Job Description

  • Start-To-Finish
  • Solutions For Air
  • Solutions For Water
  • Solutions For Process
  • Case Studies
  • Projects
  • Blog

Function: Quality Assurance & Documentation

Reports to: Assistant General Manager

Location: Andheri (HO)

Responsibilities

  • FACILITIES, UTILITIES, PROCESSES, CLEANING AND EQUIPMENTS, DOCUMENTATION AND IMPLEMENTATION
  • MASTER IN FDS, FAT AND SITE QUALIFICATION, COMMISSIONING AND VALIDATION DOCUMENTATION.
  • FACILITY COMMISSIONING AND INSTALLATION OF INJECTABLE LINE I.E. LIQUID & LYOPHILIZED
  • RESPONSIBLE FOR EXECUTION OF INSTALLATION, OPERATIONAL & PERFORMANCE QUALIFICATION OF EQUIPMENTS. RESPONSIBLE FOR REVIEW AND EXECUTION OF SIP VALIDATION, AUTOCLAVE VALIDATION, FREEZE DRYER (LYOPHILIZER), DEPYROGENATION TUNNEL AND VIAL FILLING, STOPPERING AND SEALING MACHINE WITH CRABS.
  • 21 CFR COMPLIANCE AND COMPLAINT ENVIOURMENT
  • AUTOMATION INTEGRATION FROM PLC, SCADA, BMS.
  • AWARE ABOUT BMR - BATCH MANUFACTURING RECORD AND IMPLEMENTATION OF SAME WITH OSD, GRANULATION , INJECTABLE LINE EQUIPMENT’S.
  • UNDERSTANDING OF URS AND THE PROCESS FLOW DIAGRAM AND IMPLEMENTING IT IN THE QAP OF THE EQUIPMENT / SYSTEM TO BE MANUFACTURED.
  • ABILITY TO COMMENT ON THE FABRICATION DRAWING FOR THE REQUIREMENTS OF PROCESS AND SAFETY.
  • IFAT REPORT AND DEVIATION REPORTING, MAKING SNAG LIST AND INVESTIGATION OF PROCESS DEVIATION / COMPLIANCES MISSED DURING MANUFACTURING TO THE ROOT CAUSE ANALYSIS.
  • CONTROLLING OF DOCUMENTATION APPROVAL FROM CLIENT / CONSULTANT IN LINE WITH PROCESS VALIDATION AND CLEANING VALIDATION.
  • MAKING THE QUALIFICATION PROTOCOLS i.e., DQ, FAT, SAT, IQ, OQ, PQ FOR STANDARDIZATION TEMPLATE FOR ALL EQUIPMENT / SYSTEM. THESE TEMPLATES AS CONTROLLED COPY AND RELEASE VERSION TO APPOINTED VENDOR TO COMPLY.
  • LEADING CHANGE CONTROL, DEVIATION & CAPA IN THE DEPARTMENT.
  • SAMPLING OF VALIDATION BATCHES & COMPILATION OF REPORT.
  • VENDOR QUALIFICATION INPUTS FOR SELECTION OF VENDOR BASED ON ITS TECHNICAL CAPABILITIES AND MANUFACTURING CAPACITIES.
  • PREPARATION & REVIEW OF SOP FOR QC PROCESS AND ITS WBS.
  • CLEAN ROOMS, HVAC, BLACK UTILITIES AND CLEAN UTILITIES VALIDATION PROTOCOL AND INTERNAL FAT PROTOCOL / REPORT MAKING.
  • MANAGE ISO QUALIFICATIONS ISSUES AND MAINTAIN ALL OFFICIAL DOCUMENTATION.
  • EXPERIENCE IN AUTOCAD. AND ERP FOR QC STAGE – APPROVAL / DISAPPROVAL

Certification / Training In Areas Of

USFDA, MHRA, ANVISA, TGA, WHO, MOHAP-UAE, ISO-QMS/EMS & OHSMS


Job Details

Role Level: Not Applicable Work Type: Full-Time
Country: India City: Mumbai ,Maharashtra
Company Website: http://www.fabtechnologies.com Job Function: Technical Writing & Documentation
Company Industry/
Sector:
Other

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