Pharma Production incharge ( Indore);

Job Description

Mail:- info@naukripay.com

pharmaceutical production incharge supervises daily shop-floor manufacturing operations. They ensure medicine batches are produced safely, on schedule, and in strict compliance with current Good Manufacturing Practices (cGMP) and regulatory guidelines.Key ResponsibilitiesBatch Execution: Monitor granulation, mixing, compression, coating, or sterile filling processes as outlined in the Batch Manufacturing Record (BMR).Compliance & Documentation: Ensure real-time, accurate entries in BMRs, equipment logbooks, and line-clearance checklists.Team Management: Assign daily shift targets, manage shift rosters, and train operators on safety and standard operating procedures (SOPs).Equipment Oversight: Coordinate with engineering and maintenance teams for routine cleaning (CIP/SIP), calibration, and breakdown repairs.Quality & Safety Coordination: Report deviations, manage line clearances, and assist Quality Assurance (QA) and Quality Control (QC) during investigations and audits.Required QualificationsEducation: Bachelor’s degree in Pharmacy (B.Pharm), Pharmaceutical Chemistry, or Chemical Engineering.Experience: 3 to 6 years of hands-on plant manufacturing experience in a regulated pharma environment.Core Skills: Deep knowledge of cGMP standards, strong leadership, active problem-solving, and clear shift-reporting abilities.If you are tailoring this for a specific application, tell me:What dosage form is the plant making (tablets, liquids, injectables)?Is this for a shift incharge or a department head role?

Requirements
Pithampur, Sector 1, Madhya Pradesh | Pharma & Production Supervisor | Manufacturing Operations | CTC: Rs. 3.75 LPA We are looking for a hands-on Production Supervisor to manage day-to-day operations on the chemical/pharma manufacturing floor, ensuring safety, quality, and output targets are consistently met. Qualification B.Sc / M.Sc (Chemistry / Biochemistry) or B.Pharma Experience Minimum 2 years in Chemical or Pharma manufacturing Location Pithampur, Sector 1, Madhya Pradesh CTC Rs. 3.75 LPA ROLES & RESPONSIBILITIES Supervise and coordinate daily production activities on the shop floor to meet output schedules. Monitor batch manufacturing processes in compliance with SOPs, GMP, and safety regulations. Lead and guide a team of operators and technicians; assign tasks and track performance. Ensure proper documentation of batch records, logbooks, and production reports. Coordinate with QC, maintenance, and stores for smooth material flow and equipment uptime. Identify process deviations and implement corrective actions promptly. Enforce safety protocols and conduct toolbox talks and shift briefings. Assist in yield improvement, waste reduction, and cost optimization initiatives. REQUIRED SKILLS & TOOLS Strong understanding of chemical/pharma manufacturing processes and equipment. Knowledge of GMP, cGMP, and EHS (Environment, Health & Safety) standards. Familiarity with batch processing equipment: reactors, centrifuges, dryers, distillation units. Ability to read and interpret process flow diagrams (PFDs) and P&IDs. Proficient in production documentation and MIS reporting. Working knowledge of ERP or manufacturing execution systems (MES) is an advantage. PREFERRED QUALIFICATIONS B.Sc / M.Sc in Chemistry, Industrial Chemistry, or Biochemistry. Prior experience in API or specialty chemical manufacturing. Exposure to ISO 9001 / ISO 14001 / OHSAS 18001 certified environments. Demonstrated ability to lead teams of 10+ operators on rotating shifts. Local candidates from Indore / Pithampur region preferred. Microbiologist | Quality Control & Assurance | CTC: Rs. 5.0 LPA We are seeking an experienced Microbiologist to strengthen our QC lab capabilities in pharma/API manufacturing, ensuring microbial testing, environmental monitoring, and regulatory compliance. Qualification B.Sc / M.Sc in Microbiology or Applied Microbiology Experience Minimum 3 years in Pharma / API manufacturing Location Pithampur, Sector 1, Madhya Pradesh CTC Rs. 5.0 LPA ROLES & RESPONSIBILITIES Conduct microbial testing including Total Viable Count (TVC), bioburden, and sterility tests. Perform environmental monitoring of clean rooms, production areas, and utilities (water, air). Prepare, review, and approve microbiology-related SOPs, protocols, and test reports. Investigate OOS (Out of Specification) results and prepare deviation/CAPA reports. Maintain and calibrate microbiological lab equipment and culture media. Ensure all testing activities comply with IP, BP, USP, and WHO guidelines. Support regulatory inspections (CDSCO, WHO-GMP, customer audits) with data and documentation. Train lab staff on aseptic techniques and microbiology best practices. REQUIRED SKILLS & TOOLS Proficiency in microbial identification techniques: culture methods, gram staining, PCR-based ID. Hands-on experience with laminar airflow (LAF), biosafety cabinets, autoclaves, and incubators. Knowledge of pharmacopoeial standards: IP, BP, USP microbiology chapters. Expertise in water microbiology testing (WFI, purified water, process water). Familiarity with LIMS (Laboratory Information Management System). Strong documentation skills and understanding of data integrity principles (ALCOA+). PREFERRED QUALIFICATIONS M.Sc in Microbiology, Pharmaceutical Microbiology, or Biotechnology. Experience in WHO-GMP or Schedule M compliant pharma ROLES & RESPONSIBILITIES Perform chemical and physical analysis of raw materials, in-process samples, and finished products. Operate and maintain analytical instruments: HPLC, GC, UV-Vis spectrophotometer, Karl Fischer titrator, etc. Prepare and standardize analytical reagents, reference standards, and working solutions. Document test results in lab notebooks, LIMS, and COA (Certificate of Analysis) generation. Investigate OOS/OOT results and participate in root cause analysis. Execute method validation, method transfer, and stability studies as required. Ensure compliance with pharmacopoeial specifications (IP, BP, USP, in-house methods). Support internal and external audits with accurate records and traceability. REQUIRED SKILLS & TOOLS Hands-on expertise with HPLC (reverse phase, ion exchange) and GC (headspace, direct injection). Proficiency in wet chemical techniques: titration, pH, viscosity, density, particle size analysis. Working knowledge of IP, BP, and USP test methods and acceptance criteria. Experience with LIMS and analytical data management systems. Strong understanding of GLP (Good L