Manufacturing, Production Planning & Execution, GMP, Documentation & Record Keeping, Equipment Handling Safety, Reporting & Coordination.
Synthetic experience from Gram to kilogram scale Experience in handling moisture and light sensitive reagents API’s Analysis and characterization of molecule using techniques Structural interpretation of intermediates and finished products
Operation and Calibration of Analytical Balance Method Development Method Validation Scale up Batch Analysis, Investigating Analysis HPLC Analysis Instruments handling
Handling female worker in assembly(Clean Room), Leadership Skill, Manage 50+ worker in one shift. Packaging Blister/ Sealing Operations Skills, Man Motion Study, Assembly Experience.
Equipment Maintenance & Uptime Compliance & Documentation Utility Systems Management Spare Parts & Inventory Control Safety & Environment Continuous Improvement Team Coordination & Training Project Involvement
Strategic Planning and Implementation Experience of ERP Implementation IT Infrastructure Management Security and Risk Management Project Management Team Leadership and Development Vendor Management Budget Management Compliance
Risk Assessment and Hazard Control Environmental Management Health & Safety Programs Training and Awareness Emergency Preparedness and Response EHS Reporting and Documentation Continuous Improvement Hazop Study
Experience of reviewer data review of method validation. Document review like STP, Protocols and Reports of AMV , verification. Monitoring of daily activities Preparation and review of Validation Protocol, Report, SOP and Specifications, analysis.
Towork asper cGMP Norms. To carry out the processes of different products To make entry in BMR. To follow written SOP To follow instructions given by the Production Executive To ensure batch processing. To report any deviation occurred ONLY FRESHERS
Procurement exp of RM (Import must) Followup with parties for timely delivery Import Docs i.e..DA Payment/LC/Advance/Import license app, Duel Noc App through CDSCO Prep of Purchase Order Vendor Dev & Docs Followup with Clearing agent & Logistics Team
Work as per cGMP norms. To carry out the processes of different product as per the respective approved BMR for QA department. Make entry in BMR while process is in progress. To ensure operational control. To report regarding work to production Head.
Procurement(Import Documentation must) Followup with parties for timely delivery Import Docs i.e..DA Payment/LC/Advance/Import license app, Duel Noc App thr CDSCO Prep of Purchase Order Vendor Dev & Docs Followup with Clearing agent & Logistics Team
Handling female worker in assembly(Clean Room), Leadership Skill, Manage 50+ worker in one shift. Packaging Blister/ Sealing Operations Skills, Man Motion Study, Assembly Experience.
Discuss company’s products features with various stockiest, purchase officers, retailers, pharmacies etc. Implement company’s strategies and through various modes of communication. Maintain Customer Relationship.
Job Description •Calendar,Travel&Email,Management •Travel as & when required with Director for Marketing meeting Required •Excellent communication skills. (Gujarati Read,Write &Speak ) •Strong organizational,and time management
fixed asset register, proper calculation of depreciation, MOA, P&L on sale provide F.A details for Govt scheme, loans from banks Inter company reconciliation statutory & internal audit balance sheet Tax audit General ledger scrutiny & rectification
Production Planning & Execution, GMP & Regulatory Compliance, Documentation & Record Keeping, Process Control & Improvement, Team Supervision & Training, Equipment Handling & Maintenance, Quality & Safety, Reporting & Coordination.
Autocad Must To work as per cGMP norms. Unkeep engineering QMS,SOPs, Formats, Layouts, Calibration, Validation records. Follow up with vendors, materials, proposals. To take measurements & prepare drawings in AutoCad. Send CV's - hr1.src@surajlok.com
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