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Quality Control Stability Analyst Jobs in California

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 ...

BioTalent

Quality Control In-Process Analyst

Tustin, CA · On-site

$25.25 - $33.75/hr

Perform QC testing for lot release, stability, development/validation projects, and investigations ... Must have experience with analytical testing, writing reports, GMPs, and regulatory audits. This ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

Us tech Solutions

Quality Control Analyst

Berkeley, CA

$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 ...

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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 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 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. The role often requires knowledge of stability testing, laboratory skills, and regulatory standards.

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, 76% Full Time, 17% Part Time, 5% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution.

QC Sr. Analyst

GRIFOLS, S.A.

Emeryville, CA • On-site

$48.23/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 7 days ago

Key responsibilities

  • Coordinate and perform assays for designated laboratory testing, including protein chemistry, microbiological, and stability testing.

  • Conduct troubleshooting, validation, and technical studies related to assay methods and product testing.

  • Assist with planning and executing operational excellence projects and train staff on test methods.

Grifols rating

6.6

Company rating: 6.6 out of 10

Based on 281 frontline employees who took The Breakroom Quiz

77th of 86 rated pharmaceutical

Job description

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
Grifols Diagnostic Solutions in Emeryville, CA is seeking a Senior QC Analyst. The Senior QC Analyst will use experience in all analytical assay method training to coordinate and perform critical material qualification and maintenance and/or other projects that are in addition to typical release, reference/reagent qualification and/or stability testing. To provide expertise to their designated QC group, and to accurately assess the purity, potency, efficacy, and other performance characteristics for the purpose of supporting both manufacturing and quality assurance in the production, release, and monitoring of established product lines.
To qualify for the Senior QC Analyst role, we are seeking individuals with at least a Bachelor's degree in Biochemistry, Molecular Biology, Immunology with 3 years in a regulated GMP testing laboratory or MS Degree in Science with 1 plus years.
Responsibilities:
  • Coordinate and perform assays for their designated laboratory
    • Routine in-process, final product (antigens) protein chemistry testing for release
    • Routine in-process, final product (antigens) microbiological testing for release of product Routine testing for release of Raw Materials
    • Routine testing for release of Seed Stock
    • Antigen Stability, reference/reagent qualification testing
    • Seedstock Stability testing
    • Cleaning and or Process Validation testing
    • Analytical Method Validation testing
    • Product/Method development testing
  • Use experience and method expertise to conduct troubleshooting
  • May be assigned to assist with OOS Investigations
  • May be assigned to work independently on Validation, and Technical studies
  • May be assigned to assist with the planning and execution of OE projects
  • May be assigned to train staff on test methods
  • Comply Site Environmental Health & Safety (EH&S) requirements

Knowledge, Skills, and Abilities:
  • Must have substantial (three or more) assay testing experience in one of the main areas listed:
    • Protein chemistry methods such as Lowry, Bradford, BCA, SDS-PAGE, Western Blot, HPLC, Amino Acid Analysis, ELISA's and in vitro diagnostic test kits.
    • Microbiological methods such as Microbial Limits Test (bioburden), Sterility, Endotoxin, TOC, Microbial Identification, Contamination testing and Growth Promotion.
    • Bacterial and Yeast Seedstocks testing methods such as microscopic examination, viability, contamination, purity and phenotype testing, DNA Plasmid isolation and restriction digest testing.
    • Environmental/Utility/facility Monitoring testing such as Sampling of and testing of manufacturing water by membrane filtration, viable and non-viable particulate testing of facilities and utilities, viable (surface) monitoring of manufacturing facilities, personnel and biological hoods, moisture and oil content testing of compressed gases
    • Analytical/Microbiological Method Validation testing such as Bacteriosis and Fungistasis, linearity, specificity and robustness tests in protein chemistry, microbiology or complendial test methods
    • Assay trouble shooting experience in their expert area
    • Pharmacoepeial (compendial) test methods for Raw Materials such as, but not limited to; melting point, loss on drying, color and appearance, identity by FTIR, heavy metals, arsenic, residual solvents, chloride, sulphate, insoluble matter
  • Proficient in MS Word, MS Powerpoint and MS Excel software
  • Must be familiar with GMP's and Quality System Regulations (QS Regs)
  • Must have good time management, effectively prioritizing tasks for completion
  • Individual must work in an ethical manner and ensure employees follow Grifols ethics and compliance guidelines.
  • Must meet the two (2) mission critical competencies: 1) Customer Focus 2)Function/Technical Skills

Education: Bachelor's degree in Biochemistry, Molecular Biology, Immunology with 3 years or MS degree in science with 1 plus years.
Experience: At least 3 years' experience in a regulated GMP testing laboratory
Equivalency:
Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level typically requires an Associate's degree plus 2 years of experience, an equivalent could include 4 years of experience or a bachelor's degree.
The estimated pay scale for Senior QC Analyst role based in Emeryville, California, is $38.58 per hour to $48.23 per hour. Additionally, the position is eligible to participate in up to 5% of the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, life insurance, PTO, paid holidays and up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us!
Third Party Agency and Recruiter Notice:
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location: NORTH AMERICA : USA : CA-Emeryville:USEMV - Emeryville CA-Headquarters
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