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Quality Control Stability Analyst Jobs in California

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 ...

Quality Control Analyst III in Camarillo, CA Build your future at Curia, where our work has the ... Routine functions include testing of raw materials, in-process, end product, and stability samples.

Quality Control Analyst III

Camarillo, CA · On-site

$85K - $106K/yr

Quality Control Analyst III in Camarillo, CA Build your future at Curia, where our work has the ... Routine functions include testing of raw materials, in-process, end product, and stability samples.

QC Analyst III

Pomona, CA · On-site

$33 - $36/hr

QC Analyst III Working from Home Opportunities Available Salary Range: $33 t0 $36/ hour, DOE We are looking for a certified licensed appraiser, either Residential, Commercial, or both to join our ...

QC Analyst III (Pharma)

Ventura, CA · On-site

$58 - $60/hr

Job type: 6-month contract (possibility of extension or conversion) Job Summary The QC Analyst III ... This role provides technical leadership for analytical activities, stability programs, and ...

QC Analyst II

Vacaville, CA · On-site

$28/hr

Position: QC Analyst II Location: Vacaville, CA (Onsite) Pay Rate : $28/hr. on W2 Summary Under limited supervision, the QC Analyst II is responsible for performing direct materials testing in ...

... product release, stability, method lifecycle management, and ensure laboratory readiness for ... Lead QC analytical testing activities supporting clinical and commercial DS and DP manufacturing ...

QC DIRECTOR

Rocklin, CA · On-site

$180 - $240/hr

... stability samples, the full lifecycle of analytical methods, instrument asset management, and ... Build and manage the QC team, department budget and lab EHS governance. In addition, provide ...

QC DIRECTOR

Santa Rosa, CA · On-site

$180 - $240/hr

... and stability samples, full lifecycle of analytical methods, instrument asset management ... Build and manage the QC team, department budget and lab EHS governance. In addition, provide ...

Showing results 41-60

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:
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.

Analyst (HPLC), Quality Control

Avid Bioservices

Tustin, CA

$25.76 - $32.21/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 6 hours ago


Job description

Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
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 strong background in HPLC and supports/leads continuous improvement initiatives.
Key Responsibilities:
  • Perform and review routine assays for HPLC and CE (Capillary Electrophoresis) with strict adherence to written analytical test procedures.
  • Perform aseptic sampling, visual inspection, gowning and working in clean room areas, 5S methodology.
  • Review, revise and write test methods, standard operating procedures and perform trending analysis.
  • In addition to performing QC testing, the Analyst may be designated as study lead for validation projects, investigations and method development projects.
  • Other functions include, but are not limited to, writing study protocols and reports; training other analysts; working with other departments in developing, revising and implementing QC procedures and policies.
  • Knowledgeable of company cGMPs as well as industry regulations that apply to all job functions.
  • Participate in regulatory inspections to ensure laboratory is in compliance with current Good Manufacturing Practices.
  • Demonstrate and provide evidence to FDA officials that the laboratory operations conform to code of federal regulation.
  • Support continuous improvement initiatives by ensuring training relating to test methods, standard operating procedures, are up to date to comply with current good manufacturing practices.
  • Utilize Instruments software to perform calculations to minimize errors and eliminate time allocation for manual calculations.
  • Perform other duties as assigned.
Minimum Qualifications:
  • BS in chemistry or biology or related field plus 2-4 years industry experience in a QC or analytical lab, or equivalent combination of education/experience.
  • Experience with analytical testing and equipment, writing reports/procedures/specifications, GMPs and regulatory audits are essential.
  • Must have strong HPLC, Analytical Biochemistry and Chemistry experience.
  • Must also have experience with most if not all of the following: protein characterization, electrophoresis, chromatography (normal phase, reverse phase, size exclusion, ion exchange, etc), aseptic techniques, assay and validation/qualification.
Position Type/Expected Hours of Work:
This role is a full-time onsite position. Days and hours of work are Monday through Friday, 8:00am to 5:00pm PST unless otherwise stated by Supervisor. The employee must also have the ability to work overtime and/or weekends when necessary.
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $25.76 to $32.21 hourly annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:

In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.
Employment Type: Full-Time