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Quality Control Stability Jobs in Warwick, RI (NOW HIRING)

Amgen, Inc.

QC Specialist

West Greenwich, RI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

QC Specialist What you will do Let's do this. Let's change the world. In this vital role you will ... testing, stability, environmental monitoring, cleaning validation, and finished product testing.

Amgen

QC Specialist

West Greenwich, RI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

QC Specialist What you will do Let's do this. Let's change the world. In this vital role you will ... testing, stability, environmental monitoring, cleaning validation, and finished product testing.

RD Partners

Quality Control Analyst I

Norton, MA · On-site

$50K - $63K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

R&D Partners is seeking to hire a Quality Control Analyst I in Norton, MA. Your main ... stability studies under supervision, following established SOPs * Maintain up-to-date training ...

Cipla

QC Sampling Associate

Fall River, MA · On-site

$25 - $29/hr

Conduct sample loading in stability chambers and submitting stability samples as per schedule. * Provide general housekeeping in the QC lab and any other functional activity as assigned by management.

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Quality Control Analyst I (cur_1_129008@curatelyai.net)

Norton, MA · On-site

$31/hr

  • Dental

Quality Control Analyst I Location: Norton, MA 02766 Duration: 12 Months Pay rate: $31/hr. on w2 ... stability studies under supervision, following established SOPs * Maintain up-to-date training ...

New

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Analyst IV, Quality Control Technical (cur_1_129153@curatelyai.net)

Norton, MA · On-site

$50 - $70/hr

  • Dental

The Quality Control Technical Services (QCTS) Analyst IV plays a crucial role in supporting the ... In addition to active participation in stability studies, data trending, and investigations, this ...

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CARLISLE COMPANIES

Quality Technician

East Providence, RI · On-site

$25.87/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... stability, agility, and opportunity in a performance-driven culture. Do meaningful work and shape ... We are seeking a QC Tech in our East Providence, RI Plant. Shift: 6am-3pm, OT as required Pay: $25 ...

Carlisle Companies, Inc.

Quality Technician

Providence, RI · On-site

$25.87/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... stability, agility, and opportunity in a performance-driven culture. Do meaningful work and shape ... We are seeking a QC Tech in our East Providence, RI Plant. Shift: 6am-3pm, OT as required Pay: $25 ...

Carlisle Companies, Inc.

Quality Technician

Providence, RI · On-site

$25.87/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... stability, agility, and opportunity in a performance-driven culture. Do meaningful work and shape ... We are seeking a QC Tech in our East Providence, RI Plant. Shift: 6am-3pm, OT as required Pay: $25 ...

Carlisle Companies, Inc.

Quality Technician

Providence, RI · On-site

$25.87/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... stability, agility, and opportunity in a performance-driven culture. Do meaningful work and shape ... We are seeking a QC Tech in our East Providence, RI Plant. Shift: 6am-3pm, OT as required Pay: $25 ...

Metals USA

Quality Manager

Seekonk, MA

Executes and implements the administration of quality assurance control policies and practices in ... stability studies, corrective actions and re-validations. * Adheres to the Reliance's Code of ...

Metals USA

Quality Manager

Seekonk, MA · On-site

Executes and implements the administration of quality assurance control policies and practices in ... stability studies, corrective actions and re-validations. * Adheres to the Reliance's Code of ...

Metals USA

Quality Manager

Seekonk, MA · On-site

Executes and implements the administration of quality assurance control policies and practices in ... stability studies, corrective actions and re-validations. * Adheres to the Reliance's Code of ...

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Showing results 1-20

All JobsQuality Control Stability JobsQuality Control Stability Jobs in Warwick, RI

Quality Control Stability information

See Warwick, RI salary details

$30.6K

$81.5K

$129.9K

How much do quality control stability jobs pay per year?

As of Aug 20, 2026, the average yearly pay for quality control stability in Warwick, RI is $81,545.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,700.00 and $100,300.00 per year, depending on experience, location, and employer.

What is a quality control stability role?

A Quality Control Stability role involves monitoring and evaluating the stability of pharmaceutical products, ensuring they maintain their quality, safety, and efficacy throughout their shelf life. Professionals in this position design and execute stability studies, analyze the results, and document findings according to regulatory requirements. They play a crucial part in ensuring compliance with industry standards and supporting product development and release. This role typically requires expertise in analytical testing, regulatory guidelines, and laboratory practices.

What are some common challenges faced in a quality control stability role, and how can they be addressed?

Professionals in Quality Control Stability often encounter challenges such as managing tight timelines for stability testing, interpreting ambiguous results, and ensuring compliance with evolving regulatory requirements. Effective communication with cross-functional teams—such as R&D, production, and regulatory affairs—is essential to address discrepancies and maintain data integrity. Staying organized, maintaining thorough documentation, and keeping up to date with industry guidelines help mitigate these challenges and ensure smooth workflow.

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

To thrive as a Quality Control Stability specialist, you need a solid background in chemistry or related sciences, experience with stability testing, and typically a bachelor’s degree in a scientific field. Familiarity with laboratory instruments (such as HPLC, GC), stability management systems, and knowledge of regulatory guidelines like ICH are essential. Attention to detail, problem-solving, and strong organizational skills help ensure accurate data analysis and effective reporting. These abilities are crucial for maintaining compliance, product safety, and reliability in pharmaceutical or biotech environments.

What is the difference between Quality Control Stability vs Quality Control Inspector?

AspectQuality Control StabilityQuality Control Inspector
CertificationsOften requires certifications like Six Sigma, ISO auditor, or quality management certificationsTypically requires quality inspection certifications or training
Work EnvironmentFocuses on maintaining process stability in manufacturing or production settingsPerforms inspections on products or materials on the production line
Employer & Industry UsageUsed in manufacturing, aerospace, automotive, and industries emphasizing process consistencyCommon in manufacturing, food production, and assembly lines

Quality Control Stability involves ensuring that manufacturing processes remain consistent over time, emphasizing process control and reduction of variability. In contrast, a Quality Control Inspector primarily conducts inspections to verify product quality at various stages. Both roles are essential in quality management but focus on different aspects of quality assurance.

Is quality control stability a good career choice?

Quality Control Stability is a role focused on maintaining product consistency and compliance through testing and monitoring processes. It often requires attention to detail, knowledge of industry standards, and proficiency with testing tools or software. This career can offer steady employment opportunities in manufacturing, pharmaceuticals, or food industries, with potential for advancement and certification.

Is quality control stability a good career path?

Quality control stability involves ensuring products meet quality standards over time, often requiring attention to detail and knowledge of testing procedures. It can offer steady employment and opportunities for advancement in manufacturing, pharmaceuticals, or food industries, especially for those with relevant certifications or experience. The career can be stable, but growth depends on industry demand and individual skill development.

What job categories do people searching Quality Control Stability jobs in Warwick, RI look for?

The top searched job categories for Quality Control Stability jobs in Warwick, RI are:

Quality Control Stability jobs near you
Infographic showing various Quality Control Stability job openings in Warwick, RI as of August 2026, with employment types broken down into 75% Full Time, and 25% Part Time. Highlights an 100% In-person job distribution, with an average salary of $81,545 per year, or $39.2 per hour.

Quality Control Chemist

Integrated Resources, Inc

Norton, MA

$25 - $30/hr

Full-time

Posted 6 days ago

Job description

Title: Quality Control Chemist
Location: Norton, MA
Duration: 12 months+
Pay Range: $25 - $30/hr. on w2
Overview
The Analyst I in Quality Control Operations will play a critical role in executing assays, generating accurate and reliable data, and supporting the general operations of the laboratory to ensure the quality and compliance of our products from development through to commercialization .
This position is onsite and will be primarily located in Norton, MA. There may occasional responsibilities at a secondary location in Cambridge, MA.
Key Responsibilities (including but not limited to):
  • Perform routine and non-routine analytical assays to support raw materials, in-process samples, product release, and stability studies under supervision, following established SOPs
  • Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities and uphold the department's commitment to meeting project timelines and quality metrics
  • Assist in the maintenance of laboratory equipment and inventory, including the preparation of reagents and samples to ensure smooth laboratory operations
  • Accurately record experimental data and observations in compliance with GxP standards. Participate in the review of data commensurate with experience.
  • Contribute to the revision and updating of controlled documents, including SOPs, work instructions, and test methods, to ensure continuous improvement and compliance with current industry standards and regulatory requirements
  • Adhere to internal standards, policies, and SOPs, as well as regulatory and industry standards (e.g., GMP, GLP, ICH guidelines) to maintain the highest levels of quality and compliance.
  • Actively participate in continuous improvement efforts by identifying and suggesting enhancements to methods and laboratory processes, particularly those related to efficiency and reliability.
  • Collaborate with QC and cross-functional teams to ensure seamless quality control operations and to support the collective Client goals
  • Pursue ongoing training and development to deepen expertise in QC analytical techniques and regulatory compliance.
Qualifications
  • Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.
  • 0 to 2 years of experience in a GMP/GLP regulated laboratory environment, with exposure to pharmaceutical or biotechnology industries preferred.
  • Understanding of analytical techniques and their application in raw materials, in-process testing, release, and stability studies is preferred.
  • Strong documentation skills and attention to detail, with an unwavering commitment to quality and compliance.
  • Basic awareness of regulatory guidelines relevant to pharmaceutical QC (GMP, GLP, ICH) is desirable.
  • Effective communication and teamwork skills, with the ability to work collaboratively across functions.
  • Capable of working under supervision and following detailed instructions.
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Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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