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Validation Engineer

Job in Tucson, Pima County, Arizona, 85718, USA
Listing for: SQA Solution
Full Time position
Listed on 2026-06-26
Job specializations:
  • Engineering
    Quality Engineering, Biomedical Engineer, Manufacturing Engineer, Process Engineer
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly USD 70000.00 90000.00 YEAR
Job Description & How to Apply Below

Please note that at this time we are unable to sponsor employment authorization (both new and transfer)

A global biotechnology leader is seeking a proactive Validation Engineer with 1-3 years of experience in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA) to ensure compliance and drive operational integrity.

Responsibilities
  • Develops, prepares, and executes IQ, OQ, and PQ protocols and reports for equipment/systems.
  • 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 (SHE), 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.
  • Other duties as assigned by management.
Qualifications
  • Bachelor's Degree in Engineering or Life Science.
  • 1-3 years of experience in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA). Focus:
    Equipment Qualification.
  • Strong technical writing, analytical, and problem-solving skills.
  • Demonstrated experience assisting with or supporting qualification activities within the medical device, pharmaceutical, or biotechnology industry is required.

We are an Equal Opportunity employer and welcome talent across all aspects of background, orientation, origin, and identity in an inclusive and non-discriminatory way. Applicants receive consideration without bias and based on the relevant qualifications, talents, skills, experiences, and business needs

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