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Quality Control Stability Jobs in Edison, NJ (NOW HIRING)

Tris Pharma

QC Analytical Chemist

Monmouth Junction, NJ · On-site

$90K/yr

... and/or stability sample (ST) samples including dissolution, assay, content/blend uniformity ... QC Analytical Chemist I -Bachelor's Degree in Chemistry or related science field and minimum 1-5 ...

Tris Pharma

QC Analytical Chemist

Monmouth Junction, NJ · On-site

$90K/yr

Performs testing of raw materials, in-process (IP), finished products (FP) and/or stability sample ... QC Analytical Chemist I -Bachelor's Degree in Chemistry or related science field and minimum 1-5 ...

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All JobsQuality Control Stability JobsQuality Control Stability Jobs in Edison, NJ

Quality Control Stability information

See Edison, NJ salary details

$31.6K

$84.2K

$134.1K

How much do quality control stability jobs pay per year?

As of Aug 20, 2026, the average yearly pay for quality control 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 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 are popular job titles related to Quality Control Stability jobs in Edison, NJ?

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

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

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

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

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

Quality Control Stability jobs near you

Associate Scientist, Quality Control

Amneal Pharmaceuticals

Piscataway, NJ • On-site

$65K - $75K/yr

Full-time

Re-posted 7 days ago

Amneal Pharmaceuticals rating

6.7

Company rating: 6.7 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

74th of 86 rated pharmaceutical

Job description

Description:

The Scientist I - QC is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents.


Essential Functions:

  • Performs physical and chemical analysis of raw materials, in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods as applicable, material specifications, using analytical techniques such as IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques adhering to company policies as identified in standard operating procedures (SOPs).
  • Prepares samples for analysis involving thorough cleanliness and complex steps for analysis using chromatographic techniques and other analytical techniques as applicable.
  • Creates and maintains laboratory record documentation (notebooks and computer-based), documents exact steps followed during analysis execution, calculates and reports results in a timely manner.
  • Actively participates in investigation of laboratory results, when required.


Additional Responsibilities:

  • Assists, as and when needed, scientists working in the laboratory.
  • Informs QC Coordinator if chemical or reference standard is expired for removal from laboratory area.
  • Performs calibration of dissolution apparatus, FT-IR, UV-Vis spectrophotometer, HPLC as assigned by the supervisor.
  • Prepares volumetric test solutions following USP or in-house methods for wet chemical tests, standardizes such solutions as required, standardizes API for use as in-house reference standard as assigned.

Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at accommodations@amneal.com. Requests will be handled confidentially and in accordance with applicable laws. 


Education:

  • Bachelor's Degree (BA/BS) Chemistry or related field - Required

Experience:

  • less than one year in Testing of chemicals/pharmaceutical products
  • 1 year or more in Testing of chemicals/pharmaceutical products

Specialized Knowledge:

  • Must possess a working knowledge of analytical chemistry techniques, such as analytical weighing, quantitative transfer, preparation of quantitative solutions, analytical dilutions, spectrophotometric analytical techniques, dissolution and drug release, disintegration, moisture determination (Karl Fischer, Coulometric, LOD), thin-layer chromatographic technique, gas chromatographic techniques, HPLC, and measuring physical parameters (bulk and tapped densities, and particle size by sieve analysis).
  • Must be able to follow compendial (USP/EP/BP/JP) procedures for wet chemical tests.
  • Must understand and apply cGMP requirements applicable to quality control laboratory.

The annual salary for this position ranges from $65,000 to $75,000 per year.  In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills.

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