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Job description

**Roles & responsibilities:** - To receive instructions from AM / Manager / GM. To plan the work as per instructions from department head. - To track the daily exhibit / site shift product's trail, engineering, Exhibit & Validation (not limited to) batches manufacturing and monitor it's progress constantly. - To organize, supervise and control the activities of Technology Transfer department. - To co-ordinate and co-operate with various departments like Raw material store, Engineering, Quality Assurance, Administration, Information Technology, Operational Project, Quality Control, Production etc. for smooth functioning of Technology Transfer department. - To check and update various documents and records, ensure production records filled online during batch manufacturing. - To check and maintain housekeeping of the department. To enforce latest developments in GMP, SOP's etc. - To observe and report to the seniors of Product / Material / Machine for their abnormal identified behaviour during production process. - To counter check Raw Materials Dispensing and to recheck the material prior to their use in production processes. - To ensure that the Quality, Health, Safety, Environment policy and procedures are followed. - To prepare documents of New Product (ANDA) and site shift products (which includes CCF, MFC, BMR, QFR, ISP, PPQP, QRM, ESR TT Protocol, TT Report & PPQR (not limited to). - To prepare documents for MES activity. - To check, **(i)** Sampling request to Quality Assurance Department **(ii)** Material requirements requisitions **(iii)** Received batch from RM department - To check / verify, **(i)** Daily Work in progress status. - To achieve required production targets as per the budgetary norms. - Handling of change parts. To ensure proper follow of company's rules and regulations. - To ensure that all documents are complete in all respect prior to next stage of processing. - To write requisition slips of Auxiliary Materials / Stationary materials etc. of daily use. - To procure and control the utilization of such materials. - To maintain optimum stock level of such materials for smooth functioning of department. - To carry out any additional responsibility entrusted from time to time. - Monitoring of Production process at each stage. - To understand and follow all written procedure and manufacturing instructions mentioned in the respective batch record or any other quality document before starting production activity. - To monitor constantly the CAPA of deviations, OOT and OOS to complete within time frame. - To perform the investigation within timeframe related to quality system i.e. deviation, OOT and OOS. - To be in communication with TRC and it's cross functional team for coordination and knowledge sharing of new site transfer products. - To ensure that all SOP trainings are fulfilled on periodic basis. - To coordinate activities like visit, document transfer and monitoring (but not limited to) related to manufacturing of products at CMO site. **Preferred candidate profile:** Candidates should have in-depth experience in FTT department. This is a plant based job. OSD pharmaceutical experience is Mandatory. **Qualification:** B. Pharm. / M. Pharm. **Location:** Dahej, Gujarat **Total Experience:** 3 to 8+ Years **Designation**: Executive Interested Candidates please share your updated CV on **akshitsharma@torrentpharma.com** .