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Quality Control Stability Jobs (NOW HIRING)

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

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

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

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 ...

Metal-Tech Partners

Quality Control

Bruning, NE · On-site

$21 - $27/hr

Quality Control Specialist Location: [Insert Location] Company: Metal-Tech Partners Metal-Tech ... We offer a competitive compensation package, long-term employment stability, and a positive ...

Actalent

QC Manager

West Point, PA

This role oversees raw material, finished product, and stability testing, drives laboratory compliance and operational efficiency, and aligns QC capabilities with current and future business needs.

Stand-By Personnel

Quality Control

Catoosa, OK · On-site

$24/hr

Quality Control Inspector Pay: $24+/hour Shift: Night Shift Position: Temp-to-Hire Location ... and stability. Additional Benefits: * $50 Advance: Available after your first day of work.

Stand-By Personnel

Quality Control

Catoosa, OK · On-site

$24/hr

Quality Control Inspector Pay: $24+/hour Shift: Night Shift Position: Temp-to-Hire Location ... and stability. Additional Benefits: * $50 Advance: Available after your first day of work.

Actalent

QC Manager

West Point, PA

This role oversees raw material, finished product, and stability testing, drives laboratory compliance and operational efficiency, and aligns QC capabilities with current and future business needs.

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.

Stand-By Personnel

Quality Control

Catoosa, OK · On-site

$24/hr

Quality Control Inspector Pay: $24+/hour Shift: Night Shift Position: Temp-to-Hire Location ... and stability. Additional Benefits: * $50 Advance: Available after your first day of work.

Stand-By Personnel

Quality Control

Owasso, OK · On-site

$17.50/hr

Maintain accurate records, including quality control logs, inspection reports, and food safety ... and stability. Additional Benefits: * $50 Advance: Available after your first day of work.

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Quality Control Stability information

See salary details

$30.5K

$81.3K

$129.5K

How much do quality control stability jobs pay per year?

As of Sep 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 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.
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Quality Control Stability jobs near you

Director, Quality Control

Redwood City, CA • On-site

Corcept Therapeutics
Biotechnology Research and Development • 51 - 200 employees
Learn more about Corcept Therapeuticsexternal

$215K - $253K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

The position will provide strategic and organizational leadership for the Quality Control function supporting Corcept's development and commercial programs. This position will have end-to-end oversight of all stability programs at contract laboratories and will author the stability sections of regulatory filings. This position will partner closely with the Sr Director of Analytical Development & Quality Control (ADQC) to continuously strengthen, expand, and scale the QC function, with increasing responsibility across broader QC activities.  

Responsibilities:

  • Lead the QC function with primary responsibility for the design, execution, and oversight of stability programs
  • Oversee stability studies conducted at external laboratories, ensuring compliance, data integrity, and timely execution
  • Review, trend, and maintain stability data. Alert the project team of any adverse trending
  • Collaborate with vendors and internal cross-functional teams to ensure that out-of-trend and out-of-specification results are addressed promptly
  • Provide stability study progress summaries to project teams and ensure that stability reports are completed promptly
  • Oversee internal documentation to support retest periods and shelf-life extension based on data generated from ongoing stability studies
  • Support analytical project leads in preparation of batch analysis; author and review stability sections required for regulatory submissions
  • Support analytical project leads in reviewing method validation protocols, reports, analytical method and test data
  • Manage data review qualifications of contract laboratories
  • Partner with the Sr Director of ADQC to build and enhance QC capabilities, infrastructure, and processes, with the expectation to progressively expand scope into broader QC oversight

Preferred Skills, Qualifications or Technical Proficiencies:

  • Strong technical expertise in stability study design, execution, and interpretation
  • Proven experience managing stability programs supporting late-stage development and global regulatory submissions
  • Experience in managing analytical testing in an outsourced environment
  • Experience in using statistical tools for data trend analysis and projection of drug substance retest period or drug product shelf-life
  • Excellent communication and collaboration skills with proven ability to work effectively with other functional groups

Preferred Education and Experience:

  • S. in relevant scientific discipline. Advanced degree in Analytical Chemistry or other relevant disciplines
  • 10+ years QC experience in the pharmaceutical industry

The pay range that the Company reasonably expects to pay for this headquarters-based position is $215,300-$253,200; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

 Applicants must be currently authorized to work in the United States on a full-time basis.

Apply