The ChromoSep Technologies established in Ahmedabad, Gujarat, India. We manufactured and deals in below products :1. HPLC Columns a. Reverse Phase Columnsb. Normal Phase Columnsc. Ion Exchange Columnsd. Size Exclusion (Gel Filtration) Columnse. Chiral Columnsf. Affinity Columnsg. Hydrophilic Interaction Liquid Chromatography (HILIC) Columns, h. Monolithic Columns, i. Hydrophobic Interaction Chromatography (HIC) Columns, j. UHPLC… Show more The ChromoSep Technologies established in Ahmedabad, Gujarat, India. We manufactured and deals in below products :1. HPLC Columns a. Reverse Phase Columnsb. Normal Phase Columnsc. Ion Exchange Columnsd. Size Exclusion (Gel Filtration) Columnse. Chiral Columnsf. Affinity Columnsg. Hydrophilic Interaction Liquid Chromatography (HILIC) Columns, h. Monolithic Columns, i. Hydrophobic Interaction Chromatography (HIC) Columns, j. UHPLC Columns2. SPE Cartridge’s3. Quechers4. Sorbent / media Show less

Cliniapps Pvt. Ltd. based out at ahmedabad, Gujarat was established with following services related to CRO and Pharma SERVICES:1) Medical Writing2) Regulatory Functions (India/EU/USA/Australia/SA)3) Scientific Writing4) Translation and Back Translation of ICF5) Monitoring of Clinical Study (Clinical and Bioanalytical )5) Ethics Committee 6) 03rd Party Archiving7) Cultural Activity

Worked as Senior Manager with ECTS Pvt. Ltd., Ahmedabad. My role here Involved:1. Creates and executes project work plans and revises as appropriate to meet changing needs and requirements.2. Identifies resources needed and assigns individual responsibilities.3. Monitoring and tracking the project delays and other issues/risks impacting project performance and delivery timelines.4. Coordinating/following study timelines of projects between departments and updating the… Show more Worked as Senior Manager with ECTS Pvt. Ltd., Ahmedabad. My role here Involved:1. Creates and executes project work plans and revises as appropriate to meet changing needs and requirements.2. Identifies resources needed and assigns individual responsibilities.3. Monitoring and tracking the project delays and other issues/risks impacting project performance and delivery timelines.4. Coordinating/following study timelines of projects between departments and updating the project status to the HODs and to the Business Head. 5. Review of Protocol, ICD, CRF’s and CSR.6. Review of the Standard Operating Procedures (SOPs) of the Organization. Show less

Worked as Project Lead/Associate QC in CPCD department with Jubilant Clinsys Ltd., Noida. My role here Involved:1. Creates and executes project work plans and revises as appropriate to meet changing needs and requirements.2. Identifies resources needed and assigns individual responsibilities.3. Monitoring and tracking the project delays and other issues/risks impacting project performance and delivery timelines.4. Coordinating/following study timelines of projects between… Show more Worked as Project Lead/Associate QC in CPCD department with Jubilant Clinsys Ltd., Noida. My role here Involved:1. Creates and executes project work plans and revises as appropriate to meet changing needs and requirements.2. Identifies resources needed and assigns individual responsibilities.3. Monitoring and tracking the project delays and other issues/risks impacting project performance and delivery timelines.4. Coordinating/following study timelines of projects between departments and updating the project status to the HODs and to the Business Head.5. Maintaining study milestones and timelines throughout the project6. Manage day-to-day operational aspects of a project and scope.7. People Management, working with multi-cultural clients.8. Coordinate with sponsors concerning size, standards, conditions and timing of research9. Establish, implement and manage processes and procedures covering configuration management, including change control, risk & issues management and documentation management.10. Sending triggers to the concerned department for the timeliness and Quality.11. Ensuring the compliance with various audits like USFDA, ANVISA, and DCGI etc. 12. Review of Protocol, ICD, CRF’s and CSR.13. Review of the Standard Operating Procedures (SOPs) of the Organization.14. Conducting system audit and facility audit along with the Principal Investigator. Show less