B.Pharma Job Vacancies in Palghar

Working in Tally Prime Accounting till finalization Vendor payments

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.

Operate RO, DM and Softner as per Instruction from Boiler Operator.Take in process samples as per instruction and send to lab.Note down plant parameter readings in Log Book as per SOP.Maintain good House Keeping in plant with the help of labour.

Sell a variety of chemicals to be used in different industriesKeep management informed by submitting activity and results reports, such as daily call reports, weekly work plans, and monthly and annual territory analysis.Monitor competition by gathering current marketplace information on pricing, products, new products, delivery schedules, merchandizing techniques.Service existing accounts, obtains orders, and establishes new accounts by planning and organizing daily work schedule to call on existing or potential sales outlets and other trade factors.

Injectable Experience is mandatoryKnowledge of QAMS SystemPreparation & review of MPCRs and BMRPreparation & review the SOP, Risk assessment and Protocol (e.g. URS/DQ) of various equipment, facility and utilities.Prepare , review the audit report as per regulatory requirements.Handling of Change Control, Deviation and Incident.Root cause analysis and effectiveness of Corrective & Preventive action for Compliance and implementation after recommendations.Preparation of Investigation and impact assessment.Preparation and review of investigation report generated by deviation.Coordination with other departments for closing the corrective & preventive (CAPA) of events against the audit Compliance.To ensure cGMP & GDP compliance in routine activities as per the current regulatory guidance.

Devise procedures to inspect and report quality issues Monitor all operations that affect quality Supervise and guide inspectors, technicians and other staff Assure the reliability and consistency of production by checking processes and final output Appraise customers requirements and make sure they are satisfied Report all malfunctions to production executives to ensure immediate action Facilitate proactive solutions by collecting and analyzing quality data Review current standards and policies Keep records of quality reports, statistical reviews, relevant documentation and perform statistical analysis Communicate with external quality assurance officers during on-site inspections Devise and review specifications for products or processes Ensure adherence to health and safety guidelines as well as legal obligations Oversee all product development procedures to identify deviations from quality standards Inspect final output and compare properties to requirements Approve the right products or reject defectives Keep accurate documentation and Solicit feedback from customers to assess whether their requirements are met Submit detailed reports to appropriate executives Be on the lookout for opportunities for improvement and develop new efficient procedures WHO GMP requirement, complied all the non conconformities. Carried out all for ISO & WHO GMP, Handle Safety audit.KEY REPONSIBILITES Review & Preparations of Quality Management system documents. Review, preparation & Implementation of SOPsQUALIFICATION & VALIDATION Preparations & execution of qualification and validation of various manufacturing & packing equipments.PROCESS VALIDATION Preparations & Execution of process validation activity.

We are looking for 50 Insurance Advisor Posts in Mumbai with deep knowledge in Direct Marketing,Life Insurance,Insurance Sales,Financial Consultancy and Required Educational Qualification is : Higher Secondary, Secondary School, Vocational Course, Diploma, Advanced/Higher Diploma, Professional Degree, Other Bachelor Degree, B.A, B.Arch, B.C.A, B.B.A, B.Com, B.Ed, BDS, BHM, B.Pharma, B.Sc, B.Tech/B.E, LLB, MBBS, BVSC, MD/Medicinae Doctor, Post Graduate Diploma, M.A, M.Arch, M.C.A, M.B.A/PGDM, M.Com, M.Ed, MS/Master of Surgery, M.Pharma, M.Sc, M.Tech, LLM, MVSC, CA, CS, DNB, ICWA, Integrated PG, Other Doctorate Degree, Some Tertiary Coursework, Ph.D/Doctorate, MPHIL, DM/Doctorate of Medicine

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

R/M & P/M Dispensing, Reconciliation, Calculation mfg. of Injectable plantWashing Area Monitoring, ONLINE BMR, Logbook, formats, SOP, must have working in Autoclave, Vial, Ampoule, DHS M/c, DecodingManpower HandlingDocumentation & Formats, SOPRequired Candidate profileB. Sc. /B. Pharm/M.Sc/M.Pharm with injectable mfg - Responsible for Injectable Sterile, Aseptic mfg of pharma - formulation injectable plant, must have knowledge of Audit Documentation, Responsible for SOP.

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)

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.