Visiting to DS manufacturing and warehouse facility to ensure that activities are being carried out by following GMP requirements, Regulatory requirement and as per approved procedures.
Line clearance for the process operation during manufacturing activity (Drug Substance).
Preparation and review the Risk Assessment and Mitigation Plan.
Ensure that process and cleaning validation activities are being carried out by following approved protocols.
Review of master document like study protocol, BPR, MFR etc.
Review of executed Batch Processing Records for Batch Release.
Review of Batch Dispatch Record and verification of dispatch activities in warehouse.
Preparation and review of Quality System SOPs & documents.
Review of SOPs as per GMP requirements for all departments.
Work Experience 0 to 3 Years Education Masters in Biotechnology or Biotechnology Competencies 1. Strategic Agility 2. Innovation & Creativity 3. Customer Centricity
Beware of fraud agents! do not pay money to get a job
MNCJobsIndia.com will not be responsible for any payment made to a third-party. All Terms of Use are applicable.