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Newburgh, IN USGC HolderAvailability: Street Address Hours NoticeSummary: Jayantilal is Pharma manufacturing operation s personal with extensive experience and proven track record of a successful production management key person and a key to quality management system and project implementation, handled solid, liquid orals and ointments dosage form.
Accomplished effective design, development, FDA approval for new facility and first production run for Tables, liquid orals and ointment forms. Executed successful design and development of Solutions, Suspension, ointments, tablets/capsules dosage forms Tablets Manufacturing facility. Work as a project team member, completed supervision of installation of machines, departments, services lines, water circulation loop system, steam lines, carried out Design qualification, Installation Qualification, operation qualification and performance qualification equipment s. Documentations for entire new production facility for Tablets, liquid oral and ointment production facility. Passionate, industrious team player, self-motivated to utilize completely accumulated experience and knowledge to the fullest extent possible, becoming a valuable asset for the right company.
Skills: Technical Capacity (Microsoft suite, especially Excel). Communication Proficiency. Performance Management Result Driven Strong decision-making skills. Organizational and leadership skills. Interpersonal skills Problem-solving skills Time Management Autonomy Standard Operation procedures for following department, Personal / human resource department Production departments Ware house raw material, finished goods, Packaging material- primary and secondary packing materials. Maintenance, department, Quality control departments Quality Assurance departments, Calibration of equipment s and tools Good manufacturing practices, Good documentation practices Good laboratories practices, Audit , Validation
Change control SOP Out of specification SOP FDA liaising,
Face External Audit with FDA Authorities Training, Format Worker efficiency validation, Master Formula record, Batch processing and packaging record, Vibratory sift 20 sifter screen diameter
Powder bins, Powder Suction line, Fluid Bed Drier Stem /electrically heating 30/60/120 kg capacity/steam/electrical heated Octagonal blender 250 kg capacity Sigma Blender 150 Kg. Ribbon mixer 1000 kg capacity Double compression rotary tablet machines, Bolus Compression Machine Tablet inspection belts, Coating pans 45/60
Strip sealing machine 4 tracks, 6 tracks, Blister foaming and sealing machine. Auto cartooning machine Conveyer belt packing line Reaction vessel 5000 liter capacity With Load cells Batch manufacturing vessel with load cells Homogenizer in built Sparkler filter press Liquid storage vessels, Liquid measuring and auto filling line Oil phase melting vessel 1000 kg capacity Water phase vessel 1500 kg capacity Ointment manufacturing vessel 2000 kg capacity with inbuilt homogenizer Ointment Storage vessel 2000 kg. Capacity Ointment filling four head semi auto filling machine connected to auto cartooning and tube placing unit and carton closing and batch coding machine and wrapper thermos sealing unit onlineProfessional Experience:United Fulfillment Supplier Inc., (St. Louis, Missouri, USA) Jun2020 0ct 2020Packer in Kitting Department, packer, labeler, sticker fixing,Tjmaxx Distribution Center, (Evansville, 47711, Indiana)) December 2020-May 2021As Associates packer
TaylorMade Golf company as Contract employee from DXE staffing, Evansville, Indiana, 47711 As Associates packer from 9th June 2021 to December 2022.
Essential Functions And Key Responsibilities Pull stock from storage shelves in accordance with shipping documents/orders; verify stock for accuracy. Select appropriate shipping carton, pack product efficiently and to prevent damage. Accurately enter data into computer terminals to prepare shipping labels, and affix labels to cartons. Use voice pick devices to pick product on forward pick lines (golf balls, bags, clubs, etc.) Perform customer value added services (VAS) such as price ticketing, inserts and labeling requirements. Assemble shipping cartons according to outbound order requirements. Operate pacer function to include managing flow of work to VAS and Sort, and review any quality errors captured by WMS. Operate tape machines safely and efficiently to maintain quality while keeping pace with the flow of boxes. Scan and process packages using World Ship system. Conduct all tasks in accordance with satisfactory safety practices. Maintain a neat and orderly work area. May be required to lead/train employees in adequate standards of work, as designated by management. Perform other related duties and assignments as required.Biopharm ltd, (Nairobi, Kenya) Jun2010 Nov2011Production Manager Set and manage new project to commence commercial production, Liaison and face audit and obtain manufacturing license from Kenyan Drug Authorities Prepare All Documents to monitor, operate, manufacturing, in-process quality control test, manufacturing facility cleaning and comply to the Kenyan Drug authorities Commence Production for tablet and ointment manufacturing facilities. Develop production and in-process quality control system to analyzing production, quality testes, quality assurance, preventive maintenance scheduling to reduce machine down time and detection of online non confirmation to quality and correction online to avoid reprocessing and production loss.Health biotech ltd, (Baddi, Himachal Pradesh, India) Jun2009 Jan 2010Production Manager Set and manage production schedule strictly to meet deadline. Co-ordinate raw materials and active pharmaceutical ingredients, primary and secondary packaging materials procurement, preventive maintenance, training to sub-ordinates, optimize process, rigid In-process quality control testing, operation wise strict human power consumption monitoring to achieve production plans
Maxter-Biogenics ( Malku-Manjara, Himachal Pradesh, India) Nov2007 Jun2009Plant Manager Planned and dedicated precise work load to trained team members to achieve production in time.
Corrected formulations problems and revised manufacturing process to achieve 35% increase in production Goal. Update total quality management system, documentation and prepare to face WHO-GMP audits. Renewed all documentations, SOPs, MFR, BPPR, Qualification, Validation, Total quality system documents, quality manuals to revised manufacturing process and updated for conformance to revised standards and policies.Paras Pharmaceutical Ltd. (Baddi, Himachal Pradesh, India) April 2005 Oct 2007Senior Production Manager Documentations for entire new production facility for Tablets, liquid oral and ointment production facility, Prepare WHO GMP audits and proud to say this unit accredited WHO GMP certificate. Stream line initial scale up production problemsCitypharm Pharmaceutical Industry, (Khartoum, Sudan) Aug 2003 Jan 2005Plant in charge/ manager Diagnose root cause for production of tablets, teach good practices to maintain and safe punches to achieve good quality product. Prepare Master Formula records, revised Batch Process and Packing records. Train the co-worker how to maintain machines for longer productivity.
Themis Pharmaceuticals, (Vapi, Gujarat) Oct 2001 Jul 2003Plant manager Managed manufacturing operations of tablet, liquid orals departments as per cGMP, Achieved production schedules through inter-department coordination and development of department employees through orientation and trainingAnkur Drugs and Pharma Ltd, (Daman UT, India) Apr 2000 Oct 2001Production manager Manager contract manufacturing work of Cipla ltd. Performed troubleshooting of production issues, complex investigation of deviations, identified root cause and proposed corrective actions Generated information and compiled reports relating to scheduling, production goals, equipment and maintenance issues as requestedMicron Pharmaceuticals, (Vapi, Gujarat, India) Mar.1995 Apr 2000Production manager Managed manufacturing operations of tablet, General capsules and Beta lactam groups capsules, liquid orals and ointments departments as per cGMP, Achieved production schedules through inter-department coordination and development of department employees through orientation and training. Performed troubleshooting of production issues, complex investigation of deviations, identified root cause and proposed corrective actions Generated information and compiled reports relating to scheduling, production goals, and equipment and maintenance issues as requested.Bonanza drugs and Pharmaceuticals ltd,(Vapi, Gujarat, India) Oct.1989 Feb1995
Production manager Performed troubleshooting of production issues, complex investigation of deviations, identified root cause and proposed corrective actions Generated information and compiled reports relating to scheduling, production goals, equipment and maintenance issues as requestedNep Pharmaceuticals,(Vapi, Gujarat, India) Mar-86 to Nov.89Production in charge Manufacturing of Batches of tablets and hard Gelatin capsule filling. Monitor and record Mfg facility parameterDuphar-Interfran Ltd,(Vapi, Gujarat, India) Aug-80 to Mar-86Supervisor FDA liaison,
Batch tablets manufacturing,
IPQC, Batching packing,
Product change over,
Supervision Contract manufacturing facility
Technical expert person for tablets Dept approved by FDA GujaratCyanamid India Ltd. (Atul , Gujarat, India)Oct-78 to Aug.80Supervisor Batch dispensing
Batch manufacturing in process quality control,
Batch re-conciliation
Production change over Technical expert person for capsule Dept approved by FDA GujaratL M College of Pharmacy,(Ahmedabad, Gujarat, India)July-75 to Oct.-78As Assistant lecturer in Pharmaceutics Department Tutor, and demonstration for practical Supervise examinations, conduct examinations
Evaluation of student performance in examinationEducation: L.M College of Pharmacy, Gujarat University, India, Master of Pharmacy June1973- June 1975Major Subject: Pharmaceutics Higher Class 59.11%
L.M College of Pharmacy, Gujarat University, India, Bachelor of Pharmacy, First Class June1969- June 1973 |