1

Quality Control Stability Analyst Jobs in Warwick, RI

Gas Quality Control Analyst

New Bedford, MA ยท On-site

$24.25 - $32.50/hr

The QC Specialist has the authority to direct and stop, if necessary, work to ensure compliance ... Mental Aspects : * Work includes analyzing, planning, organizing, evaluating and documenting.

Gas Quality Control Analyst

Taunton, MA ยท On-site

$24.50 - $33/hr

The QC Specialist has the authority to direct and stop, if necessary, work to ensure compliance ... Mental Aspects : * Work includes analyzing, planning, organizing, evaluating and documenting.

Gas Quality Control Analyst

New Bedford, MA ยท On-site

$24.25 - $32.50/hr

The QC Specialist has the authority to direct and stop, if necessary, work to ensure compliance ... Mental Aspects : * Work includes analyzing, planning, organizing, evaluating and documenting.

Quality Control (QC) Chemist

Fall River, MA ยท On-site

$65K - $105K/yr

What You'll Do Analytical Testing & Expertise * Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) * Evaluate ...

Quality Control (QC) Chemist

Fall River, MA ยท On-site

$65K - $105K/yr

What You'll Do Analytical Testing & Expertise * Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) * Evaluate ...

Quality Control

Fall River, MA ยท On-site

$27.05/hr

Uses analytical and statistical data to project product quality and reliability. * Gives technical ... Writes and distributes quality control reports and educational material, utilizing internal systems ...

Uses analytical and statistical data to project product quality and reliability. * Gives technical ... Writes and distributes quality control reports and educational material, utilizing internal systems ...

Uses analytical and statistical data to project product quality and reliability. * Gives technical ... Writes and distributes quality control reports and educational material, utilizing internal systems ...

Quality Control

Fall River, MA ยท On-site

$27.05/hr

Uses analytical and statistical data to project product quality and reliability. * Gives technical ... Writes and distributes quality control reports and educational material, utilizing internal systems ...

Analytical Investigation Ownership * Lead Quality Control analytical investigations for Out-of-Specification (OOS), Out-of-Trend (OOT), atypical, and unexpected analytical results. * Perform ...

Analytical Investigation Ownership * Lead Quality Control analytical investigations for Out-of-Specification (OOS), Out-of-Trend (OOT), atypical, and unexpected analytical results. * Perform ...

Specialist QC

West Greenwich, RI ยท On-site

$95 - $125/hr

Analytical Investigation Ownership * Lead Quality Control analytical investigations for Out-of-Specification (OOS), Out-of-Trend (OOT), atypical, and unexpected analytical results. * Perform ...

next page

Showing results 1-20

Quality Control Stability Analyst information

See Warwick, RI salary details

$16

$27

$41

How much do quality control stability analyst jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for quality control stability analyst in Warwick, RI is $27.99, according to ZipRecruiter salary data. Most workers in this role earn between $23.12 and $31.11 per hour, depending on experience, location, and employer.

What is a quality control stability analyst?

Quality Control Stability Analysts are professionals responsible for testing and evaluating the stability of pharmaceutical products over time. They design, conduct, and interpret experiments to ensure products maintain their safety, potency, and quality throughout their shelf life. Their work is crucial for regulatory compliance, as they document and report stability data according to industry standards and guidelines. These analysts often work in laboratory environments and collaborate closely with quality assurance and manufacturing teams.

What are the key skills and qualifications needed to thrive as a quality control stability analyst?

To thrive as a Quality Control Stability Analyst, you need a solid background in chemistry or related sciences, familiarity with Good Laboratory Practices (GLP), and often a relevant bachelor's degree. Experience with laboratory instrumentation such as HPLC, GC, and LIMS, along with knowledge of regulatory guidelines like ICH and FDA, is typically required. Attention to detail, strong organizational skills, and effective communication are critical soft skills in this role. These competencies ensure accurate data analysis, compliance with regulations, and reliable stability testing to maintain product quality and safety.

What are some typical challenges faced by quality control stability analysts, and how can they be addressed?

Quality Control Stability Analysts often face challenges such as managing multiple projects with tight timelines, accurately interpreting stability data, and ensuring compliance with stringent regulatory requirements. Balancing the need for meticulous documentation with the fast-paced nature of product development can also be demanding. To address these challenges, analysts benefit from strong organizational skills, effective communication with cross-functional teams (like R&D and production), and ongoing training on evolving industry standards and regulatory guidelines.

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

AspectQuality Control Stability AnalystQuality Control Analyst
CertificationsGMP, GLP, relevant laboratory certificationsGMP, GLP, relevant laboratory certifications
Work EnvironmentPharmaceutical, biotech labs focusing on stability testingManufacturing labs, quality testing environments
Job FocusMonitoring product stability over time, data analysis for stability programsPerforming routine quality tests, raw material and finished product testing

The main difference is that a Quality Control Stability Analyst specializes in stability testing and data analysis related to product shelf life, while a Quality Control Analyst performs general quality testing. Both roles require similar certifications and work in related environments, but their focus areas differ within the quality assurance process.

How much does a quality control stability analyst earn?

A quality control stability analyst typically earns between $50,000 and $80,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced analysts with certifications can earn higher salaries. The role often requires knowledge of stability testing, laboratory skills, and regulatory standards.

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

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

What cities near Warwick, RI are hiring for Quality Control Stability Analyst jobs?

Cities near Warwick, RI with the most Quality Control Stability Analyst job openings:

Tech Ops and Quality - Quality Control Analyst I

TalentBurst, Inc.

Norton, MA โ€ข On-site

$24.25 - $32.75/hr

Full-time

Medical, Dental, Vision, Retirement

Posted 11 days ago


Job description

Title: Quality Control Operations Analyst I
Duration: 12 months
Location: Norton MA
  • This position is onsite and will be primarily located in Norton, MA.
  • There may occasional responsibilities at a secondary location in Cambridge,MA.

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.

Key Responsibilities:
  • 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 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
#TB_PH
#ZR
#Linkd

Why TalentBurst?
At TalentBurst, we deliver more than talent, we deliver outcomes. We partner with you to move quickly and connect you to opportunities aligned with your skills and long term growth.

Backed by precision, transparency, and results, we connect top talent with leading organizations through trusted partnerships.

We offer competitive compensation and comprehensive benefits, including medical, dental, vision, and retirement options.

TalentBurst is an equal opportunity employer committed to an inclusive and diverse workforce.

Company Description

Founded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website www.talentburst.com or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX & downtown San Francisco, CA


TalentBurst logo

About TalentBurst

Sourced by ZipRecruiter

TalentBurst is a leading provider of Information Technology and Engineering staffing solutions based in Natick, Massachusetts, US. An industry veteran with two decades of experience in their portfolio, the company's services range from IT consulting, life sciences, HR solutions, payroll services, and more. TalentBurst was founded with a mission to provide world-class, global staffing services to clients of all sizes. They strive to provide unmatched quality and service to their clients, which has earned them the reputation of being a highly respected and trusted staffing firm.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Natick, MA, US

Year founded

2002

Social media