Senior Validation Engineer

Katalyst Healthcares & Life Sciences

  • Silver Springs, MD
  • 30+ days ago
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    Skills

    • Asset Managementunmatched
    • Calibrationunmatched
    • Documentationunmatched
    • Equipment Maintenance/Repairunmatched
    • Equipment Validationunmatched
    • Facilities Managementunmatched
    • Medical Equipmentunmatched
    • On Site Supportunmatched
    • Operational Auditunmatched
    • Process Improvementunmatched
    • Quality Assuranceunmatched
    • Quality Assurance Methodologyunmatched
    • Support Documentationunmatched
    • System Lifecycleunmatched
    • Systems Administration/Managementunmatched
    • Traceabilityunmatched
    • Validation Documentationunmatched
    • Validation Planunmatched

    Description

    Requirements:
    • Minimum five (5) years of experience specific/applicable to the below requirements.
    • Support the completion of the following LBE Projects:
    • Equipment/systems lifecycle management support for the commercial launch of Medical Device.
    • Transition activities supporting new systems/equipment/components for perfusion services/devices used at facilities, facility change activities.
    1. Develop, revise, review and execute validation documents in support of equipment lifecycles. Documents include but are not limited to:
      1. User Requirement Specifications,
      2. Validation Determination Assessments,
      3. Standards Qualification Forms,
      4. Installation/Operational/Performance Qualifications,
      5. Requirements Traceability Matrix,
      6. Summary/Final Reports
    2. Serve as on-site support/contact for:
      1. Validation contractors:
    • Meet with contractors, perform pre-review of validation documents to support efficient review/approval by QA.
    • Lead the effort for protocol discrepancy related documentation and assist contractors in investigations related to protocol deviations.
      1. Operations:
    • Collaborate with operations team to assess and update validation documents (VDAs, URS, Specifications, Trace documents) in support of user needs, process changes, and business improvements, and commercialization efforts.
    • Support validation/qualification efforts for facility expansion.
      1. Quality Assurance:
    • Maintaining validated state of equipment. Ensure equipment parameters are maintained, especially after calibration/maintenance events.
    • Ensuring efficient and coordinated executions of validation events. Work with QA/Clinical team to minimize disruption to clinical operations.
    iii. Execute validation protocols.
    iv. Perform/support periodic review cycles for LBE equipment.
    v. Assist with device related installation activities.
    • Act as a validation/equipment point of contact for Facility Managers and Quality Assurance.
    • Lead equipment/asset management process (for QA group) utilizing the Blue Mountain RAM system (electronic Asset/Equipment Manager).
    • Collaborate with on-site contractors/operations team to document calibration/PM work and electronically manage equipment assets.
    • Ensure RAM system, facility equipment, and equipment identification are aligned to support equipment control/management throughout the lifecycle.

    Numbers & Facts

    LocationSilver Springs, MD

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