Bharath Kumar B Email & Phone Number

Bengaluru

Bengaluru, Karnataka, India

Bengaluru, Karnataka, India

Life Science Manufacturing ITQA Compliance

Bengaluru, Karnataka, India

QMS , CSV, DMS & Global Serialisation.

Bengalore

Bengaluru Area, India

Key Job Responsibilities include: Performing quality control analysis of finished pharmaceutical products of various dosage forms as per different pharmacopeia's. Raw materials and API analysis using different techniques like HPLC, GC,UV,IR Preparing method development and validation protocols Review raw data of analysis and report preparation Assign and plan activities for the team members and monitor the progress Communicate with the customer about the progress of the method development activities Prepare and Share the project progress status reports with customers and attend conference with the customer calls as and when required to provide technical clarification Address customer queries on technical aspects and act as interface between the customer and companies commercial team Feasibility check and confirmation for client enquires and proposal preparation and budget planning for the projects Completion of RFP/RFQ and follow up on sales leads End to end Key account management with responsibility of achieving the sales target from key accounts Proposals and Purchase order review and maintenance Sales leads generations and conversion of enquires into order

Ankara, Turkey

Worked onsite for Lab setup and successfully completed GLP audit.

Pune, Maharashtra, India

Research Associate , API Analytical Validations

Pune Area, India

Job Responsibilities include: Analysis of Chemical parameters for. API’s as per USP, EP, JP, IP. Maintenance and calibration of Instrument like, HPLC, Polari meter, UV, IR spectroscopy GC Execute Stability studies within timelines Perform Method validation, Method Transfer and Documentation for validation and transfer  Support to the research teams involved in various projects. Prepare and review Instruments IQ, OQ and PQ. Maintaining Master calibration schedule and Master list of equipment’s. Perform working, In-house standard qualification, and maintenance.  Preparation of Raw data sheets, COA, SOP,  OOS investigation and documentation Comparison of test results against specifications for release or rejection of Materials