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Manufacturing Validation Engineer

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Kelly Services

Petaluma, CA (In Person)

$135,200 Salary, Full-Time

Posted 1 week ago (Updated 1 week ago) • Actively hiring

Expires 5/31/2026

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Job Description

Manufacturing Validation Engineer Apply Now Applied To save a job sign in or get started
Job ID:
10159197 Posted today Back Petaluma, CA, US Engineering Bachelors Degree Full Time, Temp to Hire $60
  • 70 Experienced (Non-Manager) On-site Biotechnology/Pharmaceuticals First Shift (Day) Petaluma, CA, US $60
  • 70 Experienced (Non-Manager) Full Time, Temp to Hire Biotechnology/Pharmaceuticals On-site Engineering Bachelors Degree First Shift (Day) Apply Now Applied Job details Manufacturing Validation Engineer Kelly Engineering is seeking a hands-on Manufacturing Validation Engineer to support critical validation work for a growing life sciences manufacturer in Petaluma, CA.
Location:
Petaluma, CA Schedule:
100% Onsite |
Monday-Friday Employment Type:
Contract-to-Hire Pay Rate:
$60
  • 70/hr This is a validation-heavy engineering role supporting equipment, process, and utility qualifications in a fast-paced GMP environment.
The team is preparing for commercialization and needs someone who can independently own validation work from protocol writing through execution, deviation resolution, and final closeout. This is not a general manufacturing engineering role. This position is best suited for someone who has personally authored and executed validations in regulated manufacturing and can work independently in a startup environment with minimal handholding.
What You'll Do:
Independently author, execute, and close validation protocols for equipment, utilities, and manufacturing processes Lead IQ, OQ, and PQ activities for laboratory and manufacturing equipment Write validation protocols, final reports, deviations, work instructions, and supporting technical documentation Own validation deviations from investigation through documentation and resolution Establish process controls and technical documentation for validated systems Lead equipment qualification and commissioning activities for new and existing systems Troubleshoot validation failures and resolve technical issues during execution Support validation of laboratory and manufacturing equipment including incubators, refrigeration systems, and controlled process equipment Support qualification of facility and utility systems including water systems, piping, and related infrastructure Participate in risk assessments, FMEA, and validation impact assessments Support engineering studies and DOE activities to define process tolerances and improve validation robustness Partner cross-functionally with Quality, Manufacturing, and R D to ensure validated systems are compliant and production-ready
What You'll Need:
Bachelor's degree in Engineering or related technical discipline preferred 5-7+ years of hands-on validation experience in regulated manufacturing environments Strong experience independently authoring and executing IQ, OQ, and PQ protocols Proven experience owning validation work from protocol development through execution and final report closeout Demonstrated experience writing deviations, technical investigations, and validation documentation independently Experience supporting equipment qualification, process validation, and utility/facility validation Strong understanding of GMP and FDA-regulated environments such as pharmaceutical, biotechnology, medical device, or combination product manufacturing Working knowledge of quality systems and regulatory frameworks including
GMP, 21 CFR
Part 820, 21 CFR Part 211, and related validation standards Ability to troubleshoot technical issues during validation and make sound engineering decisions in real time Strong technical writing skills and ability to produce clear, compliant documentation Comfortable working independently in a fast-moving startup environment with evolving priorities
Ideal Background:
Validation Engineering Manufacturing Validation Process Validation Equipment Qualification GMP / FDA-regulated manufacturing Pharmaceutical, biotech, medical device, or combination product environments Candidates with primarily lean manufacturing, continuous improvement, or general production engineering backgrounds without direct validation ownership are unlikely to be a fit. 10159197 Share this job Copied url To save a job sign in or get started To apply for this job email your details to I want more jobs like this in my inbox.
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Share this job Copied url Link Copied Similar Jobs To save a job sign in or get started Sr Quality Engineer Petaluma, CA, US Full Time, Temp to Hire $60
  • 70 To save a job sign in or get started Validation Engineer Petaluma, CA, US Full Time, Temp to Hire $60
  • 70 To save a job sign in or get started Validation Engineer
  • Manufacturing Petaluma, CA, US Full Time, Temp to Hire $60
  • 70 As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources.
Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly ® Engineering? Your engineering skills are in demand, but how do you find the right fit? Easy. At Kelly Engineering, our team creates expert talent solutions to solve the world's most critical challenges. We connect you with leading organizations where you can collaborate on innovative projects, work with cutting-edge technologies and accelerate your growth. Whether you prefer the variety and flexibility of short-term projects or are looking for a long-term opportunity, we're here to guide you to the next step in your engineering career. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

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