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Quality Control Stability Manager Jobs in New York

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

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 ...

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 ...

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 ...

QC Chemist

Pearl River, NY · On-site

$55K - $95K/yr

Excellent organization, time management, and communication skills. The main responsibilities for ... Monitors Stability chambers, Photostability chamber, freezers, refrigerators etc. * Performs ...

Quality Control Manager

Manhattan, NY · On-site

$128K - $155K/yr

Manages the activities of the quality control team to ensure that the work product meets the standards as set forth in the contracts and other specification documents. Primary/Essential ...

We are actively seeking a dedicated and results-driven Quality Control Manager. In this role, you will be responsible for developing, implementing, and leading the overall quality strategy to ensure ...

We are actively seeking a dedicated and results-driven Quality Control Manager. In this role, you will be responsible for developing, implementing, and leading the overall quality strategy to ensure ...

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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QUALITY CONTROL CHEMIST I

ASPIRE PHARMACEUTICALS INC

Somerset, NJ

Other

Re-posted 7 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

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