I am currently working with microorganisms. My focus is mainly on the expression and regulation of silent gene clusters which will contribute towards the discovery of novel antibiotics.

Looking for jobs in the field of Pharma/Biotech/Regulatory/Clinical sector

• Good Documentation Practices and Good Manufacturing Practices according to EU guidelines• Quality Control of water, raw materials, finished products• Environmental quality control of production area which mainly involves Active air, Passive air monitoring, Personnel monitoring, Walls and floors monitoring• Routine checks of water for detection of pathogens like pseudomonas sps, staphylococcus sps• Maintenance of aseptic environments along with calibration of the incubators and refrigerators• Participation the media filling to qualify aseptic production• Qualification of personnel and material airlocks

• Good Documentation Practices and Good Manufacturing Practices according to EU guidelines• Quality Control of water, raw materials, finished products• Environmental quality control of production area which mainly involves Active air, Passive air monitoring, Personnel monitoring, Walls and floors monitoring• Routine checks of water for detection of pathogens like pseudomonas sps, staphylococcus sps• Maintenance of aseptic environments along with calibration of the incubators and refrigerators• Participation the media filling to qualify aseptic production• Qualification of personnel and material airlocks

• Good Documentation Practices and Good Manufacturing Practices according to EU guidelines• Quality Control of water, raw materials, finished products• Environmental quality control of production area which mainly involves Active air, Passive air monitoring, Personnel monitoring, Walls and floors monitoring• Routine checks of water for detection of pathogens like pseudomonas sps, staphylococcus sps• Maintenance of aseptic environments along with calibration of the incubators and refrigerators• Participation the media filling to qualify aseptic production• Qualification of personnel and material airlocks

-Dossier formulation- Common Technical Document-Monitoring of existing registrations-Ensuring compliance with regulations set by the Medicines and Healthcare products Regulatory Agency (MHRA)-Maintaining familiarity with company product ranges-Outlining requirements for labelling, storage and packaging-Writing comprehensible, user-friendly, clear product information leaflets and labels