Key ResponsibilitiesProduction DocumentationPrepare, review, and issue Batch Manufacturing Records (BMR) and Batch Production Records (BPR)Maintain daily production logs, shift reports, and production summariesEnsure timely and accurate documentation of production activitiesSOP & Record ManagementDraft, revise, and control Standard Operating Procedures (SOPs) related to productionMaintain document control registers, master lists, and archival recordsEnsure only approved and current versions of documents are in circulationCompliance & Audit SupportEnsure documentation complies with ISO / GMP / Safety / Statutory requirementsSupport internal, customer, and regulatory auditsAssist in closure of audit observations related to documentationCoordination & SupportCoordinate with Production, QA, EHS, and Maintenance teamsCollect production data for monthly MIS and performance reportsSupport deviation, change control, and CAPA documentationData Accuracy & ControlVerify completeness, accuracy, and legibility of all production recordsEnsure timely submission of documents to QA or relevant departmentsQualifications & Experience🎓 Education:B.Sc. Chemistry / Diploma / BE (Chemical) or relevant qualification💼 Experience:2–5 years of experience in production documentation in Chemical / Pharmaceutical / Specialty Chemical industry
