Pharma production incharge ( Indore)

Required Skills:

Hindustan Phosphates Pvt. Ltd. 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 / (Chemistry / Biochemistry) or 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 / 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 / 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 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