Validation Engineer jobs in California

Validation Engineer prepares all protocols and reports for validation work. Coordinates all validation activities by constant communication with affected departments and personnel; oversees and reviews validation area processes and procedures. Being a Validation Engineer may require a bachelor's degree. Typically reports to a manager or head of a unit/department. The Validation Engineer works on projects/matters of limited complexity in a support role. Work is closely managed. To be a Validation Engineer typically requires 0-2 years of related experience. (Copyright 2024 Salary.com)

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MV01-011924 Engineer (California)
  • Validation & Engineering Group, Inc.
  • Thousand Oaks, CA FULL_TIME
  • Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

    We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

    • Engineer

    This engineering position supports manufacturing activities associated with cGMP equipment and facilities. The engineer works in partnership with the automation, maintenance, project management, corporate engineering, and manufacturing to develop and oversee the operation and reliability of equipment while driving safety and quality compliance. The engineer will support the department and capital projects and provide data to support business cases and long-term strategy.

    The Engineer role will provide direct engineering technical support as follows:

    • Model leadership behaviors and positive values to create a positive working environment.
    • Be individually accountable for the consistent equipment performance
    • Be accountable for assigned deliverables on key capital projects
    • Suggest design modifications to address risks and design in quality and safety.
    • Provide oversight for verification deliverables developed by outsourced/contract verification staff.
    • Act as a liaison between Engineering and Quality Assurance during project planning, execution, and closeout
    • Ensure that validation protocols are executed and documented in accordance with cGMP good documentation and safety compliant practices.
    • Ensure safety during commissioning, validation, maintenance, and manufacturing activities

    Related Activities

    • Participate or lead, when required, multidisciplinary site teams, e.g. Cross Functional Team, Root Cause Analysis lead.
    • Support Lean Transformation and Excellence in Operations process improvement by leading, supporting, and documenting improvement opportunities to reduce cost, improve safety/quality, or improve speed.
    • Provide ad hoc technical support and guidance for manufacturing and maintenance
    • Provide coaching and guidance to project teams and engineers using risk-based approaches
    • Defend the equipment-specific calibration, maintenance, & validation as required during regulatory inspections
    • Participate in internal audits and assess in conjunction with quality assurance
    • Assist in developing and maintaining business metric performance

    Preferred Qualifications / Skills / Experience

    • Bachelor's degree in engineering.
    • 2 years of relevant work experience.
    • Direct experience with regulated environments (FDA, OSHA, EPA, etc.)
    • Working knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech production processes, clean utilities, facilities, instruments, and equipment
    • Experience implementing risk-based verification on major GMP process equipment / automation projects, including validation protocol development and execution.
    • Experience with combination product / medical device quality systems verification.
    • Process equipment knowledge – basic principles of cell culture, fermentation, purification, filling
    • Process automation knowledge – fundamental understanding of automation infrastructure
    • Knowledge of Delta V, Rockwell, and Plant Information Systems is a plus
    • Strong communication and technical writing skills.
    • Strengths in facilitation and collaboration / networking
    • Experience in developing SOPs and delivering training
    • Individual must be a team player prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making
    • Basic understanding of process improvement methodologies to mature and improve business performance (examples: PDCA, LEAN, Six Sigma, etc.)
  • 6 Days Ago

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MV01-011924 Engineer (California)
  • Validation & Engineering Group
  • Newbury, CA FULL_TIME
  • Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following...
  • Just Posted

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Welder fabricator
  • The Engineer
  • Brentwood, CA FULL_TIME
  • The RoleWe are looking for a fabricator / welder who will work both in our workshop, based in West Horndon, Essex and onsite. Key Responsibilities : Predominantly welding - gaining and maintaining the...
  • 25 Days Ago

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Validation Engineer
  • PSC Biotech
  • Pomona, CA FULL_TIME
  • PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applica...
  • 2 Days Ago

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Validation Engineer
  • Phillips-Medisize
  • Costa Mesa, CA FULL_TIME
  • Your JobPhillips-Medisize, a Molex Company is an end-to-end provider of innovation, development, and manufacturing solutions to the pharmaceutical, diagnostics, and medical device industries. Our Glob...
  • 2 Days Ago

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Validation Engineer
  • Katalyst HealthCares & Life Sciences
  • La Verne, CA CONTRACTOR
  • ResponsibilitiesLead the commissioning and qualification activities for aseptic fill manufacturing equipment, including vial washers, depyrogenation tunnels, isolators, sterile fillers, and cappers.De...
  • 5 Days Ago

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Process Validation Engineer (Contract)
  • a Biopharmaceutical company based out PA
  • Philadelphia, PA
  • Process Validation Engineer (Contract) RESPONSIBILITIES Overseeing and reviewing design and construction work related to...
  • 6/11/2024 12:00:00 AM

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Process Validation Engineer
  • Katalyst HealthCares and Life Sciences
  • Austin, TX
  • Evaluate validation of the equipment, software and processes used in development and production of medical products ensu...
  • 6/11/2024 12:00:00 AM

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Validation Engineer
  • Hays
  • Auburn Hills, MI
  • Validation Engineer – Contract – Auburn hills, MI – $30.00-$35.00/hr The final salary or hourly wage, as applicable, pai...
  • 6/11/2024 12:00:00 AM

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Validation Engineer
  • Merck & Co., Inc.
  • Lansdale, PA
  • Qualifications: Associate’s degree or higher preferred with 1-2 years of experience or 4-5 years working experience in m...
  • 6/11/2024 12:00:00 AM

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Process Validation Engineer
  • Technical Source
  • Technical Source is currently in search of a Process Validation Engineer for our pharmaceutical manufacturing client in ...
  • 6/10/2024 12:00:00 AM

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Validation Engineer
  • ACL Digital
  • San Diego, CA
  • Job Title: Systems Test Engineer (Silicon Validation) Location: San Diego, CA (Onsite) Duration: Contract Project Job De...
  • 6/10/2024 12:00:00 AM

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Process Validation engineer (SME)
  • AR Validation Services
  • Boston, MA
  • Project Description: We are looking for a process validation engineer with experience in an aseptic/sterile environment....
  • 6/8/2024 12:00:00 AM

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Process Validation Engineer (Medical Devices)
  • Katalyst HealthCares and Life Sciences
  • Austin, TX
  • Evaluate validation of the equipment, software and processes used in development and production of medical ! products en...
  • 6/7/2024 12:00:00 AM

California is a state in the Pacific Region of the United States. With 39.6 million residents, California is the most populous U.S. state and the third-largest by area. The state capital is Sacramento. The Greater Los Angeles Area and the San Francisco Bay Area are the nation's second and fifth most populous urban regions, with 18.7 million and 9.7 million residents respectively. Los Angeles is California's most populous city, and the country's second most populous, after New York City. California also has the nation's most populous county, Los Angeles County, and its largest county by area, S...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Validation Engineer jobs
$61,880 to $82,658

Validation Engineer in Muskegon, MI
As the Process Validation Engineer you will perform process validation activities to ensure cGMP requirements are met with regards to the IQ, OQ and PQs.
February 08, 2020
Validation Engineer in Ogden, UT
Knowledge of system validation “life-cycle” concept.
February 17, 2020
Validation Engineer in Baton Rouge, LA
There are validation engineer job opportunities across the entire industry including pharmaceutical, biotechnology and medical devices companies.
December 18, 2019