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Pharma Validation Engineer Jobs in California (NOW HIRING)

Syntricate Technologies

AWS Data Engineer Lead

Alameda, CA · On-site

$132K - $159K/yr

... Pharma & Commercial Operations Domain Knowledge is must Preferred : • AWS Certified Data ... Company : Syntricate Technologies offers quality assurance, validation, regulatory, business ...

Mithrl

Forward Deployed Engineer

San Francisco, CA · On-site

$150K - $200K/yr

Trusted by leading biotechs and big pharma across three continents * Driving real breakthroughs ... Validate deployed environments through functional, performance, and scientific smoke tests

Mithrl

Forward Deployed Engineer

San Francisco, CA · On-site

$150K - $200K/yr

Trusted by leading biotechs and big pharma across three continents * Driving real breakthroughs ... Validate deployed environments through functional, performance, and scientific smoke tests

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All JobsPharma Validation Engineer JobsPharma Validation Engineer Jobs in California

Pharma Validation Engineer information

See California salary details

$22

$51

$77

How much do pharma validation engineer jobs pay per hour?

As of Sep 2, 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?

Cities in California with the most Pharma Validation Engineer job openings:

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.

Manufacturing Engineer

Stark Pharma Solutions Inc

Santa Rosa, CA • On-site

$79K - $102K/yr

Contractor

Re-posted 19 days ago

Job description

About the Company


Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.

Manufacturing Engineer

Role:
Seeking a Mechanical Engineer with strong manufacturing and training experience to support process development, standardization, and workforce training within a regulated medical device environment. The role focuses on developing process flows, assembling and deploying TWI (Training Within Industry) programs, and creating a process dictionary to support consistent execution across the product line.

Key Responsibilities:

  • Develop, document, and maintain detailed manufacturing process flows for medical device product lines.
  • Assemble, customize, and deploy TWI training materials to support operator training and standard work.
  • Create and maintain a process dictionary to standardize terminology, steps, and training content across manufacturing operations.
  • Support process mapping and optimization across the full product lifecycle, from pilot builds through full production.
  • Collaborate cross-functionally with Manufacturing, Quality, R&D, and Operations to ensure processes meet design and regulatory requirements.
  • Ensure all processes, documentation, and training materials comply with FDA and ISO 13485 requirements.
  • Support continuous improvement initiatives focused on efficiency, quality, and repeatability.
  • Assist with process validation support as needed.

Required:

  • Bachelor's degree in Mechanical Engineering.
  • 5+ years of experience in medical device manufacturing or a regulated environment.
  • Hands-on experience developing and implementing TWI (Training Within Industry) programs.
  • Strong experience creating process flows, work instructions, and training documentation.
  • Experience establishing and maintaining process dictionaries or standardized manufacturing documentation.
  • Solid understanding of medical device manufacturing processes and regulatory expectations (FDA, ISO 13485).