Sr IPQC officer

Senior QC Officer
Key Responsibilities:Ensure compliance with USDMF (United States Drug Master File) and EU regulatory requirements for all QC-related activities.Review, verify, and close daily QC and production reports, ensuring accuracy and alignment with MIS (Management Information System) requirements.Prepare concise summaries and presentations from daily/weekly QC data for management review.Take lead in weekly and monthly review meetings in the absence of the Manager, ensuring continuity and effective communication across departments.Maintain high standards of data integrity, documentation, and compliance with cGMP guidelines.Coordinate with production, QA, and regulatory teams to ensure smooth operations and timely reporting.Support in audits (internal, customer, and regulatory) by ensuring readiness and compliance of all QC documentation.Key Skills & Competencies:Strong working knowledge of USDMF, EU, and other international compliance requirements.Proficiency in MIS reporting, data analysis, and report preparation.Excellent skills in reviewing technical reports and identifying gaps.Effective communication and presentation abilities for management updates.Leadership qualities to step in during Manager’s absence and ensure seamless team performance.Detail-oriented with strong analytical and problem-solving skills.Qualifications:Diploma in plastic/Degree in Science/Pharmacy/Plastics/related field.4–7 years of experience in Quality Control within the pharma/chemical/polymer industry.Exposure to regulatory audits and compliance requirements (USDMF/EU).