798 Results for

Quality Assurance Jobs in Newport, RI

Jobs

Providence, RI

$75,000–$105,000 / year
Full time

li class="___ccc16d0 fje8fi8 f1ng9h0j f1bwykku f18jd3zf">Measure and report supplier KPIs, driving corrective actions and improvements.

Lead supplier quality performance, risk reduction, and continuous improvement initiatives.

1 day ago

Smithfield, RI

$55–$65

Kforce has a client in Smithfield, RI that is seeking a Systems Analyst who will be a key member to gather & document business requirements, helping with current state analysis of our systems, helping define our technology solution, and partnering with QA in test case preparation. Employee pay is based on factors like relevant education, qualifications, certifications, experience, skills, seniority, location, performance, union contract and business needs.

8 days ago

Providence, RI

Remote

$92,300–$166,850

June 8, 2026

For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at LeidosCareersFraud@leidos.com.

21 days ago

Pawcatuck, CT

Yale New Haven Health includes Yale New Haven, Bridgeport, Greenwich, Lawrence + Memorial, and Westerly hospitals; several specialty networks; and Northeast Medical Group, a physician-led multi-specialty group with over 1,000 physician. As a valued member of our team, you will:

Conduct comprehensive health assessments, including obtaining detailed medical histories, performing physical examinations, and ordering/interpreting diagnostic tests.

1 day ago

Fall River, MA

li>Educate patients and caregivers on home exercise programs, proper body mechanics, injury prevention strategies, and self-management techniques to promote long-term functional recovery. Working in settings such as hospitals, clinics, and rehabilitation centers, they create personalized, evidence-based treatment plans using exercise and manual therapy to help patients recover and become independent.

4 days ago

Coventry, RI

This role provides QA oversight of manufacturing activities, analytical method development, stability programs, cleaning verification, and key quality systems supporting early-phase clinical API supply. Pharmaron is a global leader in life sciences services, supporting drug discovery through clinical and commercial manufacturing across small molecules, biologics, and advanced modalities.

30+ days ago

West Greenwich, RI

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Preferred Qualifications: Demonstrated experience leading enterprise risk management within GxP environments, including development of risk frameworks, predictive KPIs, escalation governance models, and cross-functional mitigation strategies to proactively identify and reduce quality and supplier-related risks.

20 days ago

Pawtucket, RI

Remote

$100,000–$120,000 / year

p>Four-year degree in technical or science discipline required 4-6 years related experience in a regulated environment, preferably medical device is required 1-3 years experience in supervisory/management role is required.

The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally.

30+ days ago

Providence, RI

As the world's only end-to-end professional services firm focused on MedTech, we take clients' Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting. What You Will Do: Perform day‑to‑day maintenance and administration of the QMS, including eQMS data entry, document updates, records management, monitoring system due dates, and responding to quality‑related requests from staff and project teams.

30+ days ago

This role demands strong analytical judgment, a self-directed mindset, and the ability to read, interpret, and apply investor and regulatory guidelines (FHA, VA, Fannie Mae, Freddie Mac, RESPA, Regulation X, CFPB, etc.) to identify errors, gaps, and risks within the business line.

Read, interpret, and apply investor guides (Fannie, Freddie, FHA, VA, USDA, GNMA) and regulatory requirements (RESPA, Reg X, Reg Z, UDAAP, SCRA, FDCPA) to evaluate business line performance.

12 days ago

West Greenwich, RI

$25–$29 / hour

We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.

Review logbooks paper-based and electronic particle-generating forms pest control sighting forms and periodic pest control monthly/quarterly reports RT reports and other GMP documentation.

5 days ago

Bristol, Bristol

£40,000–£42,000

The Quality Assurance Manager will play a pivotal role in ensuring the delivery of robust, fair, and highquality assessments for apprentices across multiple sectors, maintaining strict compliance with regulatory . We're a friendly, DfE accredited, Ofsted outstanding training company providing apprenticeships, professional development and the DfE's 'Golden Thread' (trainee teachers to school Executive Leaders).

30+ days ago

Johnston, RI

The Collections & Recovery QC Analyst is an experienced Quality Control professional who operates independently, applies strong analytical judgment, and contributes meaningfully to QC program effectiveness. History of strong performance driven by being self-motivated, taking initiative to turn ideas into actions, and producing significant output at a high level.

30+ days ago

Fall River, MA

$176,659–$229,427 / year

li>Develop and oversee a competency-based QA training program including but not limited to employee QS training, cGMP, Document Control, deviation reporting and documentation guidelines; assist other area managers in the development of competency-based department specific training programs; oversee all training documentation for the facility including employee training files and training modules.

The Director, Quality Assurance at Celldex Therapeutics will lead and oversee all GMP Quality Assurance operations for the Fall River site, ensuring compliance with FDA, cGMP, and international regulatory requirements across manufacturing, testing, product disposition, training, audits, and quality systems.

30+ days ago

Starting as a hardware supply store during the California Gold Rush and eventually assisted in the birth of the aerospace industry in Southern California by providing aircraft aluminum to early aerospace pioneers like Lindbergh, Douglas and Lockheed. The Quality Assurance Technician will participate in the customer contract review process, support Internal Audit Program, promote the implementation of Corrective Actions, revise technical documents, analyze inspection data, and report results to Management.

30+ days ago

West Greenwich, RI

Position Overview: In this critical role, you will serve as a Plant Quality Assurance (PQA) professional, providing on-the-floor quality oversight for Facilities and Engineering (F&E), Process Development, Incoming Quality Assurance (IQA), and Manufacturing operations. • Demonstrated experience utilizing enterprise systems such as Maximo, OEFM, MES, and Veeva Vault (CDOCS/DQMS) to support quality oversight, documentation management, and manufacturing execution processes.

15 days ago

West Greenwich, RI

$24–$25 / hour

em>Consent to Communication and Use of AI Technology: By submitting your application for this position and providing your email address(es) and/or phone number(s), you consent to receive text (SMS), email, and/or voice communication whether automated (including auto telephone dialing systems or automatic text messaging systems), pre-recorded, AI-assisted, or individually initiated from Aditi Consulting, our agents, representatives, or affiliates at the phone number and/or email address you have provided. You represent and warrant that the email address(es) and/or telephone number(s) you provided to us belong to you and that you are permitted to receive calls, text (SMS) messages, and/or emails at these contacts.

15 days ago

Fall River, MA
Our assortment of superior fresh and value-added seafood is unmatched, and our focus is on inspiring, educating, and supporting customers with specialty seafood solutions that elevate menus and retail categories.
Experience and understanding of food ingredients, nutritional labels, allergens, and governmental regulations set forth by the USDC, USDA, and FDA preferred.
19 days ago

West Greenwich, RI
$26–$27.84 / hour
In this critical role, you will serve as a Plant Quality Assurance (PQA) professional, providing on-the-floor quality oversight for Facilities and Engineering (F&E), Process Development, Incoming Quality Assurance (IQA), and Manufacturing operations.
Demonstrated experience utilizing enterprise systems such as Maximo, OEFM, MES, and Veeva Vault (CDOCS/DQMS) to support quality oversight, documentation management, and manufacturing execution processes.
15 days ago

North Kingstown, RI
p>System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.
Provide feedback on errors and support production in inspection and segregation of non-conforming products.
25 days ago

Fall River, MA
p>About InvaGen Pharmaceuticals, a Cipla subsidiary: InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.
30+ days ago

West Greenwich, RI
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients.
19 days ago

RI
This role is responsible for ensuring compliance with AS9100, ISO 9001, and applicable regulatory requirements while driving continuous improvement across manufacturing, inspection, supplier quality, and customer satisfaction.
The ideal candidate will be a hands-on leader with strong aerospace quality experience who can balance compliance, execution, and process improvement in a fast-paced, regulated manufacturing environment.
30+ days ago

New
New Bedford, MA
$112,000–$154,000 / year
Placement in the range depends on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, relevant experience, skills, seniority, performance, shift, travel requirements, and business or organizational needs and may change over time. Reporting to the Quality Director, this person will be responsible for identifying opportunities for continuous improvement, formulating corrective and preventive actions, and working to implement those actions to improve quality levels and regulatory compliance.
6 days ago

Cranston, Rhode Island
p>Responsibilities include but are not limited to:
Supports development and maintenance of quality systems by writing quality plans, including dimension requirements and inspection specifications, by analyzing blueprints to determine critical dimensions.
Performs hydro inspection, final inspection, in-process inspection and non-destructive examinations (NDEs) as needed within production cells and/or Engineering Lab.
30+ days ago

MA
$19–$22 / hour
p>Qualifications Being able to work as needed in a group and individual setting Ability to visually inspect parts and distinguish between conforming and nonconforming parts per guidelines Ability to make decisions by self and support with documentation Effective written and verbal communication skills with team members, departments, and vendors Strong organization skills Ability to multi-task and manage stressful situations Able to prioritize tasks in an efficient manner in order to meet deadlines Ability to perform mathematical calculations as necessary Strong commitment toward quality, safety, and continuous improvement Preferred: Knowledge of Window Quality specifications Preferred: Knowledge of Home Construction. 2 - 5 years Quality OR Manufacturing experience in a non-electronics/non-food setting Experience using Measuring Equipment (Tape Measure Required and Calipers preferred) Basic knowledge in use of inspection equipment and reading technical drawings Basic knowledge of quality systems and tolerances (+/-, passible defects, etc) Strong interest in process improvement and problem solving Strong computer skills (Microsoft Word and Excel) Must be able to read, write, and speak English at an intermediate level.
30+ days ago

Fall River, MA
$66,300–$86,000 / year
p>About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants.
Knowledge and experience with analytical laboratory activities in areas such as active pharmaceutical ingredients (API), drug products, analytical development, Quality Control (QC), Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP)/Good documentation Practices (GDP), etc.
30+ days ago

Fall River, MA
$26–$33 / hour
p>About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.
30+ days ago

New
Fall River, MA
$21–$26 / hour
p>About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.
5 days ago

New
Fall River, MA
h5>Please read the California Employee Privacy Notice ("CA Privacy Notice") regarding Sunnyside* and its affiliate Cresco Labs' policies pertaining to the collection, use, and disclosure of personal information. Be aware that fraudulent job offers and correspondence may appear legitimate: they may feature a Cresco Labs logo, they may appear to originate from an official-looking email address or web site, or they may be sent by individuals purporting to represent Cresco Labs or an entity which includes the word Cresco Labs in its name.
5 days ago

Fall River, MA
Be aware that fraudulent job offers and correspondence may appear legitimate: they may feature a Cresco Labs logo, they may appear to originate from an official-looking email address or web site, or they may be sent by individuals purporting to represent Cresco Labs or an entity which includes the word Cresco Labs in its name. With dozens of locations nationwide, our owned and operated Sunnyside dispensaries provide a welcoming, positive, judgement-free place to shop for anyone at any point on their cannabis journey.
7 days ago

New Bedford, MA
$112,000–$154,000 / year
Part time
Placement in the range depends on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, relevant experience, skills, seniority, performance, shift, travel requirements, and business or organizational needs and may change over time. Reporting to the Quality Director, this person will be responsible for identifying opportunities for continuous improvement, formulating corrective and preventive actions, and working to implement those actions to improve quality levels and regulatory compliance.
7 days ago

Providence, RI
Required Skills and Qualifications: Bachelor's degree in computer science, engineering, or related field 3+ years of experience in software quality assurance and automated testing Proficiency with automation tools (e.g., Selenium, Cypress, or similar) Experience with code review tools and CI/CD pipelines Strong understanding of regression testing and release management Familiarity with security testing practices and tools Excellent analytical and problem-solving skills Effective communication and teamwork abilities. This position is responsible for managing code review acceptance, leading regression testing throughout the software development life cycle, staging releases before production, and ensuring ongoing security testing of the ISPRI platform.
30+ days ago

Warwick, RI
Remote
$50,000–$60,000 / year
li>
Responsibility for problem solving, assessing processes and issues, and collaborating with staff and providers to develop solutions resulting in efficient and functional workflows for end users of our software application. If you're looking to make a change and put your administrative, reporting, and data analytics skills to use, don’t miss this opportunity to take your career to the next level and join a growing, well-regarded organization that truly cares for their employees and clients!
8 days ago

Providence, RI
$19.03–$31.39 / hour
Interpersonal skills to consult with other staff members Analytical and advanced numerical skills to perform complex calculations and to evaluate and resolve data discrepancies Demonstrated knowledge and skills necessary to provide care to patients throughout the life span, with consideration of aging processes, human development stages and cultural patterns in each step of the care process Work Environment and Physical Requirements: Exposed to low level of ionizing radiation while handling radioactive substances. Participate in physics related aspects of research projects performing such technical duties as setting up equipment, taking measurements and recording data, as assigned Attends meetings and conferences and reads current scientific literature to maintain and enhance professional expertise MINIMUM QUALIFICATIONS: Basic Knowledge: Bachelor's Degree in physics, or related science or enrolled in undergraduate physics program.
30+ days ago

West Warwick, RI
Job Function: Performs visual, dimensional and functional inspection of packaging components, in-process material and finished products as part of the manufacturing process. Locates raw material, packaging components or finished product by IC number or production date using current inventory control software.
30+ days ago

Rhode Island
Interpersonal skills to consult with other staff members Analytical and advanced numerical skills to perform complex calculations and to evaluate and resolve data discrepancies Demonstrated knowledge and skills necessary to provide care to patients throughout the life span, with consideration of aging processes, human development stages and cultural patterns in each step of the care process Work Environment and Physical Requirements: Exposed to low level of ionizing radiation while handling radioactive substances. Participate in physics related aspects of research projects performing such technical duties as setting up equipment, taking measurements and recording data, as assigned Attends meetings and conferences and reads current scientific literature to maintain and enhance professional expertise MINIMUM QUALIFICATIONS: Basic Knowledge: Bachelor’s Degree in physics, or related science or enrolled in undergraduate physics program.
30+ days ago

East Providence, RI
p>• Bachelor's Degree (engineering or technical preferred) from an ABET accredited program • 6-10 years quality assurance-related experience • Proficient in Microsoft Office: Excel, Word, and PowerPoint • Experience working in an ISO 90000 manufacturing environment or equivalent • Demonstrated intermediate problem-solving skills - Root Cause Analysis/Problem Solving Methods (8-D, PDCA, DMAIC) • Demonstrated advanced problem-solving and training skills (Certified 6S Master Black Belt or equivalent) • Demonstrated knowledge of advanced Lean principles and methods (Certified Lean/6-Sig, Value Stream Mapping, RIE, Status Display) • Demonstrated basic understanding and training in at least three of the following areas: • Probability and Statistics • Industrial statistics (Cpk, MSA, SPC) • QA Tools (PPAP, FMEA, Control Plans) • Design of Experiments • Able to read, understand, and interpret technical drawings/documentation from three and able to create technical drawings/documentation in at least one of the following disciplines: • Pneumatics • Data acquisition/Gauging • Mechanical Design • Electronics and sensors • Chemical formula preparation.
• Working knowledge of Injection Molding equipment and processes • Working knowledge of machined part equipment and processes • Working knowledge of advanced Lean principles and methods (Value Stream Mapping, RIE, Status Display, 6S, Continuous Flow) • Certified Six Sigma Green Belt/Black Belt • Certified quality engineer/Certified manager of quality/Organizational Excellence (CMQ/OE) • Demonstrates a passion and a responsibility for consumer • Exhibit a passion for the company's Essence, Global Imperatives, Corporate Direction • Desire to own decisions and take responsibility for outcomes • Willingness to continually embrace personal and professional development • Demonstrated exceptional written and oral communication skills • Experience in quality management systems • Experience in quality system audits.
30+ days ago

Warwick, RI
$50,400–$72,000 / year
Gainwell Technologies defines "wages" and "wage rates" to include "all forms of pay, including, but not limited to, salary, overtime pay, bonuses, stock, stock options, profit sharing and bonus plans, life insurance, vacation and holiday pay, cleaning or gasoline allowances, hotel accommodations, reimbursement for travel expenses, and benefits.
Facilitator for various audits including but not limited to annual independent third-party audit of all operational practices; bi-annual PERM (federal CMS) audit of system and business processes; annual false claims act compliance audit; other periodic internal and external quality audits.
8 days ago

Coventry, RI
p>find description in this url https://jobs.bostonscientific.com/job/Coventry-QA-Associate-Documentation-I-RI-02816/1394272400/.
30+ days ago

W. Warwick, RI
The employee frequently is required to use hands, hands to finger, handle, or feel objects, tools or controls and talk or hear. The employee is occasionally required to stand; walk; reach with hands and arms; and stoop, kneel, or crouch.
30+ days ago

Fall River, MA
$86,000–$113,500 / year
p>About InvaGen Pharmaceuticals, a Cipla subsidiary: InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.
30+ days ago

Fall River, MA
$76,000–$103,000 / year
p>Job Title: QA Associate FLSA Classification: Full-Time, Exempt Professional Work Location: Fall River, MA Work Hours: General: 8:00AM - 5:00PM (May vary based on business needs) Reports To: Site Quality Assurance Head Salary Range: $76,000 - $103,000 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. CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.) About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants.
30+ days ago

Providence, RI
As the world's only end-to-end professional services firm focused on MedTech, we take clients' Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.
Lead risk management for novel and existing medical devices, including risk management plans and reports, hazard analyses and use, design, and process Failure Mode & Effects Analysis (FMEA).
29 days ago

Bristol, Bristol
£47,410–£54,210
Ensure National Highways reputation is maintained throughout delivery of projects by delivering best practice customer and stakeholder communications Proactively manage interaction with communities, stakeholders, transport operators, road users and businesses. We address over 39,000 customer enquiries every month, plan and deliver all maintenance activities on the network, drive efficiencies and improvements across our systems and roads, and respond to incidents across 4,500 miles of motorways and major A-roads that we manage.
30+ days ago

New Bedford, MA
$107,896–$134,765 / year
Partnering cross-functionally with Manufacturing, R&D, Supply Chain, and external suppliers, the Senior Engineer provides technical expertise in root cause analysis, corrective and preventive actions, and new product introductions.
The Senior Engineer, Central Quality & Quality Control plays a critical role in driving excellence across manufacturing operations and supplier networks by ensuring consistent product performance and compliance with Acushnet Company Quality System requirements.
30+ days ago

New Bedford, Massachusetts
Please click here for more details.
The Senior Engineer, Central Quality & Quality Control plays a critical role in driving excellence across manufacturing operations and supplier networks by ensuring consistent product performance and compliance with Acushnet Company Quality System requirements.
30+ days ago

Hope Valley, RI
At Wood River Health the Quality Improvement (QI) Specialist supports organizational quality improvement initiatives by collecting, analyzing, and distributing clinical outcomes data for internal and external reporting, as well as supporting internal and external audits. This role assists with routine quality-related activities, including data entry, electronic health record (EHR) review, and the administration of quality assurance and compliance processes.
30+ days ago

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Quality Assurance Jobs in Newport, RI

Supplier Quality Engineer - Medical Device - Providence, RI Michael Page USA

Systems Analyst Kforce Inc.

Substation Senior Civil/Structural Engineer Leidos

APP| Primary Care Outpatient | New London, CT Yale New Haven Health

Travel Physical Therapist (PT) Fusion Medical Staffing

Sr. Quality Assurance (QA) Specialist II- Early Phase / Kilo Lab Pharmaron Beijing Co Ltd

QA Specialist Amgen Inc

Quality Assurance Quality Control Manager Zoll Data Systems, Inc.

Quality Assurance Specialist 2 Veranex Inc

QA QC Associate Citizens Financial Group Inc

Quality Assurance Specialist Actalent Inc

Quality Assurance and Standards Manager Supporting Education Group

Consumer QA QC Associate Citizens Financial Group Inc

Director, Quality Assurance Celldex Therapeutics Inc

Quality Assurance Technician Ducommun Inc

Quality Assurance Senior Associate Aequor Technologies LLC

Quality Assurance Senior Associate Aditi Consulting

Quality Assurance Tech Raw Seafoods, Inc.

Quality Assurance Senior Associate #26-14105 US Tech Solutions, Inc.

Quality Assurance Auditor System One

QA Operations Specialist Cipla Ltd

Sr Associate QA - Days Amgen Inc

Sr Associate QA - Nights Amgen Inc

Quality Assurance Manager AstroNova Inc

Quality Assurance Manager Atkore Inc

Quality Assurance Technician Taco Family of Companies

Manufacturing Quality Assurance Technician 2nd Shift Cornerstone Building Brands Inc

Analytical QA Associate I Cipla Ltd

QA Inspector II - 2nd Shift Cipla Ltd

QA Inspector I - 1st Shift Cipla Ltd

Quality Assurance Technician Cresco Labs

Quality Assurance Technician Cresco Labs Inc

Quality Assurance Manager AFC Cable Systems, Inc

QA Engineer EpiVax Inc

Clinical Data and QA Coordinator Northeast Family Services

Quality Assurance Technician IMRT Brown University Health

QA Tech - 3rd shift (11pm to 7am) Bradford Soap works Inc

Quality Assurance Technician IMRT RIH Rhode Island Hospital

Manager, Quality Assurance Nordson Corp

Manager Plant Quality Assurance Amgen Inc

Healthcare Operations Quality Assurance (Hybrid Warwick, RI) Gainwell Technologies LLC

QA Associate Documentation I Boston Scientific Corp

QA Inspector 1 AstroNova Inc

QA Compliance Manager Cipla Ltd

QA Associate IT Cipla Ltd

Sr Design Assurance Engineer Veranex Inc

Construction Assurance Manager National Highways

Senior Engineer, Central Quality & Quality Control | Titleist Acushnet Holdings Corp

Senior Engineer, Central Quality & Quality Control | Titleist Acushnet Company

Quality Improvement (QI) Specialist Wood River Health Services Inc

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