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Quality Control Stability Analyst Jobs in New York

Cellares

Quality Control Analyst

Bridgewater, NJ

$90K - $210K/yr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... reviewing applications, analyzing resumes, or assessing responses and identifying potential ...

Cellares

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... reviewing applications, analyzing resumes, or assessing responses and identifying potential ...

Cellares

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... reviewing applications, analyzing resumes, or assessing responses and identifying potential ...

System One

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model ... Conduct product stability, proficiency, environmental testing, and water system testing * Perform ...

System One

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model ... Conduct product stability, proficiency, environmental testing, and water system testing * Perform ...

System One

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model ... Conduct product stability, proficiency, environmental testing, and water system testing * Perform ...

System One

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model ... Conduct product stability, proficiency, environmental testing, and water system testing * Perform ...

System One

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model ... Conduct product stability, proficiency, environmental testing, and water system testing * Perform ...

System One

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model ... Conduct product stability, proficiency, environmental testing, and water system testing * Perform ...

System One

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model ... Conduct product stability, proficiency, environmental testing, and water system testing * Perform ...

System One

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model ... Conduct product stability, proficiency, environmental testing, and water system testing * Perform ...

System One

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model ... Conduct product stability, proficiency, environmental testing, and water system testing * Perform ...

System One

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model ... Conduct product stability, proficiency, environmental testing, and water system testing * Perform ...

System One

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model ... Conduct product stability, proficiency, environmental testing, and water system testing * Perform ...

PSG Global Solutions

Quality Control Analyst

Summit, NJ · On-site

$25.50 - $34.25/hr

May conduct routine release and stability analyses of developmental compounds, prototype formulations and finished products in support of clinical testing for IND and NDA submissions. * Perform ...

BERJE INCORPORATED

QC Analyst

Carteret, NJ

$26 - $31/hr

Reporting to the Quality Control leadership team, the Quality Control Analyst is responsible for performing analytical testing of raw materials, intermediates, and finished products to ensure ...

Kashiv Biosciences LLC

QC Analyst III

Piscataway, NJ · On-site

$103K/yr

Job Type Full-time Description QC Analyst III (Piscataway, NJ): Be primarily responsible for the ... assays for release & stability purposes in a GMP-complaint Quality Control laboratory ...

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All JobsQuality Control Stability Analyst JobsQuality Control Stability Analyst Jobs in New York

Quality Control Stability Analyst information

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 are popular job titles related to Quality Control Stability Analyst jobs in New York?

For Quality Control Stability Analyst jobs in New York, the most frequently searched job titles are:

What job categories do people searching Quality Control Stability Analyst jobs in New York look for?

The top searched job categories for Quality Control Stability Analyst jobs in New York are:

What cities in New York are hiring for Quality Control Stability Analyst jobs?

Cities in New York with the most Quality Control Stability Analyst job openings:

Quality Control Stability Analyst jobs near you

QUALITY CONTROL CHEMIST I

ASPIRE PHARMACEUTICALS INC

Somerset, NJ

Other

Re-posted 8 days ago

Job description

Position Description: Position Summary:The Quality Control Chemist-I is responsible for conducting routine testing and analysis of raw materials, in-process materials, and finished product samples using various analytical methodologies to ensure the quality of dietary supplements and OTC products. This role includes reviewing and maintaining Standard Operating Procedures (SOPs), Testing Procedures, calibrations, and other controlled documents to ensure compliance with regulatory standards and internal procedures. Additionally, the Chemist-I will assist in quality control stability testing and contribute to maintaining accurate records and documentation.DUTIES AND RESPONSIBILITIES:Ensure all work is performed in compliance with cGMP, GLP, compendia standards, and internal procedures. Conduct wet chemistry and analytical testing on raw materials, finished products, in-process samples, stability, and packaged products according to Testing Procedures.Assist in quality control stability testing, prepare, and maintain stability records and summaries.Operate, maintain, and troubleshoot analytical instruments, including pH meter, FTIR, TOC, UV, and others as necessary.Maintain accurate records of all analyses, ensuring contemporaneous documentation and adherence to company standards.Perform laboratory analysis right the first time and ensure all results are properly documented.Conduct laboratory investigations under the guidance of laboratory management.Work effectively under the direction of supervisors and/or manager, and perform additional duties as required.QUALIFICATION AND EXPERIENCE:Bachelor’s degree in chemistry, Biochemistry, Pharmaceutical Sciences, or related field with 0 - 3 years of relevant experience in a quality control setting; or an equivalent combination of education and experience.Basic understanding of Current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and quality control principles in the pharmaceutical industry.Math skills commensurate with a scientific background are required.Ability to communicate test results and observations clearly, both verbally and in writing. Ability to follow written instructions and solve basic analytical problems using standard procedures.

Aspire Pharmaceuticals logo

About Aspire Pharmaceuticals

Sourced by ZipRecruiter

Aspire Pharmaceuticals was established more than a decade ago with the sole purpose of bringing innovation and excellence to the encapsulation category. Billions of softgel later, the business has grown exponentially with a customer roster that represents some of the most influential players in the nutritional supplement and OTC industries. Aspire’s passion in the encapsulation space has moved beyond softgel to include liquid capsules and liposome technology, all of which allow us to offer a larger variety of solutions to customers. As a leader in the development AND manufacturing of softgel and liquid capsule supplements and OTC products, we take that role with pride. Our promise to you is that we will never stop asking the question: How can we do it better? We’ve been asking that very same question each year since our inception.

Industry

Pharmaceutical and medicine manufacturing

Company size

51 - 200 Employees

Headquarters location

Somerset, NJ, US

Year founded

2009

Social media

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