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Quality Control Contract Jobs in Rhode Island (NOW HIRING)

Pharmaron

QC Informatics Specialist

Coventry, RI · On-site

$80K - $120K/yr

Computer System Validation/QC Informatics Specialist Salary Range: $80,000 - $120,000/yr ... Location: Coventry, RI (On-site) About Pharmaron Pharmaron is a global contract research and ...

Ducommun Incorporated

Quality Engineer

Warren, RI · On-site

$70 - $90/hr

Performs Customer Contract Review to ensure compliance with regulatory, industry, and customer ... Set quality control compliance objectives to achieve targets (Cost of Poor Quality, Scrap Rates ...

Ducommun, Inc.

Quality Engineer

Warren, RI · On-site

$71K - $92K/yr

Communicate to Management the impact of process variation. - Performs Customer Contract Review to ... process control, improve product quality and conformance, and ensure inspection equipment is ...

Ducommun

Quality Engineer

Warren, RI · On-site

$71K - $92K/yr

Communicate to Management the impact of process variation. - Performs Customer Contract Review to ... process control, improve product quality and conformance, and ensure inspection equipment is ...

Ducommun

Quality Engineer

Warren, RI

$71K - $92K/yr

... control, identify root causes of process deviation, and implement corrective actions to reduce ... Communicate to Management the impact of process variation. - Performs Customer Contract Review to ...

Ducommun

Quality Engineer

Warren, RI

$71K - $92K/yr

... control, identify root causes of process deviation, and implement corrective actions to reduce ... Communicate to Management the impact of process variation. - Performs Customer Contract Review to ...

Aptiv PLC

Quality Engineer

Warwick, RI · On-site

$72K - $93K/yr

Design and implement methods for process control, process improvement, testing and inspection ... Review customers purchase orders, contracts and change requests and ensure that the necessary ...

Aptiv

Quality Engineer

Warwick, RI · On-site

$72K - $93K/yr

Design and implement methods for process control, process improvement, testing and inspection ... Review customers purchase orders, contracts and change requests and ensure that the necessary ...

Aptiv PLC

Quality Engineer

Warwick, RI · On-site

$90 - $120/hr

Design and implement methods for process control, process improvement, testing and inspection ... Review customers purchase orders, contracts and change requests and ensure that the necessary ...

Ametek

Quality Engineer (Assurance)

Westerly, RI · On-site

$72K - $93K/yr

The Quality Engineer is responsible for ensuring compliance to Level 1 / SUBSAFE and other NAVSEA ... Configuration control and revision integrity * Familiarity with NAVSEA contract requirements and ...

Ametek

Quality Engineer (Assurance)

Westerly, RI

$72K - $93K/yr

The Quality Engineer is responsible for ensuring compliance to Level 1 / SUBSAFE and other NAVSEA ... Configuration control and revision integrity * Familiarity with NAVSEA contract requirements and ...

AMETEK, Inc.

Quality Engineer (Assurance)

Westerly, RI · On-site

$70 - $100/hr

The Quality Engineer is responsible for ensuring compliance to Level 1 / SUBSAFE and other NAVSEA ... Configuration control and revision integrity * Familiarity with NAVSEA contract requirements and ...

Vatn Systems

Quality Engineer

Bristol, RI · On-site

$75K - $97K/yr

Ability to read and interpret engineering drawings, GD&T, and customer/contract specifications ... Familiarity with statistical process control (SPC) Vatn Systems is an equal opportunity employer ...

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Quality Control Contract information

What is a quality control contract?

Quality control contracts are agreements between a company and a service provider or third-party organization to ensure that products or services meet defined quality standards. These contracts outline the specific quality requirements, inspection procedures, and responsibilities of both parties. They are commonly used in manufacturing, construction, and supply chain management to maintain consistency, safety, and compliance with regulatory standards. By using quality control contracts, businesses can minimize defects, avoid costly recalls, and build trust with customers.

What are the key skills and qualifications needed to thrive as a quality control contractor, and why are they important?

To thrive as a Quality Control Contractor, you need a solid understanding of quality assurance methodologies, attention to detail, and typically a background in science, engineering, or a related field. Familiarity with quality management systems (such as ISO 9001), inspection tools, and relevant industry-specific regulations or certifications is often required. Strong analytical skills, effective communication, and problem-solving abilities help professionals stand out in this role. These skills ensure products or services consistently meet standards, minimize defects, and support organizational compliance and customer satisfaction.

What are some typical challenges faced by professionals in quality control contract roles, and how can they be addressed?

Professionals in Quality Control Contract roles often face challenges such as adapting to varying quality standards across different clients, tight project deadlines, and ensuring clear communication with both internal teams and external vendors. To address these challenges, it's important to stay up to date with industry regulations, establish detailed quality checklists, and foster collaborative relationships with all stakeholders. Regular training and open channels of communication can also help ensure that contractual requirements are consistently met while maintaining high-quality outcomes.

What is the difference between Quality Control Contract vs Quality Assurance Technician?

AspectQuality Control ContractQuality Assurance Technician
CertificationsOften requires industry-specific certifications, such as ISO or Six SigmaTypically requires similar certifications, with emphasis on quality standards
Work EnvironmentContract-based, temporary positions in manufacturing, construction, or productionFull-time or temporary roles in manufacturing, laboratories, or production facilities
Employer & Industry UsageUsed by companies seeking temporary quality oversightEmployed by organizations to ensure quality compliance and process improvement

Both roles focus on quality standards, but a Quality Control Contract is usually a temporary, contract-based position, while a Quality Assurance Technician is often a permanent role dedicated to maintaining and improving quality processes within an organization.

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

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

What cities in Rhode Island are hiring for Quality Control Contract jobs?

Cities in Rhode Island with the most Quality Control Contract job openings:

Quality Control Contract jobs near you
Infographic showing various Quality Control Contract job openings in Rhode Island as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution.

QC Informatics Specialist

Pharmaron

Coventry, RI • On-site

$80K - $120K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Job description

Position: Computer System Validation/QC Informatics Specialist
Salary Range: $80,000 - $120,000/yr.
Location: Coventry, RI (On-site)
About Pharmaron
Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.
We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit .
What You'll Do
To support process chemistry and manufacturing activities through management of laboratory data software platforms and workflows. This role is positioned within the Quality Control & Analytical department to develop and support their requirements and workflows and to act as liaison with IT and QA to minimize downtime, improve effectiveness and maintain compliance related to laboratory data generation, storage, and use.
Key Responsibilities
  • With the support of the reporting manager in the Quality Control & Analytical department, lead laboratory improvement efforts related to laboratory information handling such as custom report generation, ELN, LIMS system configuration, data storage/organization, and pharmaceutical data workflows.
  • Liaising with appropriate technical and IT stakeholders to manage GxP software upgrades, installations, and roll outs to ensure business continuity and effectiveness are maintained and improved.
  • Author, review, and perform GxP qualification activities related to QCA as part of the Computer System Validation (CSV) life cycle e.g. GxP Risk & Impact Assessments, URS/FS, Qualification Plan, IQ, OQ, PQ, Requirement Tractability Matrix, Quality Summary Report, periodic reviews and decommissioning activities.
  • Demonstrating expertise in site-wide, complex software platforms e.g. NuGensis LMS, SDMS, ELN, Empower 3 etc. as well as various other standalone laboratory system software used within QCA and Process Chemistry.
  • Support System Owners within business functions with training end users in the use of the system.
  • Liaise between end users and IT to clearly communicate business priorities and ensure that appropriate resources are used to maintain ongoing business operations.
  • Build effective business relationships with all stakeholders.
  • Support departmental or site audits as directed by manager/supervisor as necessary

What We're Looking For
  • MSc or BSc in Chemistry, or Computer Science, or related fields with minimum of 5 years of GxP experience.
  • If qualified in chemistry or a related field, then strong experience in an IT supporting role must be demonstrated including a basic understanding of data structures, programming, and/or information systems.

If qualified in computer science or a related field, then strong experience in an analytical laboratory supporting role must be demonstrated including a basic understanding of common chemistry terminology, application, and laboratory workflows.
  • Direct experience with laboratory informatics (LIMS) systems.
  • Understanding of common GxP topics including QMS, ALCOA+, 21 CFR Part 11, and Data Integrity principles.
  • Evidence of ability to effectively work cross-functionally between IT and scientific teams
  • Working knowledge of applicable FDA, EMA, GAMP, and/or ICH guidance as it relates to data integrity.
  • Evidence of ability to manage stepwise implementation and qualification projects.
  • Good knowledge on pharmaceutical compliance and latest industry requirements.
  • Functional experience in the technical administration of complex laboratory informatics software platforms such as NuGenesis LMS, SDMS and ELN.
  • Effective written and oral communication skills, including the ability to effectively present complex information to colleagues.
  • Effective in managing multiple competing activities and delivering to timelines.
  • Ability to work professionally in a cross-functional environment and clearly reinterpret/translate concepts across IT and Laboratory staff.

Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
  • Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
  • Employee Assistance Program (EAP), mental health resources, and wellness programs
  • Family-friendly benefits, including fertility support and maternity resources
  • Professional development and career growth opportunities within a leading global CRO/CDMO

How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
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