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Pharma Validation Engineer Jobs in California (NOW HIRING)

PM Group

CQV Engineer III

Oceanside, CA · On-site

$100K - $130K/yr

We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors ... Understanding of the entire validation life cycle and change control process * Experience reviewing ...

PM Group

CQV Engineer III

Oceanside, CA · On-site

$100K - $130K/yr

We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors ... Understanding of the entire validation life cycle and change control process * Experience reviewing ...

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Pharma Validation Engineer information

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$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?

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

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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.

Product Development / Mechanical Engineer

BioQ Pharma

San Francisco, CA • On-site

Full-time

Re-posted 27 days ago

Job description

Company Description
BioQ Pharma is a privately held specialty pharmaceutical company focused on developing and commercializing ready-to-use infusible pharmaceuticals. The Company's infusion platform is intended to address some of the most pressing unmet needs in drug infusion today: cost, medication error, sterility, efficiency, and patient quality of life. BioQ Pharma's objective is to set a new standard of care in the presentation and administration of infusible pharmaceuticals via the Company's proprietary unit-dose infusion systems that can be deployed quickly and conveniently at the point of care with one touch. The Company is ISO13485 certified. BioQ Pharma's existing commercial collaborators and strategic partners include Novartis' Sandoz unit, Stada, Cipla, Lee's Pharm, Lunatus, Galen Limited, POA Pharma, Xantis Pharma, Sophos Biotech, Cooper Pharma, Lenis, Taiba, and West Pharmaceutical Services.
Job Description
Design and Develop ready-to-use infusion systems, including all aspects from early concept generation to transfer and support of production. Responsibility is primarily mechanical engineering but systems may be electromechanical and versatility and comfort with motors, electronics and software is also required.
Responsibilities will cover the full life cycle of product development and at times may include: developing and testing various product concepts based on user and market requirements, developing product requirements and specifications, designing new products, subassemblies, or components, design of injection molded parts for high volume manufacture, design for manufacturability and automation, materials research and testing, generating design output documentation, documenting and executing design verification testing and user validation testing, development and documentation of manufacturing processes, working with suppliers to ensure components meet necessary requirements and level of quality, support the transfer and ongoing production of the product at component suppliers and contract manufacturers.
Ability to travel domestically and internationally is required at times
Qualifications
  • BS or MS in Mechanical Engineering or related
  • 5 - 15 years of experience designing products from concept to manufacturing, including medical device experience
  • Strong understanding of manufacturing processes, including injection molding, machining and joining techniques
  • Solid knowledge of material properties of various plastics, metals and rubbers
  • Understanding of Design for Manufacturing (DFM) at high volumes
  • Experience working with a variety of vendors and contract manufacturers
  • Proficient in SolidWorks, drafting 2D drawings, prototyping, machining and other common shop tools
  • Basic understanding of electronics and ability to comprehend software written in C.
  • Experience designing and troubleshooting electronics, PCBs, firmware and embedded systems a plus.
  • Understanding of statistics, DOE, verification and validation activities
  • Excellent communication and documentation skills
  • Prior experience with pharmaceutical container / closure design is a plus

Additional Information
All your information will be kept confidential according to EEO guidelines.

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