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Quality Control Stability Jobs (NOW HIRING)

QC Analyst I

Vacaville, CA · On-site

$20 - $25/hr

Onsite Summary The QC Stability Study Coordinator I is responsible for overseeing stability program management in compliance with cGMP regulations, with limited supervision. This role includes ...

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 ...

Scientist - Quality Control (QC)

Franklin Township, NJ · On-site

$70 - $90/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Control Location: Somerset, New Jersey FLSA Status: Exempt Employment Type: Full-Time ... Perform analytical testing of raw materials, in-process materials, finished products, and stability ...

New

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 ...

Senior Expert Stability

East Hanover, NJ · On-site

$118K/yr

  • Medical

  • Retirement

  • PTO

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

Quality Control QC Lead

Warren, OH · On-site

$28 - $32/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Relocation bonus Quality Control (QC) Lead $26.07 - $31.39 an hour - Temporary, Part-time, ... stability and growth. The successful candidate will be a quality champion who thrives in a fast ...

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 ...

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 ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

Quality Control

Bruning, NE

$21 - $27/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

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.

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

Showing results 21-40

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 Aug 19, 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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The most popular types of Quality Control Stability jobs are:

What states have the most Quality Control Stability jobs?

States with the most job openings for Quality Control Stability jobs include:

What job categories do people searching Quality Control Stability jobs look for?

The top searched job categories for Quality Control Stability jobs are:

QC Analyst I

TekWissen LLC

Vacaville, CA • On-site

$20 - $25/hr

Temporary

Re-posted 23 days ago


Job description

Overview:  
 
TekWissen group is a workforce management provider throughout the USA and many other countries in the world. Our client is a leading biotechnology company that combines technological expertise with world-class manufacturing and scientific insight to support the delivery of innovative medicines for a wide range of diseases. Specializing in pharmaceutical ingredients, bioscience, biopharmaceuticals, custom manufacturing, and cell and gene therapy, the company provides comprehensive services across the pharmaceutical, biotech, and life sciences sectors. It supports every stage of drug development, from early research to commercial production, and offers solutions in biologics, small molecules, and specialty ingredients. Committed to quality and innovation, the company serves as a critical partner in advancing therapeutic solutions and streamlining complex manufacturing processes, with a global presence that ensures access to scalable, flexible, and compliant technical expertise.
 
 
Job Title:         QC Analyst
Location:         Vacaville, CA
Duration:        6 months 
Job Type:        Temporary Position
Work Type:    Onsite
 
 
Summary
 
The QC Stability Study Coordinator I is responsible for overseeing stability program management in compliance with cGMP regulations, with limited supervision. This role includes execution of trend analysis, documentation review, deviation support (OOS, OOT, OOE), and general laboratory support activities. The coordinator works closely with Quality Control leadership to achieve departmental and organizational objectives.
 
Key Accountabilities:
  • Review analytical data against established acceptance criteria
  • Perform technical review of peer-generated data
  • Evaluate data to identify trends and establish limits
  • Conduct routine and non-routine Out of Trend (OOT) linear regression assessments
  • Support deviations including OOS, OOT, and OOE investigations
  • Provide input into quality investigations and CAPA initiatives
  • Identify and troubleshoot technical issues
  • Identify gaps in systems and procedures
  • Develop Stability Protocols
  • Conduct stability deviation assessments
  • Create and review Routine Master Data Testing
  • Assist in Annual Product Quality Reviews (APQRs) authoring
  • Support time point approval activities
  • Manage change control documentation
  • Handle data table requests and annual report requests (including client monitor requests)
  • Participate in stability-related projects and process improvement initiatives
  • Perform data entry and review
  • Support training coordination
  • Maintain GMP compliance in all operational areas
  • Coordinate with customers for multi-site operational support
  • Support internal audits, external audits, and regulatory inspections
  • Work effectively to meet schedules, timelines, and deadlines
  • Participate in and/or lead cross-functional project teams
  • Perform additional quality-related duties as assigned
Required Qualifications
  • B.S./B.A. degree in a relevant scientific discipline
  • 1–3 years of experience in the pharmaceutical or biopharmaceutical industry (or equivalent combination of education and experience)
  • Knowledge of cGMP regulations and quality systems
  • Experience in stability program management
  • Exposure to regulatory inspections and audit support
  • Experience with CAPA, deviation investigations, and change control processes
  • Knowledge of trend analysis and statistical data evaluation
  • Experience supporting multi-site operations
  • Familiarity with APQR documentation and authoring support
  • Strong verbal and written communication skills
  • Ability to organize and present information formally and informally
  • Working knowledge of scientific theories, principles, and analytical/biological testing techniques
  • Strong problem-solving, reasoning, and analytical skills
  • Ability to exercise sound judgment
  • Capable of working independently with limited supervision
  • Ability to prioritize short-term tasks effectively
TekWissen® Group is an equal opportunity employer supporting workforce diversity.

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 


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About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

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