Validation Engineer

    Highlights

    Assist with writing and executing Commissioning, Qualification, and Validation (CQV) protocols supporting cGMP manufacturing, fill-finish operations, and QC laboratories. Familiarity with equipment and systems such as mix tanks, autoclaves, vial/syringe fillers, HVAC systems, and aseptic processing areas.

    Numbers & Facts

    LocationMiami, FL

    Description

    Roles & Responsibilities: 
    • Execute validation studies, including performance qualifications and re-qualifications of manufacturing and laboratory equipment or processes.
    • Assist with writing and executing Commissioning, Qualification, and Validation (CQV) protocols supporting cGMP manufacturing, fill-finish operations, and QC laboratories.
    • Author acceptance reports and provide validation activity updates to project teams.
    • Support facility and utility expansions, compliance upgrades, process improvements, construction projects, and related initiatives.
    • Apply Good Documentation Practices, cGMP requirements, and current industry practices to equipment and systems validation.
    • Collaborate with Manufacturing, Quality Assurance, Engineering/Maintenance, and Quality Control teams.
    • Review change controls, work orders, document change requests, and vendor-generated validation protocol packages.
    • Update applicable SOPs following completion of validation activities.
    • Support limited multi-shift operations, training, and testing as needed.
       
    Required skills:
    • Minimum 3–5 years of experience in a sterile pharmaceutical and FDA-regulated industry.
    • Validation experience.
    • Sterile manufacturing experience.
    • Working knowledge of Microsoft Office applications.
    • Knowledge of cGMP requirements, Good Documentation Practices, and validation of manufacturing and laboratory equipment or processes.
    • Strong technical writing, communication, organization, and cross-functional collaboration skills.
    • Familiarity with equipment and systems such as mix tanks, autoclaves, vial/syringe fillers, HVAC systems, and aseptic processing areas.
      Education 
    • Associate of Science degree in a technical or scientific discipline required, or three years of related experience in lieu of a degree.
    • Bachelor of Science degree desired.
       
     

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