ZipRecruiter

Log In

1

Quality Control Stability Jobs in New York (NOW HIRING)

Novartis

Senior Expert Stability

East Hanover, NJ

$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 ...

Careers at RK Pharma Inc.

QC Chemist

Pearl River, NY · On-site

$55K - $95K/yr

Monitors Stability chambers, Photostability chamber, freezers, refrigerators etc. * Performs ... Train other QC chemists in a timely manner on all the general Laboratory SOPs and test methods.

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

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

$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

$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 ...

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 ...

next page

Showing results 1-20

All JobsQuality Control Stability JobsQuality Control Stability Jobs in New York

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 the most commonly searched types of Quality Control Stability jobs in New York? The most popular types of Quality Control Stability jobs in New York are:
What are popular job titles related to Quality Control Stability jobs in New York? For Quality Control Stability jobs in New York, the most frequently searched job titles are:
What job categories do people searching Quality Control Stability jobs in New York look for? The top searched job categories for Quality Control Stability jobs in New York are:
What cities in New York are hiring for Quality Control Stability jobs? Cities in New York with the most Quality Control Stability job openings:
Quality Control Stability jobs near you

QUALITY CONTROL CHEMIST I

ASPIRE PHARMACEUTICALS INC

Somerset, NJ

Other

Posted 16 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

FacebookTwitter

View All Aspire Pharmaceuticals Jobs