Coordination of production activity (granulation, encapsulation, coating, support activities) in order to manufacture pharmaceutical products in compliance with GMP principles, EHS system, legal provisions and corporate standards.• proposing solutions for organizing the production activity• performing checks on the coordinated flow according to the manufacturing file of the series• involvement in the activity of investigating deviations from RBPF norms• collaborating directly with the technical staff for the analysis of technical defects, the performance of periodic technical revisions and repairs for the equipment in the production area• identifying the critical parameters and in-process controls required to control the manufacturing process• monitoring the technical problems and proposes solutions to remedy them• proposes solutions to improve the activity on the coordinated flow• controlling the records and the circuit of the Manufacturing Files of the series• ensuring the efficient use of production capacity by properly allocating human and technical resources• pursuing the realization of the production plan• initiating measures and distributes responsibilities to the people he coordinate• defining and delegating clear responsibilities and objectives to subordinates• evaluation, development and motivation of subordinates• signing specific personnel documents (holidays, promotions, warnings)• participation in the investigation of incidents and accidents on the coordinated flow• staff selection and training for the manufacture of Clinical Investigation Drugs

• Verification/ approval of validation and qualification documents;• Verification/ approval of procedures and specifications;• Verification/ approval of risk analysis• Verification/ approval of processing, packaging (serial files) and testing forms (certificates of analysis);• Coordinates changes, participates in the investigation of deviations• Check of supporting documents and completion of statements for customers and authorities: qp for GMP API suppliers, export, TSE / BSE;• Internal/ external audit• Verification and management of quality contracts, take over and sending of requests, updates and management of specific documentation for raw and packaging materials;• Documentation of monitoring reports of suppliers of raw and packaging materials;• Documentation of product risk analyzes and annual reports;• Performance of GMP instruction, ISO 13485, system procedures;• Participation in / and documentation of specific activities for the microbiology laboratory: preparation and verification of culture medium, testing of microbial and endotoxin contamination, sterility control, sampling for microbiological control of utilities and working environment;• Observation and carrying out the entire activity in accordance with the Rules of Good Manufacturing Practice for medicinal products, observes the norms of PM, PSI and Environmental Protection according to the norms in force, the regulations regarding toxic, dangerous substances, precursors for narcotics;• Cooperation with all other departments to ensure the functioning and continuous improvement of the quality system.

I am leading and managing operations for the manufacturing lines, constantly improving and adaptingthe strategies in order to increase efficiency and quality. Starting from protocol sustainability, my aimsas a production supervisor also include the development of the employee skill level through practicallearning – by discovering manufacturing problems on time, I am always able to find solutions in termsof fixing root cause issues. Thus, I can easily train the members of the manufacturing team, so as toavoid such situations in the future.• Coordination of daily fabrication schedule;• Supervision of the fabrication phases: preparation, aseptic processing, aseptic filling, primarypackaging, lyophilization, final sterilization, visual inspection of vials, syringes and Single-Dosecontainers;• Coordination of productivity increase measures;• Implementation of corrective measures for fabrication deviations;• Management of training on production procedures;• Management of raw material consumption;• Development of short- and long-term production scheduling and cost forecasting;• Improvement of productivity by maintaining proper communication with employees;• Management of on-time product delivery;

Dispensation of OTC and prescription medicines.Management of bills, pharmacy inventory and stock orders.Preparation and drafting/ elaboration of magistral recipes.Counselling clients on medication use and discuss possible drug interactions, allergies, or adverseside effects.Reducing customer complaints by discussing their problems and by offering on point solutions;Supervision of dispensing of medicines by pharmacy assistants.Preparation of orders for pharmacy supply.Replacement of the leading pharmacist during his/her absence.Inventory of the pharmacy stock.Implementation of campaigns / promotions.Pharmacy accounting.Staff training.