Senior Aseptic Processing & Contamination Control Consultant (FT, Contract)

Workforce Genetics

  • Baltimore, Maryland
  • 30+ days ago

    Highlights

    You will facilitate risk assessment workshops and guide the execution of FMEA models across 100+ high-risk manual interventions to identify contamination mechanisms and drive risk reduction strategies via the eliminate-replace-reduce-control engineering hierarchy in support of CAPA-102537, CAPA-102539, and ICP-100445. The company provides sterile injectables and offers clinical and commercial non-viral aseptic fill/finish services for vials and pre-filled syringes on four fill lines, in addition to lyophilization, terminal sterilization, analytical, stability, packaging and serialization, and additional support services.

    Numbers & Facts

    LocationBaltimore, Maryland

    Description

    Our client is hiring a Senior Aseptic Processing & Contamination Control Consultant to provide technical leadership for a 2-month (approx. 12-week) full-time contract project addressing FDA 483 audit findings. In this role, you will perform a thorough review and risk assessment of legacy aseptic fill-finish processes (focusing on non-isolator, manual assembly environments and first air challenges). You will facilitate risk assessment workshops and guide the execution of FMEA models across 100+ high-risk manual interventions to identify contamination mechanisms and drive risk reduction strategies via the eliminate-replace-reduce-control engineering hierarchy in support of CAPA-102537, CAPA-102539, and ICP-100445.


    Experience:

    • 15+ years of sterile manufacturing and legacy aseptic systems experience (manual assembly, open RABS/laminar flow environments)
    • Deep aseptic processing expertise and FMEA risk profile model execution
    • First air principles specialist
    • Contamination control expert
    • Strong documentation skills
    • Aseptic risk assessment workshop facilitation
    • Application of eliminate-replace-reduce-control risk reduction hierarchy


    Day-to-Day Responsibilities:

    • Facilitate risk assessment workshops to map detailed step-by-step process executions (e.g., ~25-step manual interventions) in legacy, non-isolator aseptic systems.
    • Identify specific contamination mechanisms and first air disruption risks across legacy manual assembly environments.
    • Perform Failure Mode and Effects Analysis (FMEA) to calculate Risk Priority Numbers (RPN) and quantify risk drivers for high-risk interventions.
    • Drive risk reduction strategies using the eliminate-replace-reduce-control engineering hierarchy to establish interim and long-term mitigations.


    The company provides sterile injectables and offers clinical and commercial non-viral aseptic fill/finish services for vials and pre-filled syringes on four fill lines, in addition to lyophilization, terminal sterilization, analytical, stability, packaging and serialization, and additional support services.

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