Mohasin
Muzaffarnagr
Summary
Quality-driven professional specializing in sterile products, recognized for effectively organizing workflows and coordinating resources to achieve challenging objectives. Demonstrates strong problem-solving skills and a persistent approach to operational challenges. Proven decision-making and team-building capabilities, complemented by a clear and open communication style.
Overview
11
11
years of professional experience
Work History
Assistant manager
Somerset Therapeutics Pvt. Ltd.
Bangalore
04.2025 - Current
- Coordinated daily production schedules based on resource availability and priorities.
- Ensured compliance with cGMP, achieving zero accidents in production area.
- Preparation and review of the URS.
- Execution of FAT for new equipment.
- Preparation of SOPs and BMRs.
- Review IQ, OQ, and PQ of new equipment.
- Conducted media-fill batch processing to verify product sterility and quality.
- Trained production technicians on equipment operation and safety protocols.
- Prepared and reviewed documentation for batch manufacturing records and operational logs.
- Participated in qualification and validation of autoclave, HVAC, manufacturing vessels, and other equipment.
- Maintained comprehensive knowledge of aqueous and non-aqueous batch manufacturing processes.
- Supported project teams with planning and execution of change control procedures.
Assistant manager
Brawn laboratories ltd
Faridabad
10.2021 - 03.2025
- Coordinated daily production schedules based on resource availability and priorities.
- Monitored adherence to cGMP standards to maintain quality control in all processes.
- Trained production staff on equipment operation and safety procedures to enhance team capability.
- Conducted regular inspections of manufacturing equipment to ensure proper functionality.
- Prepared and reviewed documentation for batch manufacturing records and operational logs.
- Implemented process improvements that enhanced efficiency and reduced waste in production.
- Facilitated cross-departmental collaboration to streamline production workflow and resolve issues.
- Evaluated production metrics to drive continuous improvement initiatives and operational excellence.
- Participated in the qualification and validation of production equipment to meet regulatory standards.
Production Executive
Sentiss pharma
Nalagarh
07.2020 - 09.2021
- Monitored production line performance to identify and rectify inefficiencies.
- Operated production machinery to ensure efficient manufacturing processes.
- Assisted in inventory management, tracking raw materials and finished goods.
- Participated in training sessions to enhance knowledge of production techniques and safety measures.
- Documented production activities accurately to maintain compliance with regulatory requirements.
- Identified opportunities for process improvements to enhance overall production efficiency.
- Maintained cleanliness and organization of the production area to support operational efficiency.
- Utilized problem-solving skills to address production challenges swiftly and effectively.
- Participated in cross-functional meetings to discuss production updates and challenges.
- Cleaned up work area at end of shift to maintain safe working environment.
- Communicated with team members regarding tasks assigned during shift.
- Followed safety protocols while operating machines and equipment.
- Assisted in setting up production lines for manufacturing processes.
- Monitored production line operations to ensure efficiency and accuracy.
- Tracked production data such as number of items produced per hour, day, week.
- Adhered strictly to established guidelines and procedures while performing duties.
- Utilized computer software programs to record details related to production process.
- Calibrated machines to adhere to quality standards and maintain required productivity levels.
Production Sr.Executive
Brawn laboratories ltd
Faridabad
04.2016 - 03.2020
- Performing and documenting a line clearance check before starting the new batch to ensure no materials, ampoules, or vials from the previous batch remain.
- Accurately recording all necessary details in batch manufacturing records or a logbook.
- Ensuring all operating personnel are correctly gowned to prevent contamination.
- Verifying the continuous and correct supply of all necessary utilities (WFI, DM water, and air).
- Ensuring the area is cleaned and free from previous products
- Sterilization of ampoules and vials in DHS.
- Filter integrity was taken before and after filtration.
- CIP/SIP of the manufacturing tank before batch manufacturing, and completion of the activity after manufacturing.
Production Chemist
Eurolife healthcare Pvt. Ltd.
Roorkee
08.2014 - 04.2016
- Ensuring all compounding vessels are properly cleaned in place, and sterilized in place before use.
- Performing and documenting a line clearance check to verify the area is free of materials from the previous batch.
- Monitoring and controlling critical processes, like temperature and mixing time.
- Completing the batch manufacturing record in real time, recording all steps of manufacturing, filtration, and in-process checks.
- Filter integrity is taken pre- and post-, and recorded in the batch manufacturing record.
- SHWSS verified after the sterilization of IV infusion bottles.
Skills
- Positive attitude
- Quick learner
- Basic computer skills and applications
- Team leadership
- Cross-functional teamwork
- Friendly, positive attitude
- Self motivation
Key Roles Responsibilities
- Responsible for updating on self-hygiene
- Responsible for preparation, review, revision, control, and implementation of standard operating procedures of the sterile manufacturing department
- Responsible for the preparation and review of the master documents of production
- Responsible for the preparation and review of protocols and reports based on the requirements
- Responsible for document management, like BMRs, BPRs, and Master SOP
- Responsible for the handling of change control, deviations, CAPA, investigations, etc., or preparation of production planning on a monthly and daily basis as per the requirement and availability of materials
- Responsible for preparing the daily production report as per the production achieved
- Responsible to follow cGMP, GDP, and discipline in the department, and to ensure that all personnel follow the same
- Responsible for checking that all equipment and lines are in validated and calibrated status
- Responsible for checking that all the records and log books related to washing, manufacturing, filling, sealing, and sterilization of equipment
- Responsible for giving training to all the subordinates
- Responsible for operations like manufacturing, filling, and sealing operations
- Responsible for ensuring cleaning, sanitization, and operations of machines as per standard operating procedures
- Operation of clean-in-place and sterilized-in-place of manufacturing and filtration vessels
- Responsible for implementing and maintaining the quality system, and ensuring compliance in end-to-end manufacturing and aseptic filling operations
- Ensure all documentation complies with GDP and ALCOA principles
- Prepare and maintain a quality risk assessment for equipment and processes
- Initiate change control forms, coordinate with cross-functional teams for impact assessment, and manage pre-approval and closure
- Prepare and review protocols and reports of new equipment qualifications
- Handling and review of URS
- To be involved in the project activities
- To be involved in the FAT execution of new equipment
- Prepare and review protocols and reports of DQ, IQ, OQ, and PQ
- Execution of IQ, OQ, and PQ of new equipment
- Coordinate with the cross-functional team for GxP compliance qualifications of new equipment
- Co-ordinate with the vendor regarding the qualification of new equipment
- Preparation of SOPs related to new equipment
- Having sound knowledge and experience about the manufactured product
- Having knowledge of the aqueous and non-aqueous batch manufacturing
- Review of the batch manufacturing record, batch filling record
- Successfully handle aseptic simulation process
- Preparation of interventions protocol of new machine
- Responsible for training and operator qualification in the aseptic area
Equipment Handled
- Autoclave (machine fabric, Getinge, Truking)
- Manufacturing and filtration vessels (Adam Febriwerk, Praj, and ZETA)
- Amp./vial washing machine, depyrogenation tunnel (Truking)
- Terminal sterilizer (machine fabric and trucking)
- PH meter (Thermo Scientific, Lab India, and Mettler Toledo)
- Integrity tester (Sartorius, Palltronic, and Millipore)
- SIP and CIP module (Adam Febriwerk and ZETA)
- Do meter (Labtonics and Mettler Toledo)
- Glove port integrity tester (Truking and Qualitus)
- Ophthalmic machine (Bosch, Romaco)
- Vial filling and sealing machine (Laxmi, Truking)
- Ampoule filling machine (United, Truking)
- Lyophilizer (LSI)
- PFS (Truking)
Qualification
Bachelor of Pharmacy, Shri Ram college of pharmacy, Karnal, Haryana, 2009-2014
Mobile Numbers
- +918279803653
- +918650010405
Languages
- Hindi
- English
Hobbies and Interests
- Reading books
- Playing Cricket
Personal Information
- Father's name: Sh. Safik Ahamad
- Date of birth: 15/07/92
- Gender: Male
- Marital status: married
Disclaimer
I hereby declare that all the information mentioned above is true to the best of my knowledge
Place: Bengaluru
Timeline
Assistant manager
Somerset Therapeutics Pvt. Ltd.
04.2025 - Current
Assistant manager
Brawn laboratories ltd
10.2021 - 03.2025
Production Executive
Sentiss pharma
07.2020 - 09.2021
Production Sr.Executive
Brawn laboratories ltd
04.2016 - 03.2020
Production Chemist
Eurolife healthcare Pvt. Ltd.
08.2014 - 04.2016