Supv Production - Compression (Goa)

Who we are Together we re on a mission to make good health more affordable and accessible to help millions around the world enjoy healthier lives It s a mission that bonds our people across nearly 60 countries and a rich diverse variety of nationalities and backgrounds Working here means working with the world s leading manufacturer of generic medicines and the proud producer of many of the products on the World Health Organization s Essential Medicines List Today at least 200 million people around the world take one of our medicines every single day An amazing number but we re always looking for new ways to continue making a difference and current people to make a difference with How you ll spend your day Responsible for upkeep of Compression area in Production Responsible for supervising the Compression area in Production Preparation and review of SOP s and other documentation in manufacturing areas Handling of SAP R 3 system Manufacturing related transactions To prepare and review the investigations related to Deviations OOS OOT Market complaints Exception reports etc To initiate review and impact assessment of Quality management systems as part of investigation such as Change controls CAPAs Risk assessment etc Signing of equipment qualification related documents as a business owner To review and ensure compliance calibration preventive maintenance of all machines in manufacturing areas Responsible to perform Glorya EDMS related activities Performing batch manufacturing activities as per BMR instruction Documentation of all activities in areas worked Daily production planning and execution Coordination with cross functional departments for smooth functioning of production activities Review of executed batch manufacturing records Material storage areas management Ensure Standard Operating Procedure compliance To comply with the cGMP practices Undergoing the training as per the identified training needs Training and utilization of the manpower allotted Training and development of the manpower allotted in the area to meet the business need To execute all the tasks assigned by immediate Supervisor HOD Designee To follow the normal safety precautions in production department Responsible for maintaining disciplined work culture in manufacturing area To ensure readiness of the department for regulatory inspections and ensure their compliance Management of inspection readiness Program in the Production Department Participate in the regulatory inspections and internal and external audits Identification of Shop floor related Improvement Project and implement best Practices in the Production Department To ensure compliance to data integrity as per laid down system and procedure Your experience and qualifications B Pharm M Pharm 6 years of experience Teva s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva s global policy that equal employment opportunity be provided without regard to age race creed color religion sex disability pregnancy medical condition sexual orientation gender identity or expression ancestry veteran status national or ethnic origin or any other legally recognized status entitled to protection under applicable laws We are committed to a diverse and inclusive workplace for all If you are contacted for a job opportunity please advise us of any accommodations needed to support you throughout the recruitment and selection process All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience Apply on Kit Job: kitjob.in/job/4mcycn