Production Chemist Job Vacancies in Palghar

Supervision of Pharma Intermediates manufacturing along with documentation.

A. COORDINATION OF MANUFACTURING SITES FOR TABLETS, CAPSULES, OINTMENT AND INJECTIONS.. IPQC- VERIFICATION OF PARAMETERS ON SITE. B. FOR QUALITY ASSURANCE/QC- REGULATORY AFFARIS - FOR REGISTRATION OF PRODUCTS IN FOREIGN COUNTRY. PREPARATION OF ECTD AS PER FORMAT. VERFICATION OF QUALITY OF PRODUCTS, REPLYING TO QUERY FROM REGULATORY AUTHORITIES FROM FOREIGN AGENCY.

Urgent Requirement For B.Sc/B.Pharm/M.Sc/M.Pharm. For Reputed Pharmaceutical Company

Desired Profile:Candidate Should be B Pharma and FDA ApprovedShould have at least 4 years of experience in tablet CapsuleShould have good communication skillsShould have Audit exposureJob Description:Responsible for activities carried out in Production departmentInvolved in Production of solid dosage forms such as tablets and capsules.To ensure that the Production operations are carried out as per CGMP regulations.Handling and proper utilization of manpower.To approve the instructions relating to production operations and ensure their performanceTo ensure calibrations are done at regular intervalsInvolved in BPR requisition according to production planningMaintaining current good documentation procedures.Rising Raw material requisition according to production planning.4.00-9.00 YearsBachelor of Science (B.Sc), Bachelor Of Pharmacy (B.Pharm)

Equipment handling:Operation and Cleaning of Equipments used in the process area.Trouble shooting of the equipments during process.Production PlanningManufacturing and packing of the products as per BMR / BPR.Material HandlingConsumption of Raw and packing material and solvents in shop floor.Safety, health and environment:On line monitoring of the environment conditions in process area.Desired Certifications: cGMP certificates, Ms Office, SAP preferredFunctional Skills:Handling of unit operations and unit process.Documentation capabilities like filling of BMR / BPR/ECR etc.Knowledge of basic cGMPCritical thinkerProblem solving attitudeAttention to detailsHandling manpower in Shop-floorPlanning of day to day activity

A. COORDINATION OF MANUFACTURING SITES FOR TABLETS, CAPSULES, OINTMENT AND INJECTIONS.. IPQC- VERIFICATION OF PARAMETERS ON SITE. B. FOR QUALITY ASSURANCE/QC- REGULATORY AFFARIS - FOR REGISTRATION OF PRODUCTS IN FOREIGN COUNTRY. PREPARATION OF ECTD AS PER FORMAT. VERFICATION OF QUALITY OF PRODUCTS, REPLYING TO QUERY FROM REGULATORY AUTHORITIES FROM FOREIGN AGENCY.