MOHAMMED SAHIL MANSURI
Rajsamand
Summary
Dedicated and detail-oriented quality assurance professional with over 5 years of experience in the pharmaceutical industry. Seeking a challenging QA role to leverage my extensive knowledge of cGMP, QMS, and regulatory compliance to ensure the production of safe and effective pharmaceutical products. Aiming to contribute to the company's commitment to maintaining the highest quality standards, while continuously improving processes to drive excellence and compliance. Proficient in conducting audits, managing documentation, and performing risk assessments to meet regulatory requirements. Skilled in batch record review, CAPA management, and supplier quality management. Adept at leading cross-functional teams to resolve quality issues, enhance processes, and ensure the continuous improvement of quality systems. Strong knowledge of testing, validation protocols, and change control procedures in pharmaceutical environments.
Overview
6
6
years of professional experience
1
1
Certification
Work History
Senior Officer QA
Oman pharmaceutical Products
Salalah
12.2022 - 11.2024
- Ensure compliance with cGMP, FDA, and ICH guidelines in the production of pharmaceutical products
- QMS documentation preparation and management
- Handling (Initiation compliance and closer) and tracking of Change Controls, Deviations and CAPA
- Preparation of SOP’s, APQR, and SMF
- Preparation and review Validation protocols and reports
- Preparation of BMR and BPR’s and SOPs
- IPQA activities (Line Clearance, Sampling and process monitoring etc)
- Review and approve batch records, ensuring all documentation is complete and in compliance with regulatory standards
- Lead internal and external audits, identifying non-conformities and ensuring timely resolution
- Perform risk assessments and implement corrective actions to mitigate identified risks
- Collaborate with cross-functional teams including manufacturing, R&D, and regulatory affairs to ensure adherence to quality standards
- Documentation of Audit compliance
- Handling Departmental Trainings
- Developing standards and specifications for production
- Ensure QA systems and processes for audit readiness
QA-Executive
Macsen Drugs
Udaipur
04.2020 - 11.2022
- Documentation of QMS
- Validation and Qualification documentation review
- Handling and tracking of Change Controls, Deviation, incidents, CAPA etc
- Conduct and Assist External and Internal Audits
- IPQA activities
- Technology Transfer for new products from R&D and Other plants
QA Trainee
Cadila Pharmaceuticals
Ahemedabad
11.2019 - 03.2020
- Performed IPQA activity in granulation, compression and packing
- Review of BMR/LMR and SOP
- Monitoring of manufacturing activities
QA Trainee
Macsen Drugs
Udaipur
08.2018 - 10.2019
- Develop new standards/Specifications for production and design with improvements as per pharmacopoeial standards
- Review of Batch manufacturing, lot manufacturing records, log-records and specifications, sampling instructions, test methods and another Quality Control procedure
- Performing IPQA related activities
- Monitoring of Preventive maintenance program, Calibration program etc
- To ensure that all the records are retained as per the requirement
Education
Masters of Pharmacy -
Bhupal Nobels University
Udaipur12.2021
Bachelors of Pharmacy -
Mohanlal Sukhadiya University
Udaipur12.2018
RSCIT course - computer education
RSCIT
Udaipur, Rajasthan12.2018
Industrial Training -
Cadila pharmaceuticals
Ahmedabad, Gujarat12.2018
Higher secondary education -
Nav Prabhat Sr. Sec School
Rajsamand, Rajasthan12.2014
Secondary education -
B,N.G.S.S
Rajsamand, Rajasthan12.2012
Skills
- Customer complaint handling
- Quality system development
- Quality inspection
- Regulatory compliance
- Quality management systems
- Quality system implementation
- Relationship building
- Performance monitoring
Certification
- Registered Pharmacist
- RSCIT (Computer education)
Hobbies and Interests
- Sports
- Gymming
- Travelling
- Cooking
Languages
Hindi
First Language
English
Advanced (C1)
C1
Arabic
Beginner
A1
Urdu
Upper Intermediate (B2)
B2
Timeline
Senior Officer QA
Oman pharmaceutical Products
12.2022 - 11.2024
QA-Executive
Macsen Drugs
04.2020 - 11.2022
QA Trainee
Cadila Pharmaceuticals
11.2019 - 03.2020
QA Trainee
Macsen Drugs
08.2018 - 10.2019
- Registered Pharmacist
- RSCIT (Computer education)
Masters of Pharmacy -
Bhupal Nobels University
Bachelors of Pharmacy -
Mohanlal Sukhadiya University
RSCIT course - computer education
RSCIT
Industrial Training -
Cadila pharmaceuticals
Higher secondary education -
Nav Prabhat Sr. Sec School
Secondary education -
B,N.G.S.S
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