Pharma production incharge ( Indore)

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Production Supervisor | Manufacturing Operations | CTC: Rs. 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.QualificationB.Sc / M.Sc (Chemistry / Biochemistry) or B.PharmaExperienceMinimum 2 years in Chemical or Pharma manufacturingLocationPithampur, Sector 1, Madhya PradeshCTC

ROLES & RESPONSIBILITIESSupervise 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 & TOOLSStrong 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 QUALIFICATIONSB.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 LPAWe are seeking an experienced Microbiologist to strengthen our QC lab capabilities in pharma/API manufacturing, ensuring microbial testing, environmental monitoring, and regulatory compliance.QualificationB.Sc / M.Sc in Microbiology or Applied MicrobiologyExperienceMinimum 3 years in Pharma / API manufacturingLocationPithampur, Sector 1, Madhya PradeshCTCRs. 5.0 LPA
ROLES & RESPONSIBILITIESConduct 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 & TOOLSProficiency 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 QUALIFICATIONSM.Sc in Microbiology, Pharmaceutical Microbiology, or Biotechnology.Experience in WHO-GMP or Schedule M compliant pharma/API facility.Exposure to endotoxin/LAL testing, microbial limits testing (MLT), and sterility testing.Working knowledge of 21 CFR Part 211 microbiological requirements is a plus.Prior experience handling regulatory audit responses (CDSCO, NABL, WHO).


Chemical Analyst | Quality Control Laboratory | CTC: Rs. 4.75 LPAWe are hiring a skilled Chemical Analyst to support our QC laboratory operations in pharma and chemical manufacturing — performing analytical testing, maintaining instrument performance, and ensuring product compliance.QualificationB.Sc / M.Sc in Chemistry or Analytical ChemistryExperienceMinimum 3 years in Pharma / Chemical manufacturing QCLocationPithampur, Sector 1, Madhya PradeshCTCRs. 4.75 LPA
ROLES & RESPONSIBILITIESPerform 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 & TOOLSHands-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 Laboratory Practice) and data integrity (ALCOA+).Ability to draft and review analytical SOPs, test procedures, and validation protocols.PREFERRED QUALIFICATIONSM.Sc in Analytical Chemistry, Organic Chemistry, or Pharmaceutical Chemistry.Hands-on experience with LC-MS, ICP-OES, or NIR spectroscopy is a strong advantage.Prior exposure to API or fine chemical QC laboratory environments.Familiarity with ICH guidelines (Q2, Q6A) for analytical method validation.Experience supporting regulatory audits (CDSCO, WHO, customer inspections).To apply, contact HR Sakshi at 9009383833 or email [email protected]