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Remote Validation Jobs in California (NOW HIRING)

Danaher

Senior Engineer, Process Validation

Sunnyvale, CA · On-site +1

$100K - $130K/yr

This position reports to the Process Validation Manager and is part of the Technical Operations Department located in Fargo, ND and will be fully remote. In this role, you will have the opportunity ...

Danaher

Senior Engineer, Process Validation

Sunnyvale, CA · On-site +1

$100K - $130K/yr

This position reports to the Process Validation Manager and is part of the Technical Operations Department located in Fargo, ND and will be fully remote. In this role, you will have the opportunity ...

Intersect

Microgrid Validation Lead

San Francisco, CA · On-site +1

Microgrid Validation Lead About This Role As part of Intersect's Microgrid Engineering team, you'll lead the development of the validation strategy, infrastructure, and testing methodologies that ...

General Motors

Senior ML Validation Engineer

Sunnyvale, CA · On-site +1

$144K - $261K/yr

The Senior ML Validation Research Engineer will lead applied machine learning research focused on improving verification and validation of ML components used in robotics and autonomous driving ...

YO AI Labs

Biostatistician Expert - Remote

San Jose, CA · Remote

$60 - $70/hr

Remote Job Type: Contractor Pay: $60-$65/hour Job Overview We are looking for an experienced ... Analyze and validate clinical trial data. * Review and interpret Statistical Analysis Plans (SAPs)

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How much do remote validation jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for remote 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 remote validation?

A Remote Validation job involves ensuring that systems, software, or processes meet specified requirements and function correctly, typically in regulated industries like pharmaceuticals, healthcare, or manufacturing. Professionals in this role conduct tests, analyze data, and document compliance, all while working remotely. They may validate software applications, equipment, or processes to meet regulatory standards such as FDA, ISO, or GMP guidelines. Strong attention to detail, knowledge of validation protocols, and proficiency with industry regulations are essential for success in this role.

What are the key skills and qualifications needed to thrive in remote validation?

To thrive in Remote Validation, you need a solid background in quality assurance, process validation, and regulatory compliance, often supported by a degree in engineering, life sciences, or a related field. Familiarity with validation protocols, statistical analysis software, and documentation systems like TrackWise is highly valuable, along with certifications such as Six Sigma or ASQ. Excellent attention to detail, strong communication skills, and the ability to work independently are critical soft skills. These competencies ensure rigorous validation processes, effective remote collaboration, and compliance with industry standards.

What are common challenges faced in a remote validation role and how are they addressed?

One of the most common challenges in a Remote Validation position is ensuring thorough communication and documentation when coordinating with on-site teams and cross-functional colleagues. To overcome this, professionals in this role rely heavily on detailed reporting, frequent virtual meetings, and collaborative project management tools to maintain alignment and transparency. Adapting validation strategies to a remote environment also requires a strong understanding of digital validation tools and best practices for remote audits. Regular training and clear standard operating procedures can help keep validation processes efficient and compliant, even when working off-site.

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

The most popular types of Validation jobs in California are:

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

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

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

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

What cities in California are hiring for Remote Validation jobs?

Cities in California with the most Remote Validation job openings:

Remote Validation jobs near you
Infographic showing various Remote Validation job openings in California as of August 2026, with employment types broken down into 91% Full Time, 6% Part Time, and 3% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $106,736 per year, or $51.3 per hour.

CQV Validation Engineer, Biotech GMP Equipment - Remote (JP15497)

3 Key Consulting

Thousand Oaks, CA • Remote

$46 - $52/hr

Full-time

Re-posted 20 days ago

Key responsibilities

  • Execute periodic reviews of GMP equipment according to approved procedures and schedules.

  • Evaluate equipment records to verify continued fitness for intended use.

  • Generate and/or revise periodic review reports.

Job description

Job Title: CQV Validation Engineer, Biotech GMP Equipment – Remote (JP15497)
Location: Thousand Oaks, CA. 91320
Employment Type: Contract
Business Unit: Engineering Systems
Duration: 12+ months with likely extensions and/or conversion to permanent
Posting Date: 06/16/2026
Pay Rate: $46 - $52/hour W2 with benefits
Notes: Fully Remote.
3 Key Consulting is hiring a C&Q Validation Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Primarily responsible for planning, coordinating, executing, and documenting periodic reviews of GMP equipment to ensure continued state of validation, compliance with regulatory requirements, and suitability for intended use.  The role partners with Engineering, Manufacturing, Quality Assurance, Validation, and Maintenance teams to assess equipment performance, maintenance history, calibration status, deviations, change controls, and overall lifecycle management.
Key skills and requirements:
• Demonstrable experience in a pharmaceutical, biotech, or life science organization in a C&Q/CQV/validation maintenance role.
• Knowledge of cGMP commissioning/qualification/validation practices.
• Familiarity with biotech/pharmaceutical manufacturing equipment.
• Familiarity with Kneat Gx Platform or other digital C&Q systems.
• Experience working with cross-functional stakeholders.
• Knowledge of quality assurance principles including deviations and change control systems.
• Effective communication skills, both verbal and written.
• Able to think analytically with the ability to resolve issues.
• Able to manage own time efficiently.
Position could be extended to up to 3 years
Why is the Position Open?
Planned Project.
Top Must Have Skills:
Experience in commissioning/qualification/validation, experience in a GMP environment, knowledge of biotech/pharmaceutical manufacturing equipment
Day to Day Responsibilities:
• Execute periodic reviews of GMP equipment according to approved procedures and schedules. Assess
 equipment records including work orders, deviations, and change control records.
• Evaluate equipment records to verify continued fitness for intended use.
• Generate and/or revise periodic review reports.
• Collaborate with Manufacturing, System Owners, Validation, and Quality teams as needed.
• Schedule and lead review meetings as needed to resolve issues.
• Ensure reviews are completed within established timelines and regulatory expectations.
• Maintain periodic review trackers and metrics.
• Identify opportunities to improve the equipment periodic review process.
• Other duties may be assigned to this role.
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
Employee Value Proposition:
Industry experience.
Red Flags:
Short tenures at previous jobs (<2 years)
No experience in commissioning/qualification/validation
Interview process:
1-2 Stages of interview | Video interview (Teams)
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.