Roles and Responsibilities Manage production planning, batch processing, manufacturing operations, and plant production to ensure timely delivery of high-quality products. Develop and implement effective strategies for improving productivity, reducing costs, and increasing efficiency in liquid manufacturing processes. Ensure adherence to regulatory requirements by maintaining accurate records of production activities and implementing corrective actions as needed. Collaborate with cross-functional teams to resolve issues related to equipment maintenance, personnel management, and supply chain logistics. Desired Candidate Profile 15-20 years of experience in pharmaceutical industry with expertise in Batch Processing, Manufacturing Operations & Management. Bachelor's degree in Pharmacy (B.Pharma). Strong understanding of GMP regulations and ability to apply them effectively throughout the production cycle. Confident on facing regulatory audits like USFDA, MHRA
Roles and Responsibilities Ensure compliance with GLP guidelines, including investigation of OOS/OOT events and vendor qualification. Maintain accurate records of GLP documents, instruments, and equipment through preventive maintenance schedules. Conduct calibrations on instruments according to CGMP requirements and perform spares management tasks. Implement LIMS system for effective inventory control and HPLC analysis. Perform CAPA activities as needed to resolve quality issues. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Organic Chemistry from a recognized university. Minimum 10-15 years of experience in pharmaceutical industry with expertise in GLP practices. Strong understanding of instrument calibration procedures under cGMP regulations. Proficiency in maintaining IQ, OQ, PQ documentation for laboratory equipment.
Roles and Responsibilities Conduct quality control analysis using HPLC, GC, UV, spectrophotometer, sterile techniques, and other relevant methods. Ensure compliance with USFDA, GMP, GLP regulations during regulatory audits. Develop and maintain SOPs for laboratory operations and testing procedures. Collaborate with cross-functional teams to resolve quality issues and improve processes. Perform stability studies on APIs and finished products as required. Desired Candidate Profile 2-7 years of experience in a pharmaceutical industry setting with expertise in QC analysis. MS/M.Sc(Science) degree in Chemistry or related field; Strong understanding of analytical instruments such as HPLC, GC, UV spectrometer etc., and ability to operate them effectively.
Roles and Responsibilities Conduct market complaint investigations, deviation management, and OOS/OOT handling according to established procedures. Ensure compliance with regulatory requirements through vendor qualification, equipment qualification, cleaning validation, water validation, injectable processing, and process validation. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Develop and maintain documentation related to quality control processes. Provide technical support for product testing and analysis. Desired Candidate Profile 4-8 years of experience in Quality Assurance (QA) or a related field within the pharmaceutical industry. Strong understanding of Good Manufacturing Practices (GMP), Current Good Laboratory Practice (cGMP), and other relevant regulations. Bachelor's degree in Pharmacy (B.Pharma) from an accredited institution.
Roles and Responsibilities Ensure compliance with GLP guidelines, including investigation of OOS/OOT events and vendor qualification. Maintain accurate records of GLP documents, instruments, and equipment through preventive maintenance schedules. Conduct calibrations on instruments according to CGMP requirements and perform spares management tasks. Implement LIMS system for effective inventory control and HPLC analysis. Perform CAPA activities as needed to resolve quality issues. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Organic Chemistry from a recognized university. Minimum 10-15 years of experience in pharmaceutical industry with expertise in GLP practices. Strong understanding of instrument calibration procedures under cGMP regulations. Proficiency in maintaining IQ, OQ, PQ documentation for laboratory equipment.
Roles and Responsibilities Ensure compliance with cGMP guidelines during batch manufacturing of eye drops, injectables, parenteral products, and injections. Monitor production processes to ensure quality standards are met. Conduct regular audits to identify areas for improvement and implement corrective actions. Collaborate with cross-functional teams to resolve issues related to formulation development and process optimization. Develop and maintain documentation for batch records, SOPs, and other relevant documents. Desired Candidate Profile 8-12 years of experience in pharmaceutical industry with expertise in ophthalmic manufacturing. Bachelor's degree in Pharmacy (B.Pharma) or equivalent qualification from a recognized institution. Strong understanding of Batch Manufacturing, Injectables, Parenteral, Eye Drop & Injection processes.
Roles and Responsibilities Monitor and control BMR, BPR, sterility, and other parameters to ensure product quality. Conduct regular inspections of equipment, machinery, and work areas to maintain a clean and organized environment. Collaborate with cross-functional teams to resolve issues related to formulation development, manufacturing processes, and packaging materials. Maintain accurate records of production data, including batch records, inventory management, and material handling. Ensure compliance with GMP guidelines during production activities. Desired Candidate Profile Strong understanding of Good Manufacturing Practices (GMP), Current Good Manufacturing Practice (cGMP), Quality Control (QC), Quality Assurance (QA). Proficiency in working with Ophthalmic products/formulations. Bachelor's degree in Pharmacy (B.Pharma) or equivalent qualification from a recognized institution. 5-10 years of experience in pharmaceutical industry with expertise in formulation development and production.
Roles and Responsibilities Perform breakdown maintenance, corrective maintenance, preventive maintenance, and sterile injectable equipment to ensure optimal performance. Ensure compliance with USFDA regulations during all manufacturing processes. Maintain accurate records of equipment calibration, cleaning validation, and batch production runs. Collaborate with cross-functional teams to resolve issues related to injectables manufacturing. Desired Candidate Profile 4-9 years of experience in pharmaceutical industry with expertise in breakdown maintenance, corrective/preventive maintenance, HPLC analysis, formulation development. B.Tech/B.E. degree in Electrical or equivalent qualification. Strong understanding of USFDA regulations and guidelines for injectable products. Proficiency in performing routine checks on injectable equipment such as syringe pumps, vial washers etc.
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