ZipRecruiter

Log In

1

Quality Control Stability Analyst Jobs in California

TekWissen LLC

Quality Control Analyst

Vacaville, CA · On-site

$20 - $25/hr

Job Title: QC Associate / Quality Control Analyst I Location: Vacaville, CA - 95688 Duration: 6 Months Job Type: Temporary Assignment Work Type: Onsite Summary With limited supervision, the QC ...

Arixa Capital

QC Analyst

Los Angeles, CA · Hybrid

$25.75 - $34.75/hr

The QC Analyst will analyze data for consistency, identify discrepancies, correct mistakes, and provide feedback and training to the operational teams to avoid future inconsistencies. This position ...

Us tech Solutions

Quality Control Analyst

Berkeley, CA · On-site

$29.75 - $40/hr

Quality Control Analyst Duration: 12 Months Location: Berkeley, CA 94710 Biological Development Assay Development, Quality Control (BD AD-QC) Position summary: The purpose of this position is to ...

Us tech Solutions

Quality Control Analyst

Berkeley, CA · On-site

$29.75 - $40/hr

Quality Control Analyst Duration: 12 Months Location: Berkeley, CA 94710 Biological Development Assay Development, Quality Control (BD AD-QC) Position summary: The purpose of this position is to ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$134K - $162K/yr

Primary responsibility will include managing stability studies for individual projects and stability data analysis. This individual will collaborate with QC members in a highly collaborative and ...

Qnity

Entry-Level Quality Control (QC) Analyst

Hayward, CA · On-site

$27.50 - $37/hr

Job Summary The QC Analyst is responsible for performing routine laboratory testing and supporting qualitycontrol activities to ensure products meet established specifications. This entry-level role ...

Talent Software Services, Inc

QC Analyst

Novato, CA · On-site

$28.25 - $37.75/hr

PURPOSE The Quality Control Analytical In-Process (QCA-IP) Analyst is responsible for performing analytical test methods on in-process intermediates and varying stages of drug products under minimal ...

AllSTEM Connections

Quality Control Analyst I

Camarillo, CA · On-site

$82K - $86K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

... QC laboratory testing using pH, Osmolality, FT-IR, for in-process, finished product ... and stability samples testing. • Assist with sample management activities including but not ...

Nova Pneuma, Inc.

QC Analyst II

Fremont, CA · On-site

$41/hr

Provide timely analyses to support manufacturing and stability. This includes routine analyses of ... Knowledge of validation requirements for QC methods and regulatory guidelines Education and ...

Alexza Pharmaceuticals

QC Analyst II

Fremont, CA · On-site

$41/hr

Provide timely analyses to support manufacturing and stability. This includes routine analyses of ... Knowledge of validation requirements for QC methods and regulatory guidelines Education and ...

Avid Bioservices

Analyst (ELISA), Quality Control

Tustin, CA · On-site

$26.73 - $35.63/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... and stability studies. You'll also have a chance to contribute to continuous improvement ... in trending analysis. Alongside regular QC testing, you may be entrusted as a study Lead for ...

Avid Bioservices

Analyst (HPLC), Quality Control

Tustin, CA · On-site

$25.76 - $32.21/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Analyst (HPLC), Quality Control will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment. This position requires a ...

previous pagenext page

Showing results 21-40

All JobsQuality Control Stability Analyst JobsQuality Control Stability Analyst Jobs in California

Quality Control Stability Analyst information

What is a quality control stability analyst?

Quality Control Stability Analysts are professionals responsible for testing and evaluating the stability of pharmaceutical products over time. They design, conduct, and interpret experiments to ensure products maintain their safety, potency, and quality throughout their shelf life. Their work is crucial for regulatory compliance, as they document and report stability data according to industry standards and guidelines. These analysts often work in laboratory environments and collaborate closely with quality assurance and manufacturing teams.

What are the key skills and qualifications needed to thrive as a quality control stability analyst?

To thrive as a Quality Control Stability Analyst, you need a solid background in chemistry or related sciences, familiarity with Good Laboratory Practices (GLP), and often a relevant bachelor's degree. Experience with laboratory instrumentation such as HPLC, GC, and LIMS, along with knowledge of regulatory guidelines like ICH and FDA, is typically required. Attention to detail, strong organizational skills, and effective communication are critical soft skills in this role. These competencies ensure accurate data analysis, compliance with regulations, and reliable stability testing to maintain product quality and safety.

What is the difference between Quality Control Stability Analyst vs Quality Control Analyst?

AspectQuality Control Stability AnalystQuality Control Analyst
CertificationsGMP, GLP, relevant laboratory certificationsGMP, GLP, relevant laboratory certifications
Work EnvironmentPharmaceutical, biotech labs focusing on stability testingManufacturing labs, quality testing environments
Job FocusMonitoring product stability over time, data analysis for stability programsPerforming routine quality tests, raw material and finished product testing

The main difference is that a Quality Control Stability Analyst specializes in stability testing and data analysis related to product shelf life, while a Quality Control Analyst performs general quality testing. Both roles require similar certifications and work in related environments, but their focus areas differ within the quality assurance process.

How much does a quality control stability analyst earn?

A quality control stability analyst typically earns between $50,000 and $80,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced analysts with certifications can earn higher salaries. Compensation often includes benefits such as health insurance and paid time off.

What are some typical challenges faced by quality control stability analysts, and how can they be addressed?

Quality Control Stability Analysts often face challenges such as managing multiple projects with tight timelines, accurately interpreting stability data, and ensuring compliance with stringent regulatory requirements. Balancing the need for meticulous documentation with the fast-paced nature of product development can also be demanding. To address these challenges, analysts benefit from strong organizational skills, effective communication with cross-functional teams (like R&D and production), and ongoing training on evolving industry standards and regulatory guidelines.
What are popular job titles related to Quality Control Stability Analyst jobs in California? For Quality Control Stability Analyst jobs in California, the most frequently searched job titles are:
What job categories do people searching Quality Control Stability Analyst jobs in California look for? The top searched job categories for Quality Control Stability Analyst jobs in California are:
What cities in California are hiring for Quality Control Stability Analyst jobs? Cities in California with the most Quality Control Stability Analyst job openings:
Quality Control Stability Analyst jobs near you
Infographic showing various Quality Control Stability Analyst job openings in California as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, 2% Temporary, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.

Quality Control Analyst

TekWissen LLC

Vacaville, CA • On-site

$20 - $25/hr

Contractor

Re-posted 26 days ago

Job description

Overview:  

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.   Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.  

Job Title:       QC Associate / Quality Control Analyst I
Location:       Vacaville, CA - 95688
Duration:       6 Months
Job Type:       Temporary Assignment     
Work Type:   Onsite

Summary
 
With limited supervision, the QC Associate I is responsible for performing direct materials testing in compliance with cGMP regulations. The role involves executing laboratory testing, reviewing and trending data, supporting investigations (OOS, OOT, OOE), and contributing to laboratory operations and quality objectives. The position works closely with Quality Control leadership to meet departmental and organizational goals.

Responsibilities

  • Perform basic to moderately complex laboratory testing in compliance with GMP requirements
  • Review, analyze, and assess test data against established acceptance criteria
  • Conduct technical review of peer-generated data
  • Perform trend analysis and assist in establishing limits
  • Identify discrepancies and support quality investigations and CAPA initiatives
  • Troubleshoot technical and testing-related issues
  • Identify gaps in systems, procedures, and laboratory practices
  • Participate in assay transfer, assay validation, and method-related activities
  • Perform equipment qualification, calibration, and routine maintenance
  • Prepare and maintain standards, controls, stocks, cultures, and reagents per procedures
  • Ensure GMP compliance across laboratory operations
  • Support internal and external audits and regulatory inspections
  • Coordinate with internal customers to support multi-site operations
  • Meet assigned schedules, timelines, and deadlines (95% on-time performance expectation)
  • Participate in or lead team projects, process improvements, and continuous improvement initiatives
  • Write protocols, reports, and technical documentation under limited supervision
  • Provide and receive training as required
  • Perform additional duties as assigned to support Quality activities
Required Skills
  • Bachelor’s degree (B.S./B.A.) in a relevant scientific discipline with 1–3 years of industry experience OR
  • Master’s degree with at least 1 year of relevant experience
  • Experience in the pharmaceutical or biopharmaceutical industry
  • Hands-on experience with analytical and/or biological testing procedures
  • Strong understanding of cGMP regulations and quality systems
  • Experience with OOS, OOT, and OOE investigations
  • Exposure to assay transfer, assay validation, and method lifecycle activities
  • Experience supporting regulatory inspections (FDA, EMA, etc.)
  • Familiarity with trend analysis and data integrity practices
  • Prior involvement in process improvement or cross-functional projects
  • Experience working in multi-site or global operational environments
  • Ability to apply scientific principles, theories, and techniques in a QC environment
  • Strong verbal and written communication skills
  • Sound judgment, analytical thinking, and problem-solving abilities
  • Ability to work independently with limited supervision and manage short-term priorities
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. 

TekWissen logo

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

Social media

Twitter

View All TekWissen Jobs