Summary
Overview
Work History
Education
Skills
Certification
Languages
Languages
Websites
Timeline
Generic
Rohit Rathor

Rohit Rathor

Hyderabad

Summary

Results-driven chemical engineer with over 10 years of experience in pharmaceutical manufacturing. Proven expertise in optimizing production processes and enhancing product quality. Currently employed at MSN Laboratories, contributing to significant operational improvements.

Overview

11
11
years of professional experience
1
1
Certification

Work History

<ul><li>Production Block Incharge Job Role: Operations, Control and Monitoring</li><li>1. All activities related to production and monitoring the process as per SOPs.</li><li>2. Communicate day to day process deviations and breakdowns of the equipment to concerned persons.</li><li>3. Check and implement the process for cleaning of equipment as per the schedules.</li><li>4. Responsible for housekeeping and implementation of day to day cleaning of process area & clean room.</li><li>5. Preparation, review and approval of monthly Reports and BPRs BCRs, OOS, Deviation, investigations reports, validation protocols reports, validation reports.</li><li>6. Responsible for preparation of daily production planning and ensuring the same.</li><li>7. Production planning, ensuring that the batches are produced as per planning and meeting the dispatch targets.</li><li>8. Ensure proper utilization of equipment and manpower as and when required.</li><li>9. Planning and monitoring during execution of the process validation.</li><li>10. Manpower planning. Monitor the project modification activities.</li><li>11. Responsible to handle production processes.</li><li>12. Implementation of new technology w.r.t. process equipments or facility.</li><li>13. Supporting quality assurance team for DMF submission.</li><li>14. Executing and supervising training, validation, qualification and calibrations protocols.</li><li>15. To perform visual inspection and certification of cleaned equipment after product change over cleaning as per standard operating procedure.</li><li>CGMP:</li><li>1. Following departmental standard operating procedures (SOP) and providing suggestions for SOP simplification and any other improvements.</li><li>2. Making sure all the documents and checklist are verified before and after manufacturing.</li><li>3. Ensuring retention and destruction of records are maintained in a department.</li><li>4. Verifying status labeling of accessories, in-process instruments, containers, area & equipment.</li><li>5. Performing contemporaneous (on time) document entries.</li><li>EHS:</li><li>1. Following Environment, Health and Safety policies and practices.</li><li>2. Making sure personnel health, hygiene and organization practices are followed.</li><li>3. To conduct risk analysis of product, system, equipment, process as per standard procedure.</li><li>Training</li><li>1. Attaining training as per training need and providing training to sub-ordinates through available software of Learning Management System (LMS).</li></ul>

MSN Group
03.2023 - Current
  • Production Block Incharge Job Role: Operations, Control and Monitoring
  • 1. All activities related to production and monitoring the process as per SOPs.
  • 2. Communicate day to day process deviations and breakdowns of the equipment to concerned persons.
  • 3. Check and implement the process for cleaning of equipment as per the schedules.
  • 4. Responsible for housekeeping and implementation of day to day cleaning of process area & clean room.
  • 5. Preparation, review and approval of monthly Reports and BPRs BCRs, OOS, Deviation, investigations reports, validation protocols reports, validation reports.
  • 6. Responsible for preparation of daily production planning and ensuring the same.
  • 7. Production planning, ensuring that the batches are produced as per planning and meeting the dispatch targets.
  • 8. Ensure proper utilization of equipment and manpower as and when required.
  • 9. Planning and monitoring during execution of the process validation.
  • 10. Manpower planning. Monitor the project modification activities.
  • 11. Responsible to handle production processes.
  • 12. Implementation of new technology w.r.t. process equipments or facility.
  • 13. Supporting quality assurance team for DMF submission.
  • 14. Executing and supervising training, validation, qualification and calibrations protocols.
  • 15. To perform visual inspection and certification of cleaned equipment after product change over cleaning as per standard operating procedure.
  • CGMP:
  • 1. Following departmental standard operating procedures (SOP) and providing suggestions for SOP simplification and any other improvements.
  • 2. Making sure all the documents and checklist are verified before and after manufacturing.
  • 3. Ensuring retention and destruction of records are maintained in a department.
  • 4. Verifying status labelling of accessories, in-process instruments, containers, area & equipment.
  • 5. Performing contemporaneous (on time) document entries.
  • EHS:
  • 1. Following Environment, Health and Safety policies and practices.
  • 2. Making sure personnel health, hygiene and organisation practices are followed.
  • 3. To conduct risk analysis of product, system, equipment, process as per standard procedure.
  • Training
  • 1. Attaining training as per training need and providing training to sub-ordinates through available software of Learning Management System (LMS).

<ul><li>Working in Clean Room (100000 area) Module area. Hands on experience in Handling Powder Process area.</li></ul>

Macleods Pharmaceuticals
02.2022 - 03.2023
  • Working in Clean Room (100000 area) Module area. Hands on experience in Handling Powder Process area.

<ul><li>API/CRAMP manufacturing. Working in production department as Senior Executive.</li><li>Adherence to Standard Operating Procedures, product specifications and Good manufacturing practices.</li><li>Monitoring the process efficiencies. Overall coordination with other departments related to production activities.</li><li>To perform equipment cleaning, In-process product sampling, inspection and storage.</li><li>Achieving the production targets. Production, raw material planning with senior members of production and procurement of the raw materials from the Stores through the Material Requisition Slip.</li><li>Department training coordinator.</li></ul>

Sailife Sciences Ltd
02.2020 - 02.2022
  • API/CRAMP manufacturing. Working in production department as Senior Executive.
  • Adherence to Standard Operating Procedures, product specifications and Good manufacturing practices.
  • Monitoring the process efficiencies. Overall coordination with other departments related to production activities.
  • To perform equipment cleaning, In-process product sampling, inspection and storage.
  • Achieving the production targets. Production, raw material planning with senior members of production and procurement of the raw materials from the Stores through the Material Requisition Slip.
  • Department training coordinator.

<ul><li>1. Working in Production along with R&D team and Doing trail and validation of new products in Pilot Plant.</li><li>2. Trouble shooting during Development and execution.</li><li>3. Performing trial and Validation Batches and generating data preparing trial report, Validation Reports.</li><li>4. Coordinating with production department to take product and getting output.</li></ul>

MSN Group
05.2016 - 02.2020
  • 1. Working in Production along with R&D team and Doing trail and validation of new products in Pilot Plant.
  • 2. Trouble shooting during Development and execution.
  • 3. Performing trial and Validation Batches and generating data preparing trial report, Validation Reports.
  • 4. Coordinating with production department to take product and getting output.

<ul><li>Responsible for taking batch as per BPR.</li><li>Responsible for Monitoring Temperature and pressure.</li><li>Responsible for trouble shooting.</li><li>Responsible for observing Process of Production.</li></ul>

Shilpa Medicare Ltd 100 percent Export Oriented Unit
08.2015 - 05.2016
  • Responsible for taking batch as per BPR.
  • Responsible for Monitoring Temperature and pressure.
  • Responsible for trouble shooting.
  • Responsible for observing Process of Production.

<ul><li>Working in production department as a supervisor and taking product.</li></ul>

Delta fino chem
08.2014 - 08.2015
  • Working in production department as a supervisor and taking product.

Education

B.Tech/B.E. - Chemical Engineering

Ratnagiri Mahrashtra
Ratnagiri Mahrashtra
01.2014

Nashik Mahrashtra - Chemical Engineering

K K Wagh Polytechnic
Nashik Mahrashtra
01.2011

Majalgaon Mahrashtra - Marathi

Shree Sidhesvar Mahvidyalay
Majalgaon Mahrashtra
01.2006

Skills

  • Collaboration and teamwork
  • Microsoft Office proficiency
  • Excel expertise
  • Accountability and leadership
  • Good manufacturing practices
  • Problem solving
  • Documentation management
  • Collaboration and teamwork
  • Microsoft Office proficiency
  • Excel expertise
  • Accountability and leadership
  • Good manufacturing practices
  • Problem solving
  • Documentation management

Certification

Diploma in chemical engineering

Languages

English, Hindi, Marathi, Telugu

Languages

Marathi
First Language
English
Advanced (C1)
C1
Hindi
Advanced (C1)
C1
telagu
Advanced (C1)
C1

Timeline

<ul><li>Production Block Incharge Job Role: Operations, Control and Monitoring</li><li>1. All activities related to production and monitoring the process as per SOPs.</li><li>2. Communicate day to day process deviations and breakdowns of the equipment to concerned persons.</li><li>3. Check and implement the process for cleaning of equipment as per the schedules.</li><li>4. Responsible for housekeeping and implementation of day to day cleaning of process area & clean room.</li><li>5. Preparation, review and approval of monthly Reports and BPRs BCRs, OOS, Deviation, investigations reports, validation protocols reports, validation reports.</li><li>6. Responsible for preparation of daily production planning and ensuring the same.</li><li>7. Production planning, ensuring that the batches are produced as per planning and meeting the dispatch targets.</li><li>8. Ensure proper utilization of equipment and manpower as and when required.</li><li>9. Planning and monitoring during execution of the process validation.</li><li>10. Manpower planning. Monitor the project modification activities.</li><li>11. Responsible to handle production processes.</li><li>12. Implementation of new technology w.r.t. process equipments or facility.</li><li>13. Supporting quality assurance team for DMF submission.</li><li>14. Executing and supervising training, validation, qualification and calibrations protocols.</li><li>15. To perform visual inspection and certification of cleaned equipment after product change over cleaning as per standard operating procedure.</li><li>CGMP:</li><li>1. Following departmental standard operating procedures (SOP) and providing suggestions for SOP simplification and any other improvements.</li><li>2. Making sure all the documents and checklist are verified before and after manufacturing.</li><li>3. Ensuring retention and destruction of records are maintained in a department.</li><li>4. Verifying status labeling of accessories, in-process instruments, containers, area & equipment.</li><li>5. Performing contemporaneous (on time) document entries.</li><li>EHS:</li><li>1. Following Environment, Health and Safety policies and practices.</li><li>2. Making sure personnel health, hygiene and organization practices are followed.</li><li>3. To conduct risk analysis of product, system, equipment, process as per standard procedure.</li><li>Training</li><li>1. Attaining training as per training need and providing training to sub-ordinates through available software of Learning Management System (LMS).</li></ul>

MSN Group
03.2023 - Current

<ul><li>Working in Clean Room (100000 area) Module area. Hands on experience in Handling Powder Process area.</li></ul>

Macleods Pharmaceuticals
02.2022 - 03.2023

<ul><li>API/CRAMP manufacturing. Working in production department as Senior Executive.</li><li>Adherence to Standard Operating Procedures, product specifications and Good manufacturing practices.</li><li>Monitoring the process efficiencies. Overall coordination with other departments related to production activities.</li><li>To perform equipment cleaning, In-process product sampling, inspection and storage.</li><li>Achieving the production targets. Production, raw material planning with senior members of production and procurement of the raw materials from the Stores through the Material Requisition Slip.</li><li>Department training coordinator.</li></ul>

Sailife Sciences Ltd
02.2020 - 02.2022

<ul><li>1. Working in Production along with R&D team and Doing trail and validation of new products in Pilot Plant.</li><li>2. Trouble shooting during Development and execution.</li><li>3. Performing trial and Validation Batches and generating data preparing trial report, Validation Reports.</li><li>4. Coordinating with production department to take product and getting output.</li></ul>

MSN Group
05.2016 - 02.2020

<ul><li>Responsible for taking batch as per BPR.</li><li>Responsible for Monitoring Temperature and pressure.</li><li>Responsible for trouble shooting.</li><li>Responsible for observing Process of Production.</li></ul>

Shilpa Medicare Ltd 100 percent Export Oriented Unit
08.2015 - 05.2016

<ul><li>Working in production department as a supervisor and taking product.</li></ul>

Delta fino chem
08.2014 - 08.2015

B.Tech/B.E. - Chemical Engineering

Ratnagiri Mahrashtra

Nashik Mahrashtra - Chemical Engineering

K K Wagh Polytechnic

Majalgaon Mahrashtra - Marathi

Shree Sidhesvar Mahvidyalay

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