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Method Validation Jobs in California (NOW HIRING)

Merck Group

Principal Scientist

Carlsbad, CA · On-site

  • Medical

  • Retirement

  • PTO

Define and drive the method validation/transfer strategy, including relevant considerations (e.g. ddPCR, qPCR, HPLC, ELISA, CE-SDS, FTIR, Gel Electrophoresis, etc.) with auditable documentation.

krg technology inc

Manufacturing Engineer

Temecula, CA · On-site

$72K - $93K/yr

Experience in Test Method validation & Inspection Method validation. * Knowledge in Tolerance analysis & GD&T. * Interface with vendors for procurement. * Knowledge Cp, Cpk, and SPC to improve ...

Talent Software Services, Inc

QC Analyst

Novato, CA · On-site

$28.25 - $37.75/hr

Protein determination by A280, Bradford, UV Absorbance, Enzyme activity, HPLC/UPLC, and method validation. CHARACTERISTICS Functional activities may include: performing a wide variety of analytical ...

5AM Ventures

Analytical Scientist

Emeryville, CA · On-site

$140K - $170K/yr

Demonstrated expertise in bioanalytical method development, validation, and data interpretation within a quality management system (i.e. GLP / GMP) * Strong understanding of both: * Instrumental ...

Astrix Inc

QC Analyst III (Pharma)

Ventura, CA · On-site

$58 - $60/hr

Participate in and support analytical method validations, verifications, and transfers. * Evaluate and trend analytical data to identify quality issues, process improvements, and potential risks.

Trelleborg

Metrology Technician

Paso Robles, CA

$29.92 - $35.57/hr

Setup and conduct test method validation for variable and attribute test method validation activities, including sample creation, developing test method work instructions * In coordination with site ...

Codexis

Sr. Scientist, Quality Control

Redwood City, CA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Sr. Scientist in Quality Control will be leading analytical method transfer and validation for oligonucleotide therapeutic and enzyme products. This role serves as a subject matter expert for ...

5AM Ventures

Analytical Scientist

Emeryville, CA

$140K - $170K/yr

Demonstrated expertise in bioanalytical method development, validation, and data interpretation within a quality management system (i.e. GLP / GMP) * Strong understanding of both: * Instrumental ...

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Showing results 21-40

All JobsMethod Validation JobsMethod Validation Jobs in California

Method Validation information

See California salary details

$22

$51

$77

How much do method validation jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for method validation in California is $51.32, according to ZipRecruiter salary data. Most workers in this role earn between $38.89 and $62.40 per hour, depending on experience, location, and employer.

What is a method validation?

A Method Validation job involves assessing and verifying analytical methods to ensure they produce reliable, accurate, and reproducible results. Professionals in this role typically work in pharmaceutical, biotechnology, or chemical industries, following regulatory guidelines such as ICH, USP, or FDA requirements. Their responsibilities include designing validation protocols, performing experiments, analyzing data, and documenting results. Method validation ensures compliance with industry standards and guarantees product quality and safety.

What does a method validation do?

As a Method Validation professional, you will design, conduct, and document experiments to confirm that laboratory methods produce accurate and reproducible results under specified conditions. Typical daily tasks include preparing protocols, running validation samples, analyzing data, and preparing comprehensive validation reports for internal or regulatory review. You’ll work closely with scientists, quality assurance teams, and regulatory specialists to ensure compliance with industry standards. This collaborative environment provides opportunities to contribute to critical product development stages and to build expertise that supports career progression into quality management, regulatory affairs, or advanced analytical roles.

What are the key skills and qualifications needed for method validation?

To excel in Method Validation, a strong background in analytical chemistry, laboratory techniques, and scientific data analysis is typically required, often supported by a degree in chemistry, biochemistry, or a related field. Familiarity with validation protocols, industry regulations (such as GLP, GMP, or ISO standards), and analytical instrumentation (e.g., HPLC, GC, MS) is essential. Strong attention to detail, problem-solving skills, and effective collaboration and documentation abilities help professionals thrive in this position. These skills are vital to ensure that laboratory methods are reliable, regulatory-compliant, and suitable for their intended purposes.

What are the most commonly searched types of Method Validation jobs in California?

The most popular types of Method Validation jobs in California are:

What are popular job titles related to Method Validation jobs in California?

For Method Validation jobs in California, the most frequently searched job titles are:

What job categories do people searching Method Validation jobs in California look for?

The top searched job categories for Method Validation jobs in California are:

Method Validation jobs near you
Infographic showing various Method Validation job openings in California as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 5% Part Time, 2% Temporary, and 6% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $106,736 per year, or $51.3 per hour.

Mechanical / Biomedical Engineer - Combination Products Test Methods & Validation (GMP, Gage R&R, Au

3 Key Consulting

Thousand Oaks, CA • Hybrid

$42 - $46/hr

Full-time

Re-posted yesterday

Job description

Job Title:   Mechanical / Biomedical Engineer – Combination Products Test Methods & Validation (GMP, Gage R&R, Auto-Injectors) - (JP15464)
Location: Thousand Oaks, CA. 91320 (Hybrid)
Employment Type: Contract
Business Unit: Physical Testing Systems Development
Duration: 18+ months (with likely extensions and/or conversion to permanent)
Posting Date: 06/16/26
Pay Rate: $42 - $46/hour W2
Notes: Only qualified candidates need apply.  Candidates local or open to relocating to Thousand Oaks are welcomed. Hybrid. 
3 Key Consulting is hiring a Mechanical / Biomedical Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
The ideal candidate is a Mechanical or Biomedical Engineer with a Bachelor's degree and 1–3 years of industry experience, preferably within the pharmaceutical, medical device, or biomedical sectors. Candidates should possess hands-on experience with statistical analysis, Gauge R&R studies, and optical measurement systems, along with a working knowledge of CAD/SolidWorks for basic mechanical designs and test fixtures. Strong technical writing skills and familiarity with GMP documentation practices are essential. The successful candidate will be a motivated self-starter who enjoys solving technical challenges, learning new technologies, and working effectively both independently and within cross-functional teams.
This position supports the Combination Product Operations MS&T – Physical Sciences & Engineering (PSE) organization and involves assisting senior engineers with the initiation, design, execution, and delivery of engineering projects. Responsibilities include the development, validation, and lifecycle management of GMP physical test methods, integrated testing equipment, and test methods for auto-injectors and primary containers. The engineer will gather user requirements, develop technical documentation, perform engineering studies, assess automated testing systems, conduct field evaluations of existing equipment, and provide engineering recommendations to support project objectives and continuous improvement initiatives.
The ideal candidate has a passion for analytics, modeling, and technology, with the ability to organize information from multiple sources and transform it into well-structured deliverables. This role offers opportunities to apply engineering and data-driven approaches to improve decision-making, optimize testing processes, and support innovation within a highly regulated environment. The position is based at client's Thousand Oaks campus and follows a hybrid schedule, typically requiring two days onsite and three days remote per week, with flexibility based on project and business needs. Standard working hours are Monday through Friday, 8:00 AM to 5:00 PM Pacific Time.
Top Must Have Skills:
  • Experience working in a regulated industry, exposure to GMPs
  • Excellent verbal and written communication skills to communicate project status and risks associated with integrated timelines to leadership
  • Statistical analysis, and knowledge of Gage R&R,

Day to Day Responsibilities:
  • Collaborate with Engineers using the system to edit, develop, and run automated, experimental protocols.
  • Knowledge on Equipment and Method validation principles, equipment characterization protocols, Gauge Repeatability and Reproducibility studies
  • Assisting Engineers to successfully develop, transfer and execute processes on the integrated platforms and equipment.
  • Developing, enhancing, automating, and managing test data
  • Network with manufacturing and quality organizations internal to client
  • Ensuring all tasks and responsibilities are performed according to industry-leading scientific standards & accurately documented per SOPs
  • Monitoring technological developments in the field & evaluation of new technologies • Led the development of reference samples and test fixtures from concept to fabrication

Basic Qualifications:
Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience
Preferred Qualifications:
  • Experience working in a regulated industry, exposure to GMPs
  • Excellent verbal and written communication skills to communicate project status and risks associated with integrated timelines to leadership
  • Statistical analysis, and knowledge of Gage R&R,
  • Knowledge of force testers
  • Test method development, CAD design, Solid works, mechanical modeling
  • Manufacturing experience

Preferred Traits:
  • Passion for proactively identifying opportunities through creative data analysis and modeling
  • Intellectual curiosity with ability to learn new concepts/frameworks, algorithms, and technology rapidly as needs arise
  • Ability to manage multiple, competing priorities simultaneously, experience with MS Project, Smartsheet

Red Flags:
  • Not willing to commute to work (minimum twice a week)
  • Overqualified candidates (6+ years Pharmaceutical experience)
  • No Engineering experience
  • Job hopping (6 months or less at each place)

Interview process:
2 Stages of interview:
  • Phone screening with the hiring manager (1:1 interview with the hiring manager)
  • Panel interview if successfully passed the phone screening - Onsite

We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.