Ocular Health R&D Engineer

BioPharma Consulting JAD Group

  • Fort Worth, TX
  • 5 days ago

    Highlights

    Supports in the designs and development of a wide variety of packaging and/or device used for the protection, display, handling, and delivery of ophthalmic pharma products. Data Analysis & Documentation o Capable of analyzing test results, identifying trends or failures, and summarizing findings clearly.

    Numbers & Facts

    LocationFort Worth, TX

    Description

    • Hands-on and Technical Testing Competency o Ability to perform standardized tests per SOP and test methods.
    • Understands protocols, data collection, and proper use of lab equipment. o Focused on accuracy, repeatability, and compliance o Perform equipment validation (IQ/OQ, etc.)
    • Data Analysis & Documentation o Capable of analyzing test results, identifying trends or failures, and summarizing findings clearly.
    • Writes structured test protocol, reports and maintains documentation aligned with quality and regulatory requirements
    • Problem Solving & Root Cause Analysis
    • Can identify potential issues in performance and support investigations (e.g., basic CAPA input, troubleshooting test failures).
    • Collaborates with engineers to improve designs, performance or test methods based on results.
    • Supports in the designs and development of a wide variety of packaging and/or device used for the protection, display, handling, and delivery of ophthalmic pharma products.
    • Performs assigned tasks under general supervision in support of approved projects.
    • Executes engineering studies, conduct testing and data analysis under direction of senior OH team members. Receives technical guidance from senior OH staff on the design of experiments.
    • Applies general technical skills to complete assigned work and solves routine problems of limited scope.
    • Thoroughly and clearly documents experiments in laboratory notebook and assists in preparation of technical documents.
    • Drafts protocol and reports to document related activities
    • Drafts and routes standard operating procedures as required
    • Drives effective actions for compliance within the agreed timelines
    • Ensures continual quality system compliance by adherence to established and evolving QS requirements.
    • Communicates and collaborates with colleagues and with supervisors.
    • General use, set-up and upkeep of laboratory, including equipment/instrumentation

    Requirements

    • Bachelor’s Degree or Equivalent + 2 years of directly related experience (or high school +8 yrs; Assoc.+6yrs; M.S.+0 yrs), Mechanical Engineering major is desired
    • Years of experience: 2+ years of directly related experience with a Bachelor's degree, or +0 years of experience with a Master's degree
    • The ability fluently read, write and communicate in English.
    • Hands-on Technical Testing Competency
    • Equipment Validation Experience (IQ/OQ)
    • Technical Documentation, Problem Solving and Root Cause Analysis

    Benefits

    • Schedule: 40 hours per week, Monday - Friday.
    • Contract position with posible extension

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