jayanta banik
dy production manager
About
1. Twelve years of experiences in Pharmaceutical Solid Oral Doses Manufacturing. 2. Approved Competent Technical Person for Solid Oral Manufacturing. 3. Well familiar with SAP PP Module R/6 and R/3 Versions. 4. Extensive exposure in Documentation – SOP, BMR, BPR Preparation. 5. Extensive exposure in Process Validation and Equipment Qualification Activities. 6. Audit exposure – MHRA, ISO, BRC, WHO, US FDA, FDA-Korea. 7. Technology Transfer – execution and implementation. Specialties: 1. Tablet Manufacturing - Wet Granulation,DryGranulation, Compression, Coating, Inspection. 2. Ointment Manufacturing - Emulsion, Suspension type. 3. Production Planning - Planning as per material availability, Maximizing utilization of man and machines, Production plan achievement. 4. SOP Preparation - General, Operation, Cleaning,Calibration. 5. Validation & Qualification - Protocol Preparation,Execution & Report preparation. 6. Projects - New machines
india
valsād
pharmaceuticals
quality management, cgmp, gmp, process validation, regulatory affairs, change control, software documentation, validation, cleaning validation, quality system, v&v, pharmaceutics, manufacturing, pharmaceutical industry, technology transfer, capa, fda, sop, 21 cfr part 11
Experience
dy production manager
macleods pharmaceuticals ltd.
officer - production
wockhardt
* Public Company * 5001-10,000 employees * Pharmaceuticals industry
production chemist
indchemie health specialities pvt. ltd.
* Privately Held * 501-1000 employees * Pharmaceuticals industry
assistant production manager
usv limited
* Overall Departmental responsibilities - Pilot Plant. * Co-ordination with DDRL for new produc. * Handling Deviation, Market complain & CAPA design & implementation
assistant manager
rpg life sciences ltd.
* Production Planning and Scheduling – as per priority and RM/PM availability * Co-ordination with QA, QC, Store and Engineering Department. * Training to subordinate regarding SOP, GMP. * Preparation and review of BMR, BPR, Flow chart. * USFDA Audit Preparations
executive - production
ucb
* Overall responsibilities for tablet manufacturing. * Plan achievement. * Procurement of changeparts. * cGMP training. * Departmental SOP preparation. * Validation & Process development. * Technology Transfer * Installation of new machinaries and Qualification. * Key auditee
Education
umakanta academy
dibrugarh university
jayanta banik's Contact Information
Phone
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