Job SummaryResponsible for Vendor Qualification/disqualification for Pharma division and other activities including GMP assessment and compliance as per regulatory requirements.ResponsibilitiesVendor qualification, requalification and disqualification of raw materials and packaging materials vendors as per the company's standard procedure including compliance to quality system.To Schedule/Plan vendor audit of APIs vendors and Primary Packaging vendorsTo conduct audit (virtual & site audit) of Raw materials and Packaging materials vendors as per the schedule.Responsible for review and disposition discrepancy for raw material and packaging.Perform vendor evaluation through the risk assessment for APIs, Excipients and Primary Packaging Materials vendors.Review and approval of specification and standard test procedure of raw materials and packaging material w.r.t. vendor.Creation of Q-info in system for raw material (APIs & Excipients) and packaging materials.To conduct the internal quality audit to review the implementation of systems as per the design and to ensure the cGMP compliance.To coordinate with customers as GSK and Bayer for day to day activity and implement the quality management system whatever required.Preparation, review and approval of SOPs and to ensure training on relevant SOPs.Preparation, review and approval of risk assessment investigation report if required.Responsible for any other assignment given by Head- Quality.Qualification: B.Pharma / M.ScExperience: 8-10 Years
Job Title
Panacea Biotec | Job Title Assistant Manager – Vendor Management