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Quality Control Stability Jobs (NOW HIRING)

Vaxcyte

Stability Manager

San Carlos, CA

$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 ...

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 · On-site

$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

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 ...

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 ...

Abzena Inc.

QC Manager

San Diego, CA · On-site

$120K - $150K/yr

We are seeking a highly experienced Quality Control (QC) Manager to lead cGMP QC operations ... Stability studies (ICH-compliant programs) * Testing associated with Qualification/Validation of ...

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Quality Control Stability information

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$30.5K

$81.3K

$129.5K

How much do quality control stability jobs pay per year?

As of Jul 9, 2026, the average yearly pay for quality control 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 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.
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What states have the most Quality Control Stability jobs? States with the most job openings for Quality Control Stability jobs include:
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Quality Control 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

Re-posted 22 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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