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Qc Stability Jobs (NOW HIRING)

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$147K - $171K/yr

This individual will collaborate with QC members in a highly collaborative and cross-functional environment. The ideal candidate will apply strong stability experience, ensure compliant operations ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$134K - $162K/yr

This individual will collaborate with QC members in a highly collaborative and cross-functional environment. The ideal candidate will apply strong stability experience, ensure compliant operations ...

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 ...

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 ...

Tolmar

Quality Control Planner

Fort Collins, CO

$19.25 - $26.50/hr

The QC Planner is responsible for the management, planning and coordination of samples in the QC ... Ensure the stability pulls schedule are mitigated and designed with the most efficient test ...

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 ...

Tolmar Inc.

Quality Control Planner

Fort Collins, CO

$19.25 - $26.50/hr

The QC Planner is responsible for the management, planning and coordination of samples in the QC ... Ensure the stability pulls schedule are mitigated and designed with the most efficient test ...

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 Holdings, LLC

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 ...

Tolmar

Quality Control Planner

Fort Collins, CO · On-site

$39 - $40.50/hr

The QC Planner is responsible for the management, planning and coordination of samples in the QC ... Ensure the stability pulls schedule are mitigated and designed with the most efficient test ...

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All JobsQc Stability Jobs

Qc Stability information

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$30.5K

$81.3K

$129.5K

How much do qc stability jobs pay per year?

As of Jul 12, 2026, the average yearly pay for qc stability in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

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 is a QC Stability job?

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.

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Qc Stability jobs near you
Quality Control Lab Supervisor- New York City

Quality Control Lab Supervisor- New York City

Prime Matter Labs

Long Island City, NY • On-site

$70K - $85K/yr

Full-time

Posted 24 days ago

Job description

JOB PURPOSE
The Quality Control Lab Supervisor (QC Bulk Supervisor) is responsible for overseeing all QC laboratory and in-process
testing activities to ensure raw materials and bulk products meet company quality standards, regulatory requirements,
and customer expectations. This role provides leadership to the QC team, drives continuous improvements, ensures
compliance with cGMP and ISO standards, and partners with cross-functional teams to resolve quality-related issues.
DUTIES & RESPONSIBILITIES
• Lead and supervise the Quality Control stability, raw materials and bulk departments, including chemists, technicians,
and analysts, ensuring optimal performance and adherence to quality standards.
• Oversee all QC activities, including raw material and bulk testing, ensuring accuracy, timeliness, and compliance with
established protocols.
• Develop, implement, and maintain QC policies, procedures, and work instructions in compliance with cGMP, FDA, and
ISO regulations.
• Review and approve test results, certificates of analysis, and related quality documentation prior to product release.
• Manage laboratory investigations for out-of-specification (OOS) and out-of-trend (OOT) results, ensuring root cause
analysis and corrective/preventive actions are implemented.
• Collaborate with Quality Assurance, R&D, Manufacturing, and Supply Chain to address quality concerns and drive
product improvements.
• Oversee method validations, stability studies, and instrument calibration/maintenance programs to ensure accuracy
and reliability of test results.
• Ensure all QC staff are properly trained on lab procedures, safety requirements, and Good Documentation Practices.
• Monitor laboratory performance metrics and implement process improvements to optimize efficiency and cost-
effectiveness.
• Support the QC department budget, including resource planning and procurement of lab supplies and equipment.
• Stay current on regulatory and industry standards, implementing changes as necessary to maintain compliance.
• Prepare and present regular reports on QC performance, trends, and quality metrics to senior leadership.
• Support internal, customer, and regulatory audits by providing QC data, records, and responses to findings.
QUALIFICATIONS
• Bachelor's degree in Chemistry, Biochemistry, or a related scientific field (Master's degree preferred).
• 5+ years of experience in quality control or analytical testing, with at least 3 years in a supervisory or management role.
• Strong knowledge of cGMP, FDA, ISO, and other regulatory guidelines.
• Experience in cosmetics, pharmaceuticals, or food manufacturing environments preferred.
• Proficiency with laboratory instrumentation (e.g., pH meter, Viscometer, FTIR) and method development/validation.
• Excellent leadership, analytical, and problem-solving skills.
• Strong organizational skills and the ability to manage multiple priorities in a fast-paced environment.
• Proficient in MS Office and laboratory information management systems (LIMS).
PHYSICAL REQUIREMENTS
• Fully on-site expectation, 5 days a week for one shift only.
• Ability to stand for extended periods while working in the lab.
• Capability to lift up to 25 lbs. when handling lab equipment or materials.
• Manual dexterity for operating laboratory instruments and handling small samples.
• Must be able to wear appropriate personal protective equipment (PPE) such as lab coats, gloves, and safety glasses.
Salary Range: $70K to $85K
At Prime, we believe that a diverse, equitable and inclusive workplace makes us a more relevant, more competitive, and more resilient company. We welcome people from all backgrounds, ethnicities, cultures, and experiences. Prime is an equal opportunity employer.

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