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Pharma Validation Engineer Jobs in California (NOW HIRING)

JSat Automation

Validation Engineer

Glendale, CA · On-site

JSat Automation is hiring a full time Validation Engineer with Pharma Industry experience. The Validation Engineer will be responsible for the following. * Develop, approve, and execute process ...

Kite Pharma

Sr Validation Engineer I

Oceanside, CA · On-site

We are seeking a highly effective Senior Validation Engineer responsible for planning, execution ... Master's degree with 5+yearsof experience in validation in a biotech/pharma industry * Experience ...

Katalyst CRO

CSV Engineer

Redwood City, CA · On-site

... regulated pharma environments. Responsibilities : • Validating Veeva platforms within a ... CSV Engineer • Ensuring compliance with validation and regulatory standards Qualifications

Spyglass Pharma

Sr. Engineer, R&D

Aliso Viejo, CA · On-site

$110K - $151K/yr

At SpyGlass Pharma (NASDAQ: SGP), we are focused on improving and preserving the vision of patients ... Lead the design, planning, and execution of complex experiments and validation studies to support ...

Spyglass Pharma

Sr. Engineer, R&D

Irvine, CA · On-site

$120K - $140K/yr

At SpyGlass Pharma (NASDAQ: SGP), we are focused on improving and preserving the vision of patients ... Lead the design, planning, and execution of complex experiments and validation studies to support ...

Spyglass Pharma

Sr. Engineer, R&D

Irvine, CA · On-site

$111K - $153K/yr

At SpyGlass Pharma (NASDAQ: SGP), we are focused on improving and preserving the vision of patients ... Lead the design, planning, and execution of complex experiments and validation studies to support ...

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Pharma Validation Engineer information

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$51

$77

How much do pharma validation engineer jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for pharma validation engineer 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 pharma validation engineer?

A Pharma Validation Engineer ensures that manufacturing processes, equipment, and systems in the pharmaceutical industry comply with regulatory standards such as FDA, GMP, and ISO. They develop validation protocols, conduct tests, analyze data, and generate reports to ensure consistent product quality and safety. Their role is critical in minimizing risks, maintaining compliance, and supporting regulatory audits.

What does a pharma validation engineer do?

A typical day for a Pharma Validation Engineer involves developing and executing validation protocols for manufacturing equipment, laboratory instruments, or processes, ensuring they meet all regulatory and quality standards. You might collaborate closely with QA teams, production staff, and external vendors to troubleshoot issues, review data, and document results for compliance audits. Preparing detailed reports, participating in cross-functional meetings, and staying updated with current regulatory changes are also common responsibilities. This dynamic environment offers opportunities to work on diverse projects and continually expand your technical expertise while supporting product safety and efficacy.

What skills and qualifications are needed to be a pharma validation engineer?

To thrive as a Pharma Validation Engineer, you need a solid background in engineering or life sciences, with expertise in validation protocols, regulatory compliance (such as FDA or EMA guidelines), and Good Manufacturing Practices (GMP). Experience with validation software (like ValGenesis or MasterControl), statistical analysis tools, and relevant certifications (such as Six Sigma or ISPE) is highly valued. Strong attention to detail, project management abilities, and effective communication skills are crucial for this role. These competencies ensure validation activities meet strict regulatory standards, support product quality, and facilitate seamless cross-functional collaboration in the pharmaceutical industry.

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

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

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

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

What cities in California are hiring for Pharma Validation Engineer jobs?

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Pharma Validation Engineer jobs near you
Infographic showing various Pharma Validation Engineer job openings in California as of August 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $106,736 per year, or $51.3 per hour.

Validation Engineer

JSat Automation

Glendale, CA • On-site

Full-time

Medical, Retirement, PTO

Re-posted 21 days ago

Job description


JSat Automation is hiring a full time Validation Engineer with Pharma Industry experience.
The Validation Engineer will be responsible for the following.
  • Develop, approve, and execute process validation studies and protocols for cell and gene therapy manufacturing.
  • Design and develop manufacturing control systems in support of process operations.
  • Interact with client personnel to identify and analyze continuous improvement through automation upgrades.
  • Develop validation documents per FDA cGMP and GAMP standards, functional specifications, design specifications and requirements trace matrices.
  • Design, program, test and validate process control automation systems.
  • Prepare and execute validation protocols (AIQ, IQ, OQ) for 21 CFR Part 11 compliance per FDA requirements
  • Manage, document, and implement these upgrades through changes control procedures.
  • Execute capital projects including but not limited to:
  • Control system software development
  • Control system hardware design
  • Network design
  • MES system implementation
  • Recipe management
  • User requirement specification development
  • Process equipment installations.
  • SOP development and training on Automation Systems.
  • Troubleshoot, analyze, and resolve field control system issues.
  • Develop, review, and / or execute automation qualification and validation protocols.
  • Design, develop, and implement technical solutions by establishing integration strategies, configuring and programming PLCs, DCSs as well as design, build, install and integrate automation control system hardware, panels and field devices.

Requirements
  • Chemical engineers preferred, with a minimum of three (3) years relevant experience.
  • Experience in Control Systems (Emerson DeltaV, Allen Bradley, Foxboro, Siemens, Honeywell). Experience with SCADA, MES, and database systems, or computer system validation are considered a plus.

Benefits
Health, PTO, Retirement Plan

Apply