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Validation Engineer

Job in Tucson, Pima County, Arizona, 85755, USA
Listing for: The Fountain Group LLC
Contract position
Listed on 2026-07-01
Job specializations:
  • Engineering
    Quality Engineering, Manufacturing Engineer, Process Engineer
Salary/Wage Range or Industry Benchmark: 39 - 42 USD Hourly USD 39.00 42.00 HOUR
Job Description & How to Apply Below
My name is Avery, and I am a Recruiter with The Fountain Group. We are a national staffing firm and are currently seeking a Validation Engineer for a prominent client of ours. This position is located in Tucson, AZ details of the position are as follows:

Job Description:
  • Pay: $39-42hr
  • 12 Month Assignment Possibility of Extension or Conversion based on performance and budget
  • Mon – Fri
  • The position will be responsible for developing, preparing, and executing IQ, PQ, OQ, protocols and repairs for equipment/system.
  • Conducts risk assessments and develops qualification strategies for new and existing equipment/systems
  • Analyzes and interprets qualification data, ensuring accuracy, completeness, and adherence to regulatory and internal requirements.
  • Collaborates with cross-functional teams, including Process Engineering, Automation Maintenance Support, Design Transfer Operations, Manufacturing, Quality, Facilities, and Safety Health and Environment, to ensure seamless execution of qualification activities and successful achievement of qualification-related project milestones.
  • Participates in process optimization and continuous improvement initiatives to enhance quality and efficiency.
  • Ensures compliance with FDA, ISO, and other relevant regulatory guidelines, as well as adherence to internal requirements
  • Provides training and guidance to manufacturing and quality personnel on qualification processes and procedures.
  • Maintains equipment/systems qualification documentation and ensures traceability and accessibility for audits and inspections
Qualifications:
  • Bachelor’s Degree in Engineering of Life Science Required!
  • 1+ year of experience in regulated manufacturing environment
  • Strong technical writing, analytical, and problem-solving skills
  • Demonstrated experience assisting with or supporting qualification activities within the medical device, pharmaceutical, or biotechnology industry
If you are interested in hearing more about the position, please respond to this post with your resume attached or contact me at
Please forward this email to any friends or colleagues as we do offer a Referral Bonus for any candidate who is hired and still gainfully employed after 30 days.

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