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Validation Engineer

Job in San Jose, Santa Clara County, California, 95199, USA
Listing for: BEPC Inc. - Business Excellence Professional Consulting
Contract position
Listed on 2025-12-13
Job specializations:
  • Engineering
    Biomedical Engineer, Validation Engineer, Pharma Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 57 - 62 USD Hourly USD 57.00 62.00 HOUR
Job Description & How to Apply Below
Position: Validation Engineer I

Validation Engineer I

Benefits: Medical, Dental, Vision, and Life Insurance

Pay Rate: $57-$62 per hour (Paid Weekly)

Term: 6-months contract with possible extensions

Requirements: Bachelor’s degree in engineering, Science, or a related technical field, 1+ year of validation experience within a medical device, pharmaceutical, biotechnology, or other regulated industry.

NO CORP-TO-CORP CANDIDATES WILL BE CONSIDERED

BEPC does not accept C2C, C2H, or W2 referral applications.

Duties & Responsibilities
  • Develop equipment and fixture matrices with defined qualification requirements in accordance with medical device regulations and client standards.
  • Create detailed, compliant Installation Qualification (IQ) and Operational Qualification (OQ) protocols for manufacturing and laboratory equipment.
  • Execute IQ/OQ protocols, ensuring accurate data collection, documentation integrity, and adherence to regulatory and client requirements.
  • Write and issue validation summary reports following successful protocol execution.
  • Provide technical support for the development and implementation of Standard Operating Procedures (SOPs) related to newly qualified equipment and fixtures.
  • Perform troubleshooting, root cause analysis, and implement corrective actions to resolve validation and compliance issues.
  • Ensure validation activities comply with FDA regulations, ISO 13485, GMP, GAMP, and internal policies.
  • Manage multiple validation projects simultaneously, including documentation, scheduling, and communication with internal and client stakeholders.
  • Own and execute the full equipment/fixture validation lifecycle, from documentation development through testing and final reporting.
Education & Experience Requirements
  • Bachelor’s degree in engineering, Science, or a related technical field.
  • 1+ year of validation experience within a medical device, pharmaceutical, biotechnology, or other regulated industry.
  • Working knowledge of:
    • ISO 13485
    • FDA 21 CFR Part 820
    • 21 CFR Part 11
    • GMP
    • GAMP
  • Must be able to speak, read, comprehend, and write English.
Seniority level

Associate

Employment type

Contract

Job function

Medical Equipment Manufacturing

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