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Quality Control Manager Jobs in Rhode Island (NOW HIRING)

Pharmaron

Senior Scientist I, QC

Coventry, RI · On-site

$100K - $140K/yr

Manage stability studies, draft stability protocols and report, coordinate and perform sample ... Ensure high quality in QC work and accurately document all necessary and relevant information in a ...

Pharmaron

Senior Scientist I, QC

Coventry, RI · On-site

$100K - $130K/yr

Manage stability studies, draft stability protocols and report, coordinate and perform sample ... Ensure high quality in QC work and accurately document all necessary and relevant information in a ...

MasTec Industrial

Quality Inspector, (CWI)

Cranston, RI · On-site

$35.64 - $55.30/hr

The Quality Inspector will report directly to the site Quality Manager, with indirect oversight ... Conduct regularly scheduled QA/QC meetings, review logs of Deficiencies, Punch List, and other ...

MasTec Industrial

Quality Inspector, (CWI)

Providence, RI · On-site

$35.64 - $55.30/hr

The Quality Inspector will report directly to the site Quality Manager, with indirect oversight ... Conduct regularly scheduled QA/QC meetings, review logs of Deficiencies, Punch List, and other ...

MasTec Industrial

Quality Inspector, (CWI)

Warwick, RI · On-site

$35.64 - $55.30/hr

The Quality Inspector will report directly to the site Quality Manager, with indirect oversight ... Conduct regularly scheduled QA/QC meetings, review logs of Deficiencies, Punch List, and other ...

Pharmaron

Senior Scientist I, QC (3rd shift)

Coventry, RI · On-site

$100K - $140K/yr

... management in compliance with all applicable guidelines. Will also solve moderate complexity ... Mentor junior QC scientists on daily work, provide technical and compliance guidance. * Conduct ...

Pharmaron

Senior Scientist I, QC (3rd shift)

Coventry, RI · On-site

$100K - $140K/yr

... management in compliance with all applicable guidelines. Will also solve moderate complexity ... Mentor junior QC scientists on daily work, provide technical and compliance guidance. * Conduct ...

Aptiv

Quality Inspection Supervisor

Warwick, RI · On-site

This role involves managing a team of quality control inspectors, documenting inspection outcomes, creating Quality Alerts and sorting instructions, and training to inspection instructions. The ...

Aptiv PLC

Quality Inspection Supervisor

Warwick, RI · On-site

This role involves managing a team of quality control inspectors, documenting inspection outcomes, creating Quality Alerts and sorting instructions, and training to inspection instructions. The ...

Aptiv

Quality Inspection Supervisor

Warwick, RI

This role involves managing a team of quality control inspectors, documenting inspection outcomes, creating Quality Alerts and sorting instructions, and training to inspection instructions. The ...

SAIC

Quality Assurance Supervisor

Middletown, RI · On-site

This role involves managing the ISO 9001 quality control processes, coordinating inspections, providing leadership for compliance initiatives, and driving consistent quality improvement. The ideal ...

New

Aptiv PLC

Quality Inspection Supervisor

Warwick, RI · On-site

This role involves managing a team of quality control inspectors, documenting inspection outcomes, creating Quality Alerts and sorting instructions, and training to inspection instructions. The ...

Aptiv PLC

Quality Inspection Supervisor

Warwick, RI

This role involves managing a team of quality control inspectors, documenting inspection outcomes, creating Quality Alerts and sorting instructions, and training to inspection instructions. The ...

SAIC

Quality Assurance Supervisor

Middletown, RI

This role involves managing the ISO 9001 quality control processes, coordinating inspections, providing leadership for compliance initiatives, and driving consistent quality improvement. The ideal ...

New

SAIC

Quality Assurance Supervisor

Middletown, RI

This role involves managing the ISO 9001 quality control processes, coordinating inspections, providing leadership for compliance initiatives, and driving consistent quality improvement. The ideal ...

New

SAIC

Quality Assurance Supervisor

Middletown, RI · On-site

This role involves managing the ISO 9001 quality control processes, coordinating inspections, providing leadership for compliance initiatives, and driving consistent quality improvement. The ideal ...

New

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Showing results 41-60

All JobsQuality Control JobsQuality Control Manager JobsQuality Control Manager Jobs in Rhode Island

Quality Control Manager information

See Rhode Island salary details

$29.9K

$79.6K

$126.8K

How much do quality control manager jobs pay per year?

As of Aug 10, 2026, the average yearly pay for quality control manager in Rhode Island is $79,641.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,200.00 and $97,900.00 per year, depending on experience, location, and employer.

What does a quality control manager do?

A Quality Control Manager is responsible for overseeing and ensuring the quality of products or services within an organization. They develop and implement quality control procedures, inspect products, and monitor operations to ensure compliance with industry standards and regulations. Additionally, they analyze quality data, identify areas for improvement, and work closely with other departments to resolve quality issues. Their goal is to maintain high standards and minimize defects or errors in the final output.

What is the difference between Quality Control Manager vs Quality Assurance Supervisor?

AspectQuality Control ManagerQuality Assurance Supervisor
Primary FocusInspecting products and processes to identify defectsDeveloping and implementing quality systems and procedures
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, production lines, labsQuality departments, process improvement teams
Employer UsageManufacturers, factories, production facilitiesCompanies with formal quality management systems

Both roles focus on quality but differ in scope. The Quality Control Manager primarily inspects products to catch defects, while the Quality Assurance Supervisor develops systems to prevent defects. Understanding these differences helps in choosing the right career path or hiring focus.

What are the biggest challenges a quality control manager typically faces when implementing new quality standards?

One of the main challenges Quality Control Managers encounter is ensuring that all team members understand and consistently adhere to newly implemented quality standards. This often involves extensive training, clear documentation, and continuous monitoring to address resistance to change or misunderstandings. Additionally, balancing the need for thorough quality checks with production deadlines can be demanding, requiring strong communication and problem-solving skills to align quality goals with operational efficiency. Collaborative efforts with production, engineering, and compliance teams are essential to successfully integrate new standards while maintaining workflow.

What does a quality control manager do?

As a quality control manager, your responsibilities are to ensure that your company’s products are up to industry standards by inspecting items and overseeing the efficiency of production and manufacturing processes. Your job duties as a quality control manager include coordinating between company management and production departments, implementing strategies to maximize employee efforts, and evaluating processes on manufacturing and production lines. Your focus is on quality assurance of both processes and output to minimize the number of problems that inspectors might identify when visiting the company.

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

To thrive as a Quality Control Manager, you need expertise in quality assurance processes, analytical skills, and a background in science or engineering, often supported by a relevant degree. Familiarity with quality management systems (such as ISO 9001), statistical analysis software, and internal auditing tools is typically required. Strong leadership, problem-solving abilities, and excellent communication help drive team performance and foster a culture of continuous improvement. These skills ensure that products meet strict standards, reduce defects, and maintain customer satisfaction in a competitive market.
More about Quality Control Manager jobs
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 are popular job titles related to Quality Control Manager jobs in Rhode Island? For Quality Control Manager jobs in Rhode Island, the most frequently searched job titles are:
What job categories do people searching Quality Control Manager jobs in Rhode Island look for? The top searched job categories for Quality Control Manager jobs in Rhode Island are:
What cities in Rhode Island are hiring for Quality Control Manager jobs? Cities in Rhode Island with the most Quality Control Manager job openings:
What are popular job titles related to Quality Control Manager jobs in RI? For Quality Control Manager jobs in RI, the most frequently searched job titles are:
Quality Control Manager jobs near you
Infographic showing various Quality Control Manager job openings in Rhode Island as of August 2026, with employment types broken down into 82% Full Time, 9% Part Time, and 9% Contract. Highlights an 100% In-person job distribution, with an average salary of $79,641 per year, or $38.3 per hour.

Senior Scientist I, QC

Pharmaron

Coventry, RI • On-site

$100K - $140K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 29 days ago

Job description

Position: Senior Scientist I, QC
Salary Range: $100,000-$130,000
Location: Coventry, RI
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 .
Job Overview:
The Senior Scientist, QC supports technology transfer and GMP manufacturing activities through analytical method transfer, verification, validation, sample testing and stability study management in compliance with all applicable guidelines. Will also solve moderate complexity analytical and quality control issues for assigned projects and/or initiatives.
Key Responsibilities
  • Participate in method transfer activities, including writing method transfer and method validation protocols, executing experiments and writing reports.
  • Mentor junior QC scientists on daily work, provide technical and compliance guidance.
  • Conduct method validation, method verification and sample testing.
  • Review experimental data, notebooks, method, protocols / reports.
  • Manage stability studies, draft stability protocols and report, coordinate and perform sample testing.
  • Actively participate in investigation of laboratory deviations, OOS, OOT, and atypical results. Write investigation reports.
  • Prepare and present data summaries (written and oral) as necessary. Present to cross functional teams and effectively communicate critical QC/analytical issues and solutions.
  • Ability to work successfully in both a team/matrix environment as well as independently.
  • Ensure high quality in QC work and accurately document all necessary and relevant information in a clear concise manner as per cGMPs.
  • Participate, support and facilitate site audits as directed and required.
  • SME for instrument and training.
  • Maintain good laboratory practices and GMP in compliance with safety and environmental requirements.
  • Write, revise, develop, and evaluate SOPs.
  • Perform other related assignments and duties, as required and assigned.

What We're Looking For
  • MS with 8+ years of experience or BS with 10 years of experience in pharmaceutical industry
  • Evidence of experience in successful application of analytical skill sets to resolve scientific problems related to method optimization and/or implementation.
  • Experienced troubleshooter of technical problems
  • 3 years of experience (may include Ph.D. experience) with core analytical instrumentation such as HPLC, GC, FTIR, Mass Spectrometry.
  • Evidence of ability to effectively contribute to multi-disciplinary scientific teams
  • Working knowledge of cGLP/cGMP and applicable FDA, EMA and ICH guidance
  • Evidence of ability to effectively scientifically supervise staff
  • Expert application of core laboratory techniques and instrumentation to impact API, intermediates and starting materials

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 21,000 employees and operations in the U.S., the U.K. and China. 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:
  • Insurance including Medical, Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program

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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