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Katalyst HealthCares & Life Sciences

Senior Quality Validation Lead

Katalyst HealthCares & Life Sciences, Boston

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  • Understands regulations pertaining to the implementation and use of computerized systems in all GxP areas.
  • Participates in system implementation project teams to provide guidance on System Lifecycle activities and validation strategy to be followed using a risk-based approach based on GAMP 5.
  • Reviews and approves system lifecycle deliverables for new and modifications to computerized systems used in the GxP areas.
  • Consults with QISM team members and relevant internal stakeholders to identify / define high risk areas with the intent on focusing on patient safety, product quality and data integrity.
  • Identifies and escalates areas of risk or non-compliance to manager / leadership team.
  • Participates in performing Periodic Review activities of Computerized Systems.
  • Provide support to regulatory inspection preparedness activities as needed.
  • Experience performing Infrastructure Qualification activities.
Responsibilities
  • Understands regulations pertaining to the implementation and use of computerized systems in all GxP areas.
  • Participates in system implementation project teams to provide guidance on System Lifecycle activities and validation strategy to be followed using a risk-based approach based on GAMP 5.
  • Reviews and approves system lifecycle deliverables for new and modifications to computerized systems used in the GxP areas.
  • Consults with QISM team members and relevant internal stakeholders to identify / define high risk areas with the intent on focusing on patient safety, product quality and data integrity.
  • Identifies and escalates areas of risk or non-compliance to manager / leadership team.
  • Participates in performing Periodic Review activities of Computerized Systems.
  • Provide support to regulatory inspection preparedness activities as needed.
  • Experience performing Infrastructure Qualification activities.
Requirements:
  • Bachelor's degree and relevant GxP work experience.
  • Proficiency in using Microsoft Office applications.
  • 8-10 experience performing validation activities.
  • Proficiency with regulations related to FDA / MHRA regulations.
  • Use of computerized quality management systems.
  • Experience with validation of Enterprise / Lab Computerized Systems.
  • Quality metrics, dashboards, analysis and improvement programs.
  • Knowledge of GAMP and Agile validation lifecycle and methodologies.

Seniority level

  • Seniority level

    Mid-Senior level

Employment type

  • Employment type

    Contract

Job function

  • Job function

    Quality Assurance
  • Industries

    Pharmaceutical Manufacturing

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