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Quality Control Stability Analyst Jobs in California

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

Title: QC Stability Study Coordinator I Summary * With limited supervision, QC Stability Study ... These duties include execution of trend analysis, documentation review, support of deviations (OOS ...

Avid Bioservices

Specialist, Quality Control

Tustin, CA · On-site

$32.30 - $40.38/hr

Your Role: The Quality Control Specialist is an individual contributor who works within the QC ... Prepare Stability Summary of Testing reports, Certificates of Analysis, and Statements of Testing

Avid Bioservices

Specialist, Quality Control

Tustin, CA

$32.30 - $40.38/hr

Your Role: The Quality Control Specialist is an individual contributor who works within the QC ... Prepare Stability Summary of Testing reports, Certificates of Analysis, and Statements of Testing

TekWissen LLC

QC Analyst I

Vacaville, CA · On-site

$20 - $25/hr

Onsite Summary The QC Stability Study Coordinator I is responsible for overseeing stability program ... Review analytical data against established acceptance criteria * Perform technical review of peer ...

Alamar Biosciences

Senior Analyst, Quality Control

Fremont, CA · On-site

$26.25 - $35.25/hr

Perform analytical/functional testing for raw material, in-process/bulk, finish goods, and stability products. * Perform data analysis and generate summary result documentation. * Prepare internal QC ...

Astrix Inc

QC Analyst (Pharma)

Ventura, CA · On-site

$39 - $41/hr

Job type: 6-month contract (possibility of extension or conversion) Position Summary The QC Analyst is responsible for supporting routine laboratory testing, sample management, stability program ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$147K - $171K/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 ...

Grifols

QC Sr. Analyst

Emeryville, CA

$48.23/hr

The Senior QC Analyst will use experience in all analytical assay method training to coordinate and ... Seedstock Stability testing * Cleaning and or Process Validation testing * Analytical Method ...

System One Holdings, LLC

QC Analyst

Novato, CA · On-site

$28 - $32/hr

Job Title: QC Analyst Location: Novato, CA Type: Contract Compensation: $28.00 - $32.00 Work Model: Onsite - onsite Hours: Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview ...

New

GRIFOLS, S.A.

QC Sr. Analyst

Emeryville, CA · On-site

$48.23/hr

The Senior QC Analyst will use experience in all analytical assay method training to coordinate and ... Seedstock Stability testing * Cleaning and or Process Validation testing * Analytical Method ...

System One

QC Analyst

Novato, CA · On-site

$28 - $32/hr

Job Title: QC Analyst Location: Novato, CA Type: Contract Compensation: $28.00 - $32.00 Work Model: Onsite - onsite Hours: Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview ...

New

Arixa Capital

QC Analyst

Los Angeles, CA · On-site

$25.75 - $34.75/hr

Position Overview The QC Analyst is an analytical, process driven, and detail-oriented professional responsible for supporting Arixa Capital's data quality across the loan lifecycle. This role ...

Arixa Capital

QC Analyst

Los Angeles, CA · Hybrid

$25.75 - $34.75/hr

Position Overview The QC Analyst is an analytical, process driven, and detail-oriented professional responsible for supporting Arixa Capital's data quality across the loan lifecycle. This role ...

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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.

QC Analyst I - Vacaville, CA

Unicon Pharma Inc.

Vacaville, CA • On-site

$27.25 - $36.50/hr

Contractor

Re-posted 6 days ago

Job description

Description:

  • Title: QC Stability Study Coordinator I

Summary

  • With limited supervision, QC Stability Study Coordinator, is responsible for the oversight of stability program management in accordance with cGMP regulations.
  • These duties include execution of trend analysis, documentation review, support of deviations (OOS, OOT, OOE) and other laboratory support activities. In conjunction with Quality Control leadership, the QC Stability Study Coordinator works to meet departmental and organizational goals.

Job Responsibilities

  • Review data and assess against established acceptance criteria
  • Perform technical review of peer-generated data
  • Evaluate data to identify trends and/or establish limits
  • Identify discrepancies; provide input to design of quality investigations and CAPA (corrective actions preventive actions) initiatives as needed
  • Identify and troubleshoot technical problems
  • Identify gaps in systems and procedures
  • Receive training
  • Support the maintenance and compliance of operational areas
  • Assure and apply GMP throughout operations
  • Coordinate with customers to support multi-site operational activities
  • Support internal and external audits and regulatory inspections
  • Works to meet schedules, timelines, deadlines
  • Participate in and/or lead group and project teamwork; project and process improvements
  • Stability Protocol Creation
    Stability deviation assessments
  • Routine Master Data Testing Creation
  • Routine Master Data Testing Review
  • Routine and non-routine Out Of Trend linear regression assessments.
  • Annual Product Quality Reviews (APQRs) - Author assistance develop to authoring
  • Time Point Approval assistance
    Change control of various documents
  • Data / Data Table requests / annual report requests (non-routine requests) (e.g.,
    Client monitor requests)
  • Actively participate in various stability related projects
  • Data entry and review
  • Assist with training coordination
  • Assist with Perform other duties as requested by managers to support Quality activities

Job Requirements

  • B.S. /B.A. degree and 1-3 years of experience or an equivalent combination of education and experience. Degrees are preferably in relevant scientific disciplines and experience is in the pharmaceutical or biopharmaceutical industry.
    Strong verbal and written communication skills, ability to organize and present information both formally and informally.
  • Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures.
  • Routinely exercises sound judgment, reasoning and problem solving.
  • Capable of working under limited supervision and determining own short term priorities.