Demo

CQV Technical Lead

Katalyst HealthCares & Life Sciences
Indianapolis, IN Contractor
POSTED ON 2/16/2025
AVAILABLE BEFORE 3/15/2025
Responsibilities

  • Coordination and maintenance of CQV.
  • Review of Protocols.
  • Execution of approved protocols including generating/closure of all protocol deficiencies (deviation).
  • Generation of maintenance plans within CMMS.
  • Generation of Qualification summary report i.e. Summary Report, Trace Matrix.
  • Generation of handover release form.

Requirements:

  • Document revision and Approval Follow-up for URS, TQPAS.
  • Require Onsite resource assigned at the site.
  • Trained on GMP curricula to support CQV activities.
  • Create New Documents and Support review and approval of the following documents.
  • Execution of approved protocols including generating/closure of all protocol deficiencies.

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