RR
Ravi Rathor
Senior Officer at Oman Pharmaceutical Products Co. LLC
Salalah, OmanWork Experience
Oman Pharmaceutical Products Co. LLC
Sep 2023 - Present -1 yr, 10 months
Oman
- Job Details:Oversee production in the antibiotic block, ensuring smooth execution from dispensing to packing. Execution of production plans in alignment with quarterly manufacturing schedules, ensuring timely delivery and achievement of production targets. Managed manpower by planning shift schedules, assigning tasks, and supervising daily activities to ensure smooth production flow and operational efficiency. Managed SOPs, deviations, and audit compliance activities within the OSD department, ensuring adherence to regulatory and GMP requirements. Preparation and revision of BMRs/BPRs to ensure accuracy, completeness, and compliance with regulatory and GMP standards. Handling of change controls, ensuring effective implementation and timely closure in compliance with quality and regulatory requirements. Participated in audits from various regulatory bodies, including the EU-Hungary, Saudi Arabia, Cameroon, Towa, AET, and MOH, ensuring compliance with global standards and successful audit outcomes.
Troikaa Pharmaceuticals Ltd
May 2022 - Jul 2023 -1 yr, 2 months
India
- Job Details:Preparation and revision of standard operating procedures (SOPs) in accordance with current GMP and regulatory requirements. Handling of change controls, ensuring effective implementation and timely closure in compliance with quality and regulatory requirements. Handling of deviations by conducting root cause analysis, coordinating corrective and preventive actions (CAPA), and ensuring timely documentation and closure in line with QMS protocols. Enhanced operational efficiency by optimizing manufacturing processes and streamlining documentation control, ensuring faster turnaround times and improved compliance. Involved in documentation, SOP development, and process validation during the setup of the facility, ensuring GMP compliance and operational readiness in liquid capsule facility.
Torrent Pharmaceuticals Ltd
Apr 2019 - Oct 2021 -2 yrs, 6 months
India
- Job Details:Handling of granulation operations, including equipment setup, process monitoring, and adherence to batch manufacturing protocols and GMP standards. Managed manpower by planning shift schedules, assigning tasks, and supervising daily activities to ensure smooth production flow and operational efficiency. Execution of monthly production plan by coordinating resources, monitoring progress, and ensuring timely completion of manufacturing targets in compliance with quality standards.
Maxheal Laboratories Pvt. Ltd
Dec 2017 - Mar 2019 -1 yr, 3 months
India
- Job Details:Preparation and revision of batch manufacturing records (BMR) and batch packing records (BPR) in accordance with GMP guidelines to ensure accurate documentation and regulatory compliance. Handling of granulation operations, including equipment setup, process monitoring, and adherence to batch manufacturing protocols and GMP standards. Preparation of master formula records (MFR) to ensure accurate formulation details, batch consistency, and compliance with quality standards. Participated in audits from various regulatory bodies, including the EU-Hungary, Cameroon, Tanzania.
Education
Bachelor's Degree in Pharmacy
R.G.P.V.Jan 2010 - Jan 2014 - 4 yr
Diploma in Computer Application
M.C.R.P.V.Jan 2013 - Jan 2014 - 1 Year
Bachelor's Degree
N.C.H.S. SchoolJan 2009 - Jan 2010 - 1 Year
High School
T.D.S. Academy SchoolJan 2008 - Jan 2009 - 1 Year