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Qc Stability Jobs in Edison, NJ (NOW HIRING)

Novartis

Senior Expert Stability

East Hanover, NJ · On-site

$118K/yr

Data management to support the Stability Programs including the administration and distribution of Quality Control (QC) stability samples, associated document coordination, and collection and ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and Manufacturing to meet production timelines Requirements * 6-8+ years of pharmaceutical QC experience (cGMP ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and Manufacturing to meet production timelines Requirements * 6-8+ years of pharmaceutical QC experience (cGMP ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and Manufacturing to meet production timelines Requirements * 6-8+ years of pharmaceutical QC experience (cGMP ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and Manufacturing to meet production timelines Requirements * 6-8+ years of pharmaceutical QC experience (cGMP ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and Manufacturing to meet production timelines Requirements * 6-8+ years of pharmaceutical QC experience (cGMP ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and Manufacturing to meet production timelines Requirements * 6-8+ years of pharmaceutical QC experience (cGMP ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and Manufacturing to meet production timelines Requirements * 6-8+ years of pharmaceutical QC experience (cGMP ...

WuXi Biologics

Scientist I, QC

Cranbury, NJ · On-site

$60K - $96K/yr

Supports the QC Operations group in RS/Stability/inventory management. Essential Job Functions * Lead multiple matrix teams involving Analytical development, QC testing teams to establish and ...

WuXi Biologics

Scientist I, QC

Cranbury, NJ · On-site

$60K - $96K/yr

Supports the QC Operations group in RS/Stability/inventory management. Essential Job Functions * Lead multiple matrix teams involving Analytical development, QC testing teams to establish and ...

Cellares

Manager, Quality Control

Bridgewater, NJ

$90K - $210K/yr

Create/Review and approve stability protocols and reports * Create/Review and approve quality control operation procedures * Manage the validation of analytical methods used in QC as well as the ...

Cellares

Manager, Quality Control

Bridgewater, NJ · On-site

$90K - $210K/yr

Create/Review and approve stability protocols and reports * Create/Review and approve quality control operation procedures * Manage the validation of analytical methods used in QC as well as the ...

Cellares

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... Operating Procedures * Supply Quality Control data necessary for regulatory submissions * Support ...

Cellares

Quality Control Analyst

Bridgewater, NJ

$90K - $210K/yr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... Operating Procedures * Supply Quality Control data necessary for regulatory submissions * Support ...

Cellares

Manager, Quality Control

Bridgewater, NJ · On-site

$90K - $210K/yr

Create/Review and approve stability protocols and reports * Create/Review and approve quality control operation procedures * Manage the validation of analytical methods used in QC as well as the ...

Cellares

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... Operating Procedures * Supply Quality Control data necessary for regulatory submissions * Support ...

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All JobsQc Stability JobsQc Stability Jobs in Edison, NJ

Qc Stability information

See Edison, NJ salary details

$31.6K

$84.2K

$134.1K

How much do qc stability jobs pay per year?

As of Aug 21, 2026, the average yearly pay for qc stability in Edison, NJ is $84,190.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,600.00 and $103,500.00 per year, depending on experience, location, and employer.

What is a QC Stability?

A QC Stability job focuses on monitoring and evaluating the stability of pharmaceutical products over time to ensure they maintain their quality, safety, and efficacy. Responsibilities typically include designing stability studies, analyzing samples at different time points, and documenting results in compliance with regulatory guidelines (e.g., ICH, FDA). QC Stability professionals work closely with quality control and regulatory teams to ensure data integrity and provide critical information for product shelf-life determination.

What are the typical day-to-day responsibilities of a QC Stability professional?

A QC Stability professional is responsible for managing stability studies on pharmaceutical products, which includes preparing stability samples, testing products at specified intervals, analyzing and documenting results, and ensuring data integrity. This role often involves working closely with cross-functional teams such as quality assurance, production, and research and development to address any findings or deviations. You can expect to spend time in the laboratory conducting tests, as well as at your desk compiling reports and supporting regulatory submissions. The position requires meticulous organization and the ability to handle multiple studies simultaneously, making time management a valuable asset.

What are the key skills and qualifications needed to thrive in the QC Stability position, and why are they important?

To thrive as a QC Stability professional, you need a solid background in chemistry, analytical testing, and good documentation practices, typically supported by a degree in life sciences or related field. Familiarity with laboratory information management systems (LIMS), chromatography software (such as HPLC or GC), and regulatory guidelines like GMP and ICH is essential. Strong attention to detail, problem-solving abilities, and effective communication skills are key soft skills in this role. These competencies ensure accurate data analysis, regulatory compliance, and efficient teamwork in maintaining product quality over time.

What are popular job titles related to Qc Stability jobs in Edison, NJ?

For Qc Stability jobs in Edison, NJ, the most frequently searched job titles are:

What job categories do people searching Qc Stability jobs in Edison, NJ look for?

The top searched job categories for Qc Stability jobs in Edison, NJ are:

What cities near Edison, NJ are hiring for Qc Stability jobs?

Cities near Edison, NJ with the most Qc Stability job openings:

Qc Stability jobs near you
Infographic showing various Qc Stability job openings in Edison, NJ as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $84,190 per year, or $40.5 per hour.

QUALITY CONTROL CHEMIST I

ASPIRE PHARMACEUTICALS INC

Somerset, NJ

Other

Re-posted 9 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.

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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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