibility
Detail oriented with a high degree of accuracy
Ability to self-direct
Ability to maintain confidentiality
Ability to complete projects with limited supervision
Ability to work independently and as part of a team
Regular onsite attendance is required
Ability to coordinate and facilitate projects and meetings with partners to effectively accomplish department goals
Ability to establish and maintain professional relationships with diverse and vulnerable populations, and organizations
Ability to drive sport utility or pick-up type vehicles with trailers
Ability to work in an outside environment
MINIMUM REQUIREMENTS:
Bachelor's Degree in Criminal Justice, Business Management, Public Administration, or a related field;
Three (3) years of experience as a public safety telecommunicator;
OR,
An equivalent combination of education, training and five (5) years of related experience which provide the required knowledge, skills and abilities to perform the required duties of the position will be considered in lieu of the above-mentioned requirements.
Certification to perform as a 9-1-1 telecommunicator as prescribed by the MA State 911 Department.
Must complete formal Quality Assurance and Improvement Training Program within twelve (12) months of hire.
Successful results of CORI and FBI fingerprint check.
Valid driver's license and access to reliable transportation.
Excellent communication skills.
PREFERRED QUALIFICATIONS:
Master's Degree in Criminal Justice, Business Management, Public Administration, or a related field.
Five (5) years of progressive experience as a public safety telecommunicator.
SALARY RANGE: $78,080 - $102,040 annually, full-time, exempt, with an excellent benefits package.
To apply, please visit: ****************************** or send resume and cover letter to: City of Worcester, 455 Main Street, Room 109, Worcester, MA 01608. OPEN UNTIL FILLED, applications received prior to or on FRIDAY, JANUARY 16, 2026, will receive preference. Preference is given to Worcester residents. The City of Worcester is an equal opportunity, affirmative action employer. Women, minorities, people with disabilities and protected veterans are encouraged to apply. Direct inquiries to: City Hall, Human Resources, Room 109, ************, .
$78.1k-102k yearly 1d ago
Quality Assurance Auditor
Thales 4.5
Quality assurance specialist job in North Kingstown, RI
Location: North Kingstown, United States of AmericaThales people architect identity management and data protection solutions at the heart of digital security. Business and governments rely on us to bring trust to the billons of digital interactions they have with people. Our technologies and services help banks exchange funds, people cross borders, energy become smarter and much more. More than 30,000 organizations already rely on us to verify the identities of people and things, grant access to digital services, analyze vast quantities of information and encrypt data to make the connected world more secure.
Position Summary
This is an on-site position in North Kingstown, RI.
This position is eligible for the Americas referral program for external candidates: Tier 1 - $2500 Referral Bonus.
Provide quality service to our customer's by the internal auditing of their mail kit product to ensure that the highest production and quality is achieved according to established standards and procedures.
Key Areas of Responsibility
General understanding of client's completed mail kit product: Job sheet reading/ filling, ISO/ CQM requirements, Process understanding, Control plan interpretation. Understanding of calibration and verification concepts. Understanding of AQL, military standard concept and use. Understanding and application of Non conformity process. Fully understands and follows established QA procedures while performing the internal QA audit function.
Must be proficient in QA procedures.
Audits jobs from Data Card, Hand Fulfillment and Auto Inserting departments.
Understanding of Company's JAAMS system for department's audit input procedures. Hands-on knowledge and usage of job tracking system.
Generate non-conformance report to management.
Provide feedback to QA manager of any excessive errors discovered during the auditing process.
Provide support to production floor on inspection/ segregation of non-conforming product.
Validate new products/ portfolios.
Maintain a positive attitude and understanding toward fellow co-workers
Must be flexible with working nights and weekends as this may be required for major projects. Ensure conformance to vision, mission and values of the company.
Must be detail oriented and highly focused to meet the customer's expectations.
Ability to work independently with minimal supervision.
Minimum Requirements:
Education and/or Experience:
Must have 1 - 3 years' experience working in a manufacturing and/or production environment.
Bachelor's degree
preferred
.
Personal Characteristics: Basic analytical, numerical, and reasoning abilities. Well-developed interpersonal skills. Ability to get along with diverse personalities. Tactful and mature. Ability to work independently and self-directed.
Language Skills: Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Excellent people skills, attention to detail. Excellent communication skills, written and verbal skills required.
Mathematical Skills: Basic math skills required. Intermediate computer skills also needed.
Reasoning Ability: Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Results oriented with the ability to balance other business considerations.
#LI-Onsite
#LI-AS007
This position will require successfully completing a post-offer background check. Qualified candidates with [a] criminal history will be considered and are not automatically disqualified, consistent with federal law, state law, and local ordinances.
Successful applicant must comply with federal contractor vaccine mandate requirements.
Thales champions inclusion and we believe diversity strengthens the fabric of our culture. We are an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.
If you need an accommodation or assistance in order to apply for a position with Thales, please contact us at ************************************.
$84k-112k yearly est. Auto-Apply 60d+ ago
Documentation Specialist
Collabera 4.5
Quality assurance specialist job in Worcester, MA
Established in 1991, Collabera is one of the fastest growing end-to-end information technology services and solutions companies globally. As a half a billion dollar IT company, Collabera's client-centric business model, commitment to service excellence and Global Delivery Model enables its global 2000 and leading mid-market clients to deliver successfully in an increasingly competitive marketplace.
With over 8200 IT professionals globally, Collabera provides value-added onsite, offsite and offshore technology services and solutions to premier corporations. Over the past few years, Collabera has been awarded numerous accolades and Industry recognitions including.
• Collabera awarded Best Staffing Company to work for in 2012 by SIA. (hyperlink here)
• Collabera listed in GS 100 - recognized for excellence and maturity
• Collabera named among the Top 500 Diversity Owned Businesses
• Collabera listed in GS 100 & ranked among top 10 service providers
• Collabera was ranked:
• 32 in the Top 100 Large Businesses in the U.S
• 18 in Top 500 Diversity Owned Businesses in the U.S
• 3 in the Top 100 Diversity Owned Businesses in New Jersey
• 3 in the Top 100 Privately-held Businesses in New Jersey
• 66th on FinTech 100
• 35th among top private companies in New Jersey
***********************************************
Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance.
Job Description
The chosen candidate will be responsible for maintaining an accurate, cGMP compliant documentation change control system.
He/She will assign Change Request numbers for document and/or data changes.
Preparation of manufacturing records for issuance to production. Maintain tracking and distribution of controlled documentation.
Maintain master and historical document files and assist audits as required.
Candidate will also be required to route documents for approval.
Will assist in administrative tasks as needed.
Previous office experience would be good however would be willing to consider recent Graduates.
*** Position is listed for 12 months but could be extended based on need and performance ***
Qualifications
Prepares, edits, files, assembles documentation such as reports or technical documents, records, or correspondence. Maintains numerical, alphabetical, chronological and/or subject filing system. Responsible for file maintenance and record keeping; locates and removes file material upon request. 3-5 Years of experience.
Additional Information
All your information will be kept confidential according to EEO guidelines.
$80k-117k yearly est. 1d ago
Associate, Third Party Assurance
Banco Santander 4.4
Quality assurance specialist job in Boston, MA
Associate, Third Party AssuranceCountry: United States of America
It Starts Here:
Santander is a global leader and innovator in the financial services industry and is evolving from a high-impact brand into a technology-driven organization. Our people are at the heart of this journey and together, we are driving a customer-centric transformation that values bold thinking, innovation, and the courage to challenge what's possible. This is more than a strategic shift. It's a chance for driven professionals to grow, learn, and make a real difference.
If you are interested in exploring the possibilities We Want to Talk to You!
The Difference You Make:
As an Associate, Third Party Assurance, you will support FLOD Third Party Risk Management in working with business units to ensure third-parties are managed in accordance with the TPRM program. This function performs due diligence activities including, but not limited to data governance, cyber security, and operational risk.
As a member of the team, the Associate, Third Party Assurance implements various risk management processes and strategies for supporting initiatives, capturing and implementing recommendations from audits and other internal/compliance and external/regulatory assessment projects, and employing risk.
Applies innovative quantitative and qualitative analytical techniques to detect problems and improve reporting/MIS capabilities.
Delivers industry best practices, tools, guidance, and training to increase analytical capabilities and throughput.
Partners with Business Lines to recommend and vet new products initiatives, origination strategies, pre-approval and pre-qualification campaigns, underwriting techniques, peer group comparisons, and process optimization.
Implements and validates various risk segmentation strategies using complex data.
Provides direct support, participation, and oversight for developing, managing, and executing the credit risk strategy, which specifically includes functions such as understanding and leveraging credit-risk analytics to improve portfolio performance.
Selects and optimizes risk management processes and strategies for various Small Business initiatives, capturing and implementing recommendations from audits and other internal/compliance and external/regulatory assessment projects, and employing risk.
Provide monitoring and assessment of enterprise-wide adherence to vendor management policy requirements
Collaborate with colleagues and work towards streamlining processes
Consistently deliver on commitments, deadlines and objectives while remaining in scope and leveraging appropriate tools, methods, frameworks, and professional standards
Demonstrate the ability to appropriately influence business decisions, and the professional judgment for selecting the appropriate methods and techniques to do so
Conduct third party risk assessments, applying established criteria
Maintain thorough understanding of all business requirements to support requirements analysis
Analyze and develop requirements for enhancements to application functionality
Works will other Technical Security personnel to review and interpret vendor due diligence materials, including audit reports and security risk assessment questionnaires
Involve appropriate subject matter expertise as required to resolve vulnerabilities
Works with the Corporate Vulnerability Management team to conduct vulnerability assessments on remote hosted applications as needed
What You Bring:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Bachelor's Degree or equivalent work experience: Business, Finance, or equivalent degree. - Required.
5+ Years Risk Management - Required.
Advanced understanding of key inherent risk and risk management control practices.
Strong risk management principles, methodologies and tools, governance principles and activity preferably in a financial services technology environment.
Knowledge of workflow/processes and risks/controls, including: origination, underwriting, servicing, and collections/workout.
Ability to independently operate in a complex, matrixed environment; adept at delivering and maintaining productive working relationships across business, functions, geographies and lines of defense.
Ability to handle conflict resolution with other groups to ensure appropriate accounting guidance is followed.
Ability to adjust to new developments/changing circumstances.
Ability to convey a sense of urgency and drive issues/projects to closure.
Ability to effectively interact with the market, executive management and vendors.
Ability to adapt and adjust to multiple demands and competing priorities.
Excellent written and oral communication skills.
Strong analytical, organizational and project management skills.
Certifications:
No Certifications listed for this job.
It Would Be Nice For You To Have:
Established work history or equivalent demonstrated through a combination of work experience, training, military service, or education.
Experience in Microsoft Office products.
What Else You Need To Know:
The base pay range for this position is posted below and represents the annualized salary range. For hourly positions (non-exempt), the annual range is based on a 40-hour work week. The exact compensation may vary based on skills, experience, training, licensure and certifications and location.
Base Pay Range:
Minimum:
$80,625.00 USD
Maximum:
$140,000.00 USD
We Value Your Impact:
Your contribution matters and it's recognized. You can expect a fair and competitive rewards package that reflects the impact you create and the value you deliver. We know rewards go beyond numbers. Offering more than just a paycheck our benefits are designed to support you, your family and your well-being, now and into the future. Santander Benefits - 2026 Santander OnGoing/NH eGuide (foleon.com)
Risk Culture:
We embrace a strong risk culture and all of our professionals at all levels are expected to take a proactive and responsible approach toward risk management.
EEO Statement:
At Santander, we value and respect differences in our workforce. We actively encourage everyone to apply. Santander is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, genetics, disability, age, veteran status or any other characteristic protected by law.
Working Conditions:
Frequent minimal physical effort such as sitting, standing and walking is required for this role. Depending on location, occasional moving and lifting light equipment and/or furniture may be required.
Employer Rights:
This does not list all of the job duties of the job. You may be asked by your supervisors or managers to perform other duties. You may be evaluated in part based upon your performance of the tasks listed in this . The employer has the right to revise this at any time. This job description is not a contract for employment and either you or the employer may terminate your employment at any time for any reason.
What To Do Next:
If this sounds like a role you are interested in, then please apply.
We are committed to providing an inclusive and accessible application process for all candidates. If you require any assistance or accommodation due to a disability or any other reason, please contact us at ****************** to discuss your needs.
$80.6k-140k yearly Auto-Apply 5d ago
Home Health QA Coordinator
Acclaim Home Health
Quality assurance specialist job in Worcester, MA
Acclaim Home Health is seeking an experienced QA Coordinator to oversee and ensure the accuracy, compliance, and quality of clinical documentation in accordance with state, federal, and payer regulations. The QA Coordinator plays a critical role in supporting high-quality patient care by reviewing OASIS assessments, ensuring accurate coding, and promoting regulatory compliance and best practices across the organization.
Key Responsibilities
Review OASIS assessments for accuracy, completeness, and compliance with CMS guidelines
Ensure correct clinical coding (ICD-10) and documentation consistency
Identify trends, errors, and risk areas; provide feedback and education to clinical staff
Collaborate with clinicians, leadership, and billing to improve documentation quality and outcomes
Monitor compliance with Medicare Conditions of Participation and other regulatory requirements
Assist with audits (internal and external) and performance improvement initiatives
Stay current on OASIS updates, coding changes, and regulatory requirements
Qualifications
OASIS Certification required
Proven coding experience, including ICD-10 coding in a home health setting
Prior experience in home health quality assurance, clinical review, or utilization review preferred
Strong knowledge of Medicare regulations and home health compliance standards
Excellent attention to detail and analytical skills
Strong communication and collaboration skills
Ability to work independently and manage multiple priorities
Preferred Credentials
RN, LVN/LPN, or other licensed clinical background (preferred but not required, if applicable)
Previous experience with QA audits and performance improvement programs
Why Join Acclaim Home Health?
At Acclaim Home Health, we are committed to delivering exceptional patient-centered care while supporting our team members with a positive and professional work environment.
Acclaim Home Health is an Equal Opportunity Employer (EEO). We celebrate diversity and are committed to creating an inclusive environment for all employees.
$59k-86k yearly est. 3d ago
Documentation Specialist-I
Artech Information System 4.8
Quality assurance specialist job in Boston, MA
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Job Description
Tracking and reviewing change control documentation. Assist with the editing of quality documents (SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulatory requirements.
Must be able to work quickly with a high degree of accuracy.
Must possess sound interpersonal and information gathering skills, being able to relate well to others at all levels throughout the organization and have the ability to work in a team environment, effectively interacting with others.
Experience:
1 to 3 years Required
Skills:
Strong organizational skills
Attention to detail Ability to work cross-functionally Ability to organize work to meet deadlines
Qualifications
Education:
High School Diploma and 1-3 years administrative/professional experience
Experience with Microsoft Office products
Additional Information
For more information, Please contact
Sneha Shrivastava
************
$44k-74k yearly est. 1d ago
Quality Assurance Associate
Actalent
Quality assurance specialist job in Waltham, MA
We are seeking a dedicated Quality Assurance Associate to support on-the-floor QA issues within our manufacturing suite. You will play a crucial role in mitigating gaps and risks for all quality and GMP processes, and will run investigations for deviations, change controls, CAPAs, and out-of-specifications. Additionally, you will review and author SOPs to ensure compliance with industry standards.
Responsibilities
* Support on-the-floor QA issues within the manufacturing suite.
* Mitigate gaps and risks for all quality and GMP processes.
* Conduct investigations for deviations, change controls, CAPAs, and out-of-specifications.
* Review and author Standard Operating Procedures (SOPs).
Essential Skills
* Proficiency in quality assurance and document control.
* Experience with batch record review, CAPA, and deviation management.
* Knowledge of compliance, audits, and quality systems management.
* Familiarity with cGMP, FDA regulations (21 CFR Parts 211, 212), and ICH guidelines.
Additional Skills & Qualifications
* Bachelor's degree with 3-5 years of experience.
* Experience supervising or managing direct reports.
* Capability to support GMP requirements and compliance.
Work Environment
The role involves working with a team of 3-4 individuals. It is a first shift, Monday to Friday business casual environment, with occasional weekend work required. The company values hard-working individuals who are great team players. Enjoy contractor perks such as participation in all company events, a fully stocked kitchen, company-provided lunches twice a week, and access to an on-site gym that's open 24/7.
Job Type & Location
This is a Contract to Hire position based out of Waltham, MA.
Pay and Benefits
The pay range for this position is $43.00 - $45.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Waltham,MA.
Application Deadline
This position is anticipated to close on Jan 23, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Quality assurance specialist job in West Greenwich, RI
Employment Type: Contract Business Unit: Plant Quality Assurance Duration: 10 months with likely extensions or conversion to permanent
3 Key Consulting is hiring a Quality Assurance Senior Specialist for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Plant Quality Assurance (PQA) on-the-floor position will work directly with plant manufacturing and support groups for on-going bulk drug substance manufacturing.
Primary responsibilities of this position include:
Provide on-going Quality oversight to ensure products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and other applicable regulations
Drive closure/completion (including review and approve) of cGMP processes, procedures, documents and records, including but not limited to equipment used records, work orders, job plans, reports and batch records.
Ensure production and testing records/results are complete, accurate, and documented according to procedures, GDP and cGMP requirements.
Ensure facilities, equipment, materials, organization, processes and procedures comply with cGMP practices and other applicable regulations.
Complete required assigned training for self to permit execution of required tasks.
Perform training activities, as needed.
Support operational improvement initiatives, programs and projects.
Perform walkthroughs/inspections of areas to ensure housekeeping and GMP are maintained
Skills:
Quality assurance or manufacturing experience in the pharmaceutical or medical device industry
Strong cGMP and GDP behaviors
Strong word processing, presentation, database and spreadsheet application skills
Strong organizational skills and ability to manage multiple tasks at one time
Knowledge of electronic systems including LIMS, Trackwise, and Maximo.
Why is the Position Open?
Supplement additional workload on team.
Top Must-Have Skill Sets:
Ability to work in teams, flexible to work in an everchanging work environment
Quality assurance or manufacturing experience in the pharmaceutical or medical device industry
Strong cGMP and GDP behavior
Employee Value Proposition: Growth/ opportunity.
Red Flags:
No previous experience, inability to gown up per requirements for manufacturing and support on the floor operations.
Interview process:
Virtual 3 interviews with some key players
We invite qualified candidates to send your resume to *****************************. If you decide that you're not interested in pursuing this position, please feel free to look at the other positions on our website ******************************* You are welcome to also share this opportunity with anyone you think might be interested in applying for this role.
Regards, 3KC Talent Acquisition Team
$52k-76k yearly est. Easy Apply 60d+ ago
Quality Assurance Associate II
Nygci
Quality assurance specialist job in Framingham, MA
NYGCI was founded in 2007 in New York State. Since then we have expanded our services footprint to 27+ states within USA, representing our service presence in more than 50% of US.We provide IT Professional Services to local, regional and global customers and reduce their IT risk and maximize their IT performance.
Job Description
The QA Product Release Associate is responsible for ensuring the safety, efficacy, purity, and quality of manufactured products through compliance with relevant quality standards, regulations and established procedures. They support the review of batch records, assemble and review batch files, support the completion of the annual product review, maintain and utilize Quality Assurance databases, utilize the SAP System, review documentation for compliance with relevant quality standards, relevant regulatory councils, and other regulatory requirements and perform administrative tasks.. Years of Experience: 3 - 6 Years
Shift Day
Work Schedule: 8:00-5:00
Additional Information
All your information will be kept confidential according to EEO guidelines.
$51k-74k yearly est. 1d ago
Showroom Quality Assurance Associate
Supply New England 3.2
Quality assurance specialist job in Attleboro, MA
Summary/Objective
The Showroom Quality Assurance Associate ensures that the kitchen and bath showrooms are maintained at high standards, supports the installation of displays, and provides post sale customer service to guarantee a positive showroom experience.
Wage: $25.00/hr-$27.00/hr
Essential Functions
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Showroom display installation & maintenance.
Demo and removal of showroom displays
Merchandising pieces
Cabinetry
Dry-fit plumbing fixture installs (pedestal sinks, toilets, faucets, etc)
Painting, drywalling & drywall repair
Wallpaper installation
Tile installation
Hanging display boards
Maintaining a variety of showroom lighting systems; sourcing and replacing lamps and parts
Additional tasks based on company needs
Travel to customer homes or job sites in New England to help with light service issues.
Assist with project management to accommodate more complex showroom installations.
Communication, scheduling, materials planning, etc.
Quality assurance by confirming all showroom installations meet brand standards.
Checking all displays are installed properly and undamaged.
Report defects or inconsistencies and work to resolve issues quickly.
Competencies
Communication
Computer literacy (email, Microsoft, internet search etc.)
Organizational skills
Time management
Customer service
Relates well to others
Problem Solving
Job related skills
Safety awareness
General knowledge of plumbing and electrical work
Good knowledge of carpentry; wood working, millwork, finish work
Required Education and Experience
High school diploma or GED
Experience with general “handyman” tasks
Clean driving record
Tile installation a plus
$25-27 hourly 5d ago
ICQA Associate II
Barrett Distribution Center 2.9
Quality assurance specialist job in Bridgewater, MA
The Position:The ICQA Associate II, reporting to the ICQA Manager/Supervisor, is responsible for inventory cycle counting and tracking and monitoring inventory within the warehouse. This position works Monday through Friday, from 8am- 4:30pm. Expectation also to work from the Franklin facility 1x per week.
The compensation for this position is $17.50/hour.
Your Day-to-Day:
Performs daily cycle counts as directed by Inventory Manager, Lead, or Supervisor.
Reports, troubleshoots, and resolves inventory discrepancies as directed; escalated to facility leadership as needed.
Verifies quantity on hand by opening cartons, bundles, and other containers to count items and/or weigh materials.
Researches, identifies, and documents root cause inventory discrepancies.
Audits inbound and outbound shipments to maintain inventory accuracy and quality.
Assists employees in following SOP procedures for inventory transactions.
Maintains product identification, location, and lot code accuracy in appropriate systems.
Reports verbally and in writing on inventory accuracy or discrepancies
Assists with monitoring and controlling inventory integrity.
Works on special projects affecting inventory as directed by the customer.
Utilizes Barrett's Powered Industrial Vehicles (PIV) to complete necessary duties.
Barrett PIV Certification is required within the first 30 days (or as dictated by facility need); certification must remain in good standing.
Performs other duties as assigned.
What You Bring to the Table:
High school diploma/GED preferred.
Forklift certification strongly preferred.
Minimum of one (1) year's experience as a cycle counter in a warehouse/distribution setting. Experience conducting process audits and audits on inbound and outbound shipments.
Knowledge of Lean concepts preferred.
Working knowledge of warehouse management systems preferred.
Ability to read, write, and communicate effectively in English (Bilingual Spanish/English skills preferred). Basic math skills - add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
Must be able to interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
Experience must demonstrate excellent verbal and written communication skills, as well as organizational skills and attention to detail.
Excellent time management skills with a proven ability to meet deadlines and the ability to function well in a high-paced and, at times, stressful environment.
The above statements are intended to describe the general nature and level of work performed by employees assigned to this classification. They are not to be construed as an exhaustive list of all job duties performed by the personnel so classified.
Barrett Distribution Centers is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, retaliation, national origin, ancestry, sexual orientation, gender, gender identity/expression, mental or physical disability, genetic information, choice of health insurance, marital status, age, veteran status or any other basis protected by law.
$17.5 hourly 22d ago
QC Investigations Specialist
JMD Technologies Inc.
Quality assurance specialist job in Boston, MA
Title: QC Investigations Specialist
Employment Type: Contract
Status: Accepting Candidates
About the role
This role supports real-time manufacturing operations by leading investigations, resolving on-floor issues, and ensuring high-quality documentation. You'll partner closely with manufacturing, QC, materials, and facilities teams to maintain operational continuity and compliance.
Key Responsibilities
• Triage manufacturing issues and lead analytical investigations and root cause analysis.
• Write clear, compliant quality documentation including deviations and CAPAs.
• Coordinate with SMEs to determine immediate actions, containment, and impact assessments.
• Interpret data to support structured problem-solving and continuous improvement.
• Provide technical operations support across manufacturing and QC functions.
Qualifications
• 6+ years pharmaceutical or biotech manufacturing experience.
• 4+ years analytical investigation and QC-focused experience.
• Strong background in RCA, deviation management, and GxP documentation.
• Ability to interpret analytical data and think scientifically under time-sensitive conditions.
• Experience partnering cross-functionally with manufacturing, QC, materials, and facilities teams.
Compensation (MA Pay Transparency):
• Estimated hourly range: $50-$55/hr (W-2).
• Final rate within this range will be based on skills, experience, and interview results.
$50-55 hourly 4d ago
Food Safety Quality Assurance Coordinator
LSG Sky Chefs 4.0
Quality assurance specialist job in Boston, MA
Job Title: Food Safety Quality Assurance Coordinator Salary Range: $18.00 - 25.00 per hour
About us
LSG Sky Chefs is one of the world's largest airline catering and hospitality providers, known for its outstanding reputation and dynamic approach in the industry. Voted "Airline Caterer of the Year in North America" for 2023 and 2024, we are committed to excellence and innovation, driven by the dedication and expertise of our talented employees. Our team members are the heart and soul of our success, consistently delivering exceptional culinary experiences and outstanding service to our clients and their passengers across North and Latin America.
Role Purpose Statement
Primary responsibility is to maintain the "Global Quality System" of LSG Sky Chefs to ensure the Customer Service Center (CSC) is in compliance with customer, Federal Drug Administration (FDA), US Department of Agriculture (USDA), and Seafood Hazard Analysis and Critical Control Points (HACCP) plans including USDA and FDA regulatory standards.
Main Accountabilities
Maintain and initiate all recordkeeping and key performance indicators pertinent to the Quality Department and GQS to include, but not limited to Food Safety, Sanitation, Regulatory Agencies (County Health, State Health Dept. and FDA), internal customers and airline customers
Daily monitor of Good Manufacturing Practices (GMPs) for compliance
Verify of coolers and freezer room temperature for compliance
Perform environmental swabs and microbiological sampling, submittal to local laboratory for analysis
Obtain Chef Table samples to verify compliance to specification
Assist the Quality Manager in specific training and daily initiatives addressing quality, food safety, and sanitation issues to drive process improvements
Conduct work station inspections to verify compliance (gold standard verification, specs, sanitizer, food temperatures, HACCP documentation, phf set-up)
Conduct portion control weight compliance to specifications
Conduct inspection checks (dispatch, galley, non-bonded, bonded, equipment)
Verify Hazard Analysis and Critical Control Points (HACCP) logs and other documents are accurately completed on a daily basis
Create charts, trending reports, training materials and visuals
Maintain, monitor standards and train employees in compliance to the Regulated Garbage Standards to meet USDA requirements
Supports the Jump-off (commissary) locations with oversight
Train hourly employees as needed
Perform other tasks as requested
Knowledge, Skills and Experience
High School Diploma or equivalent
Proficient in using computer and basic software such as Microsoft, create and maintain trending charts, SOP's, use of calculator, weight scales, and thermometers, metal detector, ATP testing equipment, mechanical food portioning and processing equipment.
Previous food industry and quality assurance experience a plus
Ability to work in cold environment (
Ability to work with minimum to no supervision, act in liaison of the Supervisor, self-starter, and problem solver.
Ability to lift/push a minimum of 25 lbs.
Strong mathematical, analytical, verbal, written, interpersonal and organizational skills
Ability to work in fast paced environment with large groups
Must be flexible to work weekends/holidays
LSG Sky Chefs is an EEO and Affirmative Action Employer of Women/Minorities/Veterans/Individuals with Disabilities.
$18-25 hourly 17h ago
Learn more about quality assurance specialist jobs
How much does a quality assurance specialist earn in Warwick, RI?
The average quality assurance specialist in Warwick, RI earns between $57,000 and $123,000 annually. This compares to the national average quality assurance specialist range of $41,000 to $97,000.
Average quality assurance specialist salary in Warwick, RI
$84,000
What are the biggest employers of Quality Assurance Specialists in Warwick, RI?
The biggest employers of Quality Assurance Specialists in Warwick, RI are: