Pharmacist

Job Title:Pharma Production & Documentation Executive (Schedule M Compliance) Qualification:B. Pharma/B.Sc. / M.Sc. in Pharmaceutical Sciences, Chemistry, Microbiology, Biochemistry, or related field Experience:3 years (Freshers with good knowledge of GMP can also apply) Location:BORANADA , JODHPUR Job Summary:We are looking for energetic and responsible candidates to support our pharmaceutical manufacturing unit in accordance with Schedule M norms. The role involves preparing essential documents, conducting analysis, maintaining manufacturing and quality records, and ensuring compliance with current Good Manufacturing Practices (cGMP). Key Responsibilities:📄 Documentation:Prepare and maintain Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR). Draft and update Standard Operating Procedures (SOPs), protocols, logs, and production documentation. Record equipment cleaning, area sanitization, and material usage as per Schedule M norms. Ensure real-time, error-free, and audit-ready documentation in compliance with GMP. 🧪 Analysis & Monitoring:Assist in in-process checks during manufacturing and packaging. Monitor critical parameters and deviations during batch processing. Coordinate with the QA/QC team for sample testing and batch release. 🗂️ Record Maintenance:Maintain logs for equipment calibration, cleaning, and maintenance. Track and file records for materials, labels, utilities, and environmental conditions. Ensure retention of records and samples as per regulatory timelines. ✅ Compliance & GMP:Adhere to Schedule M and GMP guidelines strictly. Participate in internal audits and implement CAPAs where needed. Support in regulatory inspections and documentation readiness. Desired Skills:Knowledge of Schedule M and Good Manufacturing Practices (GMP) Good understanding of pharmaceutical manufacturing processes Accurate and disciplined approach to documentation Proficiency in MS Office (Word, Excel) and data entry Ability to work in a team under compliance-driven environments