Anusha Nara

I am a result oriented Bio-tech professional with organisational and leadership capabilities. I have extensive industrial knowledge and 5+ years of experience in equipment handling, validation, product release, sampling and documentation as per GMP requirements to maintain the quality and safety of products. I believe my strongest assets are my self-disciplined professional attitude, accuracy, adaptability and eagerness to learn more to develop the highest standards possible. I am that dynamically work towards the growth of the organization so as I could prove myself. 

• Prepare for production through use of production schedule, studying requirements, clarifying specifications as necessary, calculating calibrations, weighing components, assembling materials and stocking supplies.
• Perform sterilization and maintenance checks including cleaning out-of-place (COP), cleaning in-place (CIP) and servicing in-place (SIP).
• Monitor operation equipment conditions and make adjustments as needed to comply with production requirements.
• Adhere to filling and filtering procedures while calculating dilutions, concentrations and yields.
• Adhere to cGMP or current good manufacturing practices, standard operating methods and legal regulations to maintain a safe and clean work environment.
• Maintaining the hygiene and integrity of the facilities and equipment.
• Document production by accurately completing forms, reports, logs, and records of equipment and batches.
• Following all health and safety procedures and requirements.
• Coordinated with Quality Control and Quality Assurance for deviations, change control, batch production records.
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Bachelors in biotechnology