Title Assistant Manager Vendor Management Panacea Biotec

About Panacea Biotec

Panacea Biotec is a research-based health management company involved in research, manufacturing and marketing of high-quality, affordable pharmaceutical, vaccines and herbal products. The product portfolio includes highly innovative prescription products in important therapeutic areas like pain management, diabetes, cardiovascular, renal disease management, osteoporosis, gastro-intestinal care products and vaccines. 

Panacea Biotec is committed towards disease prevention by introducing Innovative Vaccines that helps to reduce child mortality. Our portfolio consists of worlds first fully liquid Hexavalent vaccine i.e. EasySix (DTwP-Hib-HepB-IPV), the world’s first fully-liquid Pentavalent vaccine i.e. Easyfive-TT (DTwP-Hib-HepB), Oral Polio vaccines (like bOPV, tOPV, mOPV), etc. We have a high-impact pipeline of vaccines including Pneumococcal conjugate vaccines (PCV), tetravalent dengue vaccine, etc. We have supplied 10+ billion immunizations of Polio vaccines in last 20 years, 150+ million immunizations of Novel Innovative fully liquid wP-based vaccines like the wP-Hexavalent vaccine (DTwP-Hib-HepB-IPV). And are a trusted partner for WHO, GAVI and UN Agencies with track-record of sustainable supplies for UNICEF, PAHO, and National Immunization Programs.

Job Description

Job Summary Responsible for Vendor Qualification/disqualification for Pharma division and other activities including GMP assessment and compliance as per regulatory requirements. Responsibilities Vendor 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 vendors To 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.Sc Experience: 8-10 Years,