Sruthi S

Experience

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  Biozone Research Technologies Pvt. Ltd

  Apr 2016 - May 2016

  Summer Intern

  It was a 15 day internship at Biozone Research Technologies Ltd ,Chennai. I got an exposure to various herbal compounds and hands on training in extraction of various plant metabolites , Secondary metabolite detection – Qualitative ,Quantitative estimation of Phenols, Flavonoids andTannins, Free radical scavenging activity-DPPH , Antimicrobial activity-Well/Disc, Minimum inhibitory Concentration ,Separation of secondary metabolite – TLC

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  BioLim Centre for Science & Technology

  Jun 2017 - Jul 2017

  Internship Trainee

  Project Title -Food Technology (Biofortification) Root Beer Production using two different roots with different strains and to determine the changes in carbonations, flavors and odors.Tools or techniques used: 1. Estimation of Glucose by Dinitro Salicylic Acid by (DNS) Assay method. 2. Estimation of protein by Biuret method. 3. Determination of titratable acidity in Root Beer. 4. Detection and Estimation of Ethanol. 5. Determination of Colony forming units (CFU) in bacteria. Outcome: Gained exposure to different biochemical assays. Show less

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  Camillotek India Pvt Ltd

  Apr 2022 - Mar 2023

  Quality Control Executive

  . Produced Formulation specification documents, along with a support factory.• Assist in Research collaboration for structural-functional claims , clinical trials and in preparation of Scientific study /Clinical Reference for Finished Formulation.. Working on analytical aspects of different delivery forms of nutraceutical ingredients like Lutein, Beta Cryptoxanthin, Alpha & Beta Carotene, Lycopene, Capsaicin, Curcumin etc.• Preparation of Certificate of Analysis (COA) , Material Safety Data Sheet (MSDS) for raw materials and finished goods.• Maintaining of Batch Records and Blending Records• Preparations of SOP ( Standard Operating Procedure) & Reference in Sample Preparation• Monitor industry news, competitive analysis and implement communication/ differentiation strategies to explore new business. Impart product training / technical support for business• Developing & executing technical marketing communication strategies, sales support tools like Power Point Presentation, Brochures, talk sheets, fast facts, online web description, white papers• Event Management of workshops, seminars, convention organized by the company and Web page update for e‐commerce site related to technical details of products and customer support.• Prepared samples for Consumer testing and benchmarking studies. Provided them to the market for consumer analysis• Record all experiments in the Record book with clearly defining the experiment details and actions planned.• Assist in conducting timely and in-depth investigations to resolve non-complaint product or packaging. Review ingredients to ensure they are compliant with company standards and industry regulations• Monitor food / Nutraceutical development process to ensure products are made consistently every time. Coordinate outside testing by third parties. Collect samples for internal and external review Show less

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  Aura Biotechnologies Private Limited (AURA BIOTECH)

  Apr 2023 - now

  Quality Assurance & Quality Control

  Conducting routine analysis of raw materials, in-process and finished formulations under supervision and according to Standard Operating Procedures (SOPs). Temperature Monitoring of clean rooms, Environmental Monitoring and Water Analysis. Held responsible for sampling of Raw material, Packing material & analyzing the various parameters mentioned in the Certificate of Analysis (COA) and writing the Analytical Test Report for the same. Experience in issuing line clearance at every step of batch manufacturing. Review and approval of QMS activities such as change control, deviation, OOS, OOT, investigations, market complaints, validation protocols, and CAPA as needed. Review of batch manufacturing records, generating deviation reports and CAPA reports. Participated in handling internal audits (ISO13485:2016) and good knowledge on (ISO 9001: 2015). Supported the team in obtaining ISO 13485: 2016 certification and further assisted the company to step into the regulatory registration as a medical device manufacturer for obtaining the manufacturing License (State & CDSCO) and Import License as per MDR (CDSCO). To maintain and monitor the performance of the Quality management systems (ISO 9001, ISO 13485) of the company and ensure meeting the requirements of the appropriate bodies of the national standard and regulations. Participated in external & surveillance audits by regulatory and notified bodies. Interpret test results, compare them to established specifications and control limits, and make recommendations on the appropriateness of data for release. Review and approval of internal, external calibration, validation of instruments and preventive maintenance schedules, ensuring activities are carried out as per the defined schedule. Compiling data for documentation of test procedures and prepares reports. Reviews data obtained for compliance to specifications and reports abnormalities. Train other analysts to perform laboratory procedures Show less