BAMMIDI PAPARAO

• Total Experience: 15 Years
  Current Organization: Ocimum Labs Pvt. Ltd.
  Experience at Ocimum Labs: 2.6 Years
  Department: Production / Manufacturing.
• Roles & Responsibilities
  Monitoring and executing manufacturing activities as per approved Batch Manufacturing Records (BMRs).
  Handling reactor charging, process monitoring, sampling, and batch completion activities.
  Coordinating with QA, QC, Warehouse, Engineering, and EHS departments for smooth production operations.
  Ensuring compliance with GMP, safety, and SOP requirements.
  Monitoring critical process parameters and maintaining batch records.
  Supervising shift operations and manpower management.
  Investigating process deviations and implementing corrective actions.
  Supporting process improvements, yield enhancement, and productivity initiatives.
  Coordinating equipment cleaning, line clearance, and preventive maintenance activities.
  Ensuring timely completion of production schedules and dispatch commitments.

For 4.7 years of experience as an Executive, you can highlight the following roles and responsibilities:

• Executed process development and optimization experiments for APIs and intermediates.
• Supported scale-up activities from laboratory to pilot and commercial manufacturing.
• Monitored plant batches and provided technical support during production campaigns.
• Investigated process deviations, OOS/OOT results, and implemented corrective actions.
• Prepared and reviewed batch manufacturing records (BMRs), SOPs, protocols, and reports.
• Coordinated with QA, QC, Production, Warehouse, and Engineering departments.
• Performed data analysis and interpreted HPLC, GC, and other analytical results.
• Conducted impurity profiling, root cause investigations, and process troubleshooting.
• Evaluated raw material vendors and supported technology transfer activities.
• Maintained compliance with GMP, safety, and regulatory requirements.
• Mentored junior staff and ensured timely completion of assigned projects.
• Contributed to yield improvement, cost reduction, and process robustness initiatives.

Sr. Executive - Production Department
STYRAX PHARMA PVT. LTD., Parawada, Andhra Pradesh
November 2015 – September 2020

• Roles & Responsibilities
• Executed and monitored pharmaceutical manufacturing operations in compliance with cGMP and SOP requirements.
• Supervised batch manufacturing activities and ensured adherence to Batch Manufacturing Records (BMRs).
  Operated and monitored production equipment such as reactors, centrifuges, dryers, and related processing systems.
• Ensured timely completion of production schedules while maintaining product quality and safety standards.
• Coordinated with QA, QC, Warehouse, Engineering, and EHS departments for smooth plant operations.
• Monitored critical process parameters and reported deviations, incidents, and abnormalities to management.
  Performed line clearance, equipment cleaning verification, and area preparation before batch execution.
• Maintained production documentation including logbooks, BMRs, equipment records, and shift reports.
  Trained and supervised production operators and contract manpower on GMP and safety practices.
• Participated in process improvements, yield enhancement initiatives, and cost-reduction activities.
• Ensured compliance with safety procedures, environmental regulations, and workplace housekeeping standards.
• Supported validation activities, process qualification batches, and regulatory audits.
  Key Achievements:
• Successfully managed commercial production batches with zero critical deviations.
• Contributed to process optimization initiatives resulting in improved productivity and operational efficiency.
• Maintained high standards of GMP compliance during internal and external audits.

• jr. Executive - Production (3.3 Years Experience) | Key Roles & Responsibilities
• Executed and monitored batch manufacturing activities as per BMR/SOP requirements.
• Ensured adherence to cGMP, safety, and quality standards during production operations.
• Coordinated manpower allocation and shift-wise production activities.
• Monitored critical process parameters and ensured smooth plant operations.
• Maintained production records, logbooks, and batch documentation.
• Coordinated with QA, QC, Warehouse, Engineering, and EHS departments for uninterrupted production.
• Investigated process deviations and implemented corrective and preventive actions (CAPA).
• Tracked production yields, cycle times, and process efficiencies to achieve production targets.
• Trained and supervised operators and technicians on SOPs and safety procedures.
• Supported process optimization, scale-up activities, and continuous improvement initiatives.
• Ensured proper utilization of raw materials, solvents, and equipment to minimize losses.
• Participated in audits, regulatory inspections, and compliance-related activities.