Job Title: Shift In-Charge Production (Pharma)Qualification: B.Sc. ChemistryExperience: 25 years in pharmaceutical production with documentation exposureJob Summary:Responsible for supervising production activities during shifts, ensuring adherence to cGMP, and maintaining proper documentation (BMRs, logbooks, etc.).Key Responsibilities:Oversee shift operations and manpower.Maintain production records as per GMP standards.Ensure compliance with SOPs and safety norms.Coordinate with QA/QC and maintenance teams.Report deviations/incidents promptly.Skills:Strong in pharma documentationGood knowledge of GMPTeam handling and communication skills