Summary
Work History
Education
Skills
Languages
Accomplishments
Personal Information
Timeline
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CHETAN ROHIDAS PATIL

CHETAN ROHIDAS PATIL

Jalgaon,Maharashtra

Summary

I am a Quality Assurance Professional equipped with a B.Sc. in Chemistry and substantial hands-on experience in the pharmaceutical industry. My expertise lies in In-Process Quality Assurance, focusing on GMP compliance, line clearance protocols, and real-time production monitoring. I take pride in my attention to detail and commitment to ensuring product quality and safety in every task I undertake

Work History

jr.officer

Intas Pharmaceuticals Ltd
Ahmedabad, Gujarat
- 03.2024
  • Real-time production monitoring
  • Line clearance inspections
  • Batch documentation & compliance
  • Deviation identification & resolution
  • Line Clearance: Rigorously checking that no materials, labels, or containers from the previous batch remain in the area before the next batch starts.

Education

B.Sc. - Chemistry

North Maharashtra University

ITI -

ITI Dhule

HSC -

Nashik Board

SSC -

Nashik Board

Skills

  • Quality Assurance Competency
  • Detail-oriented professional specializing in GMP compliance and batch documentation

Languages

English, Advanced

Accomplishments

  • Achievement in Quality Assurance, Specialist in ensuring strict adherence to GMP standards and quality protocols in the pharmaceutical industry
  • Compliance & Audit Readiness
  • Zero-Defect Audits: Successfully led or supported a facility through a major regulatory audit (e.g., USFDA, MHRA, WHO-GMP) with zero 'Critical' or 'Major' observations.
  • Audit Readiness: Achieved a 100% internal audit compliance score by implementing a proactive 'Daily Walkthrough' checklist that identified and corrected 20+ potential GMP violations before they were flagged.
  • Documentation Excellence: Reduced batch record errors by 30% through the implementation of a real-time review system, ensuring data integrity (ALCOA+ principles).
  • Risk Management & Problem Solving
  • CAPA Implementation: Successfully closed 50+ CAPAs within stipulated timelines, resulting in a 25% decrease in recurring deviations over a 12-month period.
  • Root Cause Analysis (RCA): Led a cross-functional investigation into a recurring contamination issue, identifying a faulty gasket and preventing an estimated $200k in potential product loss.
  • Deviation Reduction: Reduced minor deviations by 20% by introducing a 'Quality at Source' initiative that empowered shop-floor operators to self-correct minor alignment issues.
  • Training & Leadership
  • Team Proficiency: Trained over 50+ production staff on Revised Schedule M or updated SOPs, leading to a measurable 15% increase in team compliance during spot checks.
  • SOP Optimization: Authored or revised 15+ Standard Operating Procedures (SOPs) to streamline in-process checks, making them more user-friendly for operators while maintaining strict compliance.

Personal Information

  • Date of Birth: 11/13/97
  • Nationality: Extra Field

Timeline

jr.officer

Intas Pharmaceuticals Ltd
- 03.2024

B.Sc. - Chemistry

North Maharashtra University

ITI -

ITI Dhule

HSC -

Nashik Board

SSC -

Nashik Board

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