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Quality Control (Assistant Manager)for Pharma Comapny in Vizag

10.00 to 12.00 Years   Vishakhapatnam   24 Jul, 2021
Job LocationVishakhapatnam
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaGeneral / Other Software
EmploymentTypeFull-time

Job Description

Roles and ResponsibilitiesJob Title: Quality Control (Assistant Manager /Deputy Manager)Company: Leading Pharma API Bulk Drugs Company in Vizag LocationDesignation: Assistant Manager/Deputy ManagerReporting to: Senior ManagerNo. of Positions: 2Division: API Bulk DrugsDepartment: Quality Control Job Location:Vizag Location Qualification: MSc (Full Time)Years of Experience:10 to 12 Years Salary Range: 10 LPAContact person: Mr.Zabi Moghal Mobile: 8105301588 Email: zabi@bvrpc.comRoles:

  1. Initiation of change controls, deviations, OOS, Incidents and Invalidations and other related documents like Job/Work orders etc.,
  2. Departmental investigations and preparation of investigation reports.
  3. Preparing and review of Raw materials, intermediates, Recovery, API and packing materials Spec s, STP s along with raw data, ATR, and certificate of analysis.
  4. Internal audits/external audit preparation for QC.
  5. Maintaining data integrity in QC.
  6. Preparation and review of all departmental procedures like SOPs, Calibration procedures, analytical documents, Preventive maintenance procedures, Protocols, Reports, stability summary sheets and trend data sheets.
  7. Preparing and Review of Cleaning validation protocols, stability and hold time study protocols and its reports.
  8. Working standard Management.
  9. Procuring of Reference standards and Qualification of In-house standards.
  10. Maintenance of laboratory equipment and laboratory cleaning.
  11. Maintenance of chemicals in Quality Control.
  12. Handling and maintenance of stability chambers.
  13. Chemical and glassware indent.
  14. Samples sending to ETP for destruction.
  15. Daily monitoring and recording of Temperature and Humidity records, lab cleaning records.
  16. Control samples / retain samples management.
  17. Stability samples packing, inception, withdrawal and stability sample management.
  18. Review of Instrumental and Wet analysis data (HPLC, GC, UV, IR, and Potentiometer) of Raw materials, Intermediates, In-process, packing materials, Residual solvents, Finished product and Stability samples.
  19. To perform and review of calibrations of Instruments located in Quality control department.
  20. CAPA implementation.
  21. Coordinating with all departments for smooth operations of department.
  22. Good Laboratory practices and Compliance.
  23. To attend the cGMP and GLP trainings as per schedule and training of analysts.
  24. To perform the activities by following the safety norms, SOP s and adhering with company policy.
Industry: Pharmaceutical & Life Sciences Functional Area: Production , Manufacturing , Maintenance Role Category: Production/Manufacturing/MaintenanceRole: Quality Assurance/Quality Control ManagerEmployment Type: Full Time, Permanent ,

Keyskills :
salesmisaccountstatbankingcontinuous improvement facilitationbulk drugstime studylife sciencesraw materialsdata integrityquality controlcleaning validationlaboratory equipmentpreventive maintenanceetpapi

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