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Quality Control Stability Jobs in Rhode Island (NOW HIRING)

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 ...

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 ...

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

Create Quality Control Plans (QCPs) in advance of first-time builds and new production runs ... The environment encourages collaboration, stability, and long-term growth, offering a workplace ...

Quality Lab Technician

North Kingstown, RI

$19.25 - $24.25/hr

The Quality Lab Technician will provide support for the Quality Control technicians by performing ... Prepare and perform stability study testing of finished products * Identify and isolate finished ...

As a Quality Control Inspector , you are the final line of defense in ensuring our precision metal ... Competitive Stability: Join a forward-thinking manufacturing team that offers a clear compensation ...

... 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 ...

Backed by 45+ years of success, Uline offers opportunities to grow your career with stability you ... Serve as the go-to resource for product changes, quality concerns and inventory questions between ...

Quality Manager

East Providence, RI · On-site

$130K - $150K/yr

... stability. Reporting to the Sr. Director Operations & Quality Director, this role will be ... Maintain PFMEA, Control Plan, inspection standards and quality gates as living documents aligned ...

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Quality Control Stability information

What career paths are possible in QC?

Career paths in Quality Control (QC) include roles such as QC Technician, QC Analyst, Quality Assurance Specialist, and Quality Manager. Advancement often involves gaining experience, certifications like ASQ certifications, and developing skills in inspection, testing, and data analysis within manufacturing, pharmaceuticals, or food industries.

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.

Which pays more, QA or QC?

In the field of Quality Control Stability, Quality Assurance (QA) roles generally offer higher salaries than Quality Control (QC) positions due to their broader responsibilities and focus on process improvement. QA jobs often require more experience and may involve certifications like Six Sigma or ISO standards, which can also influence pay. However, salaries vary based on industry, location, and level of experience.

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 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.

Is QC analyst a stressful job?

A QC analyst role involves inspecting and testing products to ensure quality standards are met, which can be demanding during tight deadlines or when addressing product issues. The job often requires attention to detail, adherence to safety protocols, and sometimes working in environments with strict regulatory requirements, which can contribute to stress levels.

What is quality control salary?

The salary for a quality control stability role typically ranges from $40,000 to $70,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced professionals with certifications can earn higher wages. Salaries often include benefits such as health insurance and paid time off.
What are popular job titles related to Quality Control Stability jobs in Rhode Island? For Quality Control Stability jobs in Rhode Island, the most frequently searched job titles are:
What job categories do people searching Quality Control Stability jobs in Rhode Island look for? The top searched job categories for Quality Control Stability jobs in Rhode Island are:
What cities in Rhode Island are hiring for Quality Control Stability jobs? Cities in Rhode Island with the most Quality Control Stability job openings:

Quality Control Associate - Bioanalytics

ApTask Global Workforce

West Greenwich, RI • On-site

$24.41/hr

Other

Medical, Dental, Vision, Life

Posted yesterday


Job description

Aptask Global Workforce (AGW) is seeking a Quality Control Associate - Bioanalytics for an Onsite position with a Global Biotechnology Company located in West Greenwich, RI. This is a 12+ month contract opportunity.
This role will be based on-site and will work under the mentorship of the front-line manager. The Bioanalytics team provides analytical expertise in testing in-process, release and stability samples. The laboratory employs a variety of test methodologies that use sophisticated equipment including: HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as: Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing.
Responsibilities:
  • Follow safety guidelines, cGMPs (Good Manufacturing Practices) and other applicable regulatory requirements
  • Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks
  • Ensure that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations
  • Operate laboratory equipment and instrumentation
  • Perform review and approval of assays, documents and records
  • Support Continual Improvement initiatives
  • Alert management of quality, compliance, supply and safety risks
  • Participate in laboratory investigations
  • Perform general laboratory housekeeping activities
  • Complete required assigned training to permit carry through of required tasks
  • Perform additional duties as specified by management

Requirements:
  • High school diploma/GED and 2 years of work experience OR
  • Associate's degree and 6 months of work experience OR
  • Bachelor's degree

Desired skills:
  • 1-2 years experience in HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as: Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing
  • Demonstrated experience in laboratory investigations, method validation, audits, QC processes
  • Proven ability to interpret scientific data
  • Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal direction

Pay range: up to $24.41 per hour
Only candidates available and ready to work directly as Aptask Global Workforce (AGW) employees will be considered for this position.
If you have the described qualifications and are interested in this exciting opportunity, apply today!
Aptask Global Workforce (AGW)
ApTask Global Workforce (AGW) is a certified Minority and Veteran workforce solutions company. AGW delivers operational, clinical, lab and professional talent with a strong focus on healthcare and life sciences. The company supports clients with reliable staffing, program expertise and a commitment to quality, speed and consistent delivery.
Benefits of working with ApTask Global Workforce include:
  • Medical
  • Dental
  • Vision
  • Sick Pay (for applicable states/municipalities)

Our team stays close to the process and is here to guide you every step of the way. To learn more, please visit our website
ApTask Global Workforce is an Equal Opportunity Employer. Candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran.