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Qa Validation Engineer Jobs in Rhode Island (NOW HIRING)

Amgen

Manager QA - Nights

West Greenwich, RI · On-site

... validation protocols and reports for manufacturing processes, and approving environmental ... Bachelor's Degree in Life Sciences, Engineering or related field * 6+ years of quality assurance or ...

Amgen, Inc.

Manager QA - Nights

West Greenwich, RI · On-site

... validation protocols and reports for manufacturing processes, and approving environmental ... Bachelor's Degree in Life Sciences, Engineering or related field * 6+ years of quality assurance or ...

Syntricate Technologies

Python, PySpark and GCP

Woonsocket, RI · On-site

$109K - $131K/yr

The role involves working on data engineering solutions, leveraging best practices and industry ... Syntricate Technologies offers quality assurance, validation, regulatory, business analysis, and ...

Aptiv PLC

Quality Engineer

Warwick, RI · On-site

$72K - $93K/yr

Serve as the primary quality assurance resource to department supervisor(s) for problem ... Participate in internal and external training programs to maintain knowledge of validation ...

Aptiv PLC

Quality Engineer

Warwick, RI · On-site

$90 - $120/hr

Serve as the primary quality assurance resource to department supervisor(s) for problem ... Participate in internal and external training programs to maintain knowledge of validation ...

Aptiv

Quality Engineer

Warwick, RI · On-site

$72K - $93K/yr

Serve as the primary quality assurance resource to department supervisor(s) for problem ... Participate in internal and external training programs to maintain knowledge of validation ...

Syntricate Technologies

Helpdesk support

Providence, RI · On-site

$20.25 - $27.25/hr

Syntricate Technologies offers quality assurance, validation, regulatory, business analysis, and project management services. Founded in 2004, the company is headquartered in Boston, USA, with a team ...

Bradford Soap Works Inc

Quality Engineer

West Warwick, RI · On-site

$69K - $90K/yr

Support new product introductions (NPI), validation protocols (IQ/OQ/PQ), and process changes and ... quality assurance experience in a manufacturing environment. * Experience with audits ...

Bradford Soap Works Inc

Quality Engineer

West Warwick, RI · On-site

$69K - $90K/yr

Support new product introductions (NPI), validation protocols (IQ/OQ/PQ), and process changes and ... quality assurance experience in a manufacturing environment. * Experience with audits ...

Amgen

Sr Specialist QA - Compliance

West Greenwich, RI · On-site

$89K - $123K/yr

... validations, document management, and data integrity controls. * Identify gaps, risks, or weak ... Bachelor's Degree in Life Sciences or Engineering * Experience with leading and/or participating in ...

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All JobsQa Validation Engineer JobsQa Validation Engineer Jobs in Rhode Island

Qa Validation Engineer information

See Rhode Island salary details

$22

$50

$76

How much do qa validation engineer jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for qa validation engineer in Rhode Island is $50.92, according to ZipRecruiter salary data. Most workers in this role earn between $38.61 and $61.92 per hour, depending on experience, location, and employer.

What is a QA Validation Engineer?

QA Validation Engineers are professionals responsible for ensuring that products, systems, or software meet specified quality and regulatory standards before they are released or deployed. They design and execute validation protocols, document results, and identify any issues or non-conformities during the testing process. Their role is crucial in industries like pharmaceuticals, manufacturing, and software, where compliance and reliability are essential. QA Validation Engineers collaborate closely with development, production, and regulatory teams to ensure that products are safe, effective, and meet all necessary guidelines.

How does a QA Validation Engineer typically collaborate with cross-functional teams during product development?

As a QA Validation Engineer, you’ll work closely with development, regulatory, and operations teams to ensure products meet quality and compliance standards. You’ll participate in project meetings, review technical documentation, and provide input on test strategies and validation protocols. Effective communication and problem-solving are essential, as you may need to clarify requirements, address issues found during validation, and coordinate testing activities. This collaborative environment helps ensure that products are released on schedule and comply with industry regulations.

What are the key skills and qualifications needed to thrive as a QA Validation Engineer, and why are they important?

To thrive as a QA Validation Engineer, you need a solid understanding of quality assurance methodologies, validation protocols, and a relevant technical degree such as in engineering or life sciences. Familiarity with industry regulations (such as FDA or ISO standards), validation management software, and documentation tools is typically required. Attention to detail, analytical thinking, and strong communication skills help you excel in identifying compliance gaps and collaborating with cross-functional teams. These skills and qualities are crucial to ensure products meet regulatory requirements and maintain high standards of quality and safety.

What is the difference between Qa Validation Engineer vs QA Tester?

AspectQa Validation EngineerQA Tester
CertificationsISTQB, CQE, or similarISTQB Foundation, CSTE
Work EnvironmentRegulatory, validation-focused industries like pharma, biotechSoftware development, IT, web applications
ResponsibilitiesValidating systems, ensuring compliance, writing validation protocolsExecuting test cases, identifying bugs, reporting issues

While both roles focus on quality assurance, Qa Validation Engineers primarily work on validating systems for compliance and regulatory standards, often in industries like pharmaceuticals. QA Testers concentrate on testing software functionality and identifying bugs during development. The roles overlap in testing skills but differ in scope and industry focus.

Are QA Validation Engineers in demand?

QA Validation Engineers are in demand across industries such as pharmaceuticals, biotech, and manufacturing, where regulatory compliance and quality assurance are critical. The role requires knowledge of validation processes, testing protocols, and often involves working with tools like GxP standards and validation software, making experienced professionals highly sought after.

Do validation engineers make good money?

Validation engineers, including QA validation engineers, typically earn competitive salaries that vary by industry, experience, and location. They often require knowledge of testing tools, validation protocols, and quality standards, which can influence compensation levels. Overall, validation engineering is considered a well-paying profession within quality assurance and engineering fields.

What are popular job titles related to Qa Validation Engineer jobs in Rhode Island?

For Qa Validation Engineer jobs in Rhode Island, the most frequently searched job titles are:

What job categories do people searching Qa Validation Engineer jobs in Rhode Island look for?

The top searched job categories for Qa Validation Engineer jobs in Rhode Island are:

Qa Validation Engineer jobs near you
Infographic showing various Qa Validation Engineer job openings in Rhode Island as of August 2026, with employment types broken down into 87% Full Time, 9% Part Time, and 4% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $105,915 per year, or $50.9 per hour.

Quality Assurance Associate I (Cumberland, RI)

CEDENT

Cumberland, RI

Full-time

Re-posted 12 days ago

Job description

SUMMARY/OBJECTIVE This position supports activities of the Quality Assurance Department regarding pharmaceutical manufacturing, testing and packaging to ensure compliance with all relevant pharmaceutical regulatory requirements: FDA, GMP. Provides QA oversight to operations under direction of the QA Manager. Provides review, impact/risk assessment analysis, detailed improvement plans for change controls, deviations, investigations and CAPA.

Adheres to Client compliance initiatives, including following all quality and division/company policy requirements. Helps to ensure that all Client products meet quality requirements by supporting all assigned quality aspects of product approval. The QA Associate II/III independently conducts quality assurance audits of production records (manufacturing, analytical and quality control records) and facility records assuring company standards are maintained and product integrity is preserved.

RESPONSIBILITIES 1. Provide support to GMP investigations, validation documentation review and approval, identify gaps within existing Quality Systems and propose solutions for functional management; 2. Participates/leads internal/external audits, prepare and issue audit reports.

Recommend remediation actions and follow up on implementation of the plan. 3. Supports resolution of technical and compliance issues/gap analysis.

4. Aides implementation of Quality Systems/System Improvements. 5.

Supports and assists with Quality systems-related training, including compliance with cGMP and SOPs. 6. Interface with key quality, manufacturing, customers and coordinate documentation impacting quality areas.

7. Review/approval of all cGMP documents generated across site to include (but not limited to): SOPs, technical reports, validation documents, QA assessment, APRs, audit documents, change control, deviation & document revisions, etc. 8.

Participates in activities associated with primary batch record review, non-conformances investigation and CAPA. 9. Work in coordination with regulatory affairs group in support of ANDA submissions.

10. Provides QA review/approval of all cGMP documents associated with manufacture of product. 11.

Communicates with contractors and internal manufacturing/technical groups regarding compliance and quality issues (i.e., batch documentation, investigations, timelines and data related issues). 12. Authors or revises SOPs as necessary

13. Actively engaged in the training of staff with lesser experience or knowledge of quality assurance processes. Educate and instruct QA and plant personnel in quality best practices for sampling, labeling, good documentation practices, equipment sanitation.

Confirm these procedures are being adhered to, taking corrective actions when non-conformances are observed. 14. Routinely provide input to quality and operations management for better operational procedures to improve overall efficiency and regulatory compliance.

15. Assist in development of special department projects and work in conjunction with quality management. 16.

Other duties as assigned. COMPETENCIES 1. Project Management 2.

Technical Capacity. 3. Discretion.

4. Problem Solving/Analysis. 5.

Decision Making. 6. Communication Proficiency.

7. Collaboration Skills. 8.

Learning Agility 9. Managing Changing Priorities POSITION TYPE/EXPECTED HOURS OF WORK This is a full-time position requiring 40 or more hours of work per week.

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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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