Quality Control Manager

Libra Group of Companies

Libra Group of Companies

 

Libra Group of Companies

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Summary

  • Vacancy: 01
  • Age: 30 to 45 years
  • Location: Dhaka (Mirpur)
  • Salary: Negotiable
  • Experience: 10 to 15 years
  • Published: 3 Jul 2024

 

Requirements

Education

  • M.Pharm or M.Sc in Chemistry /Bio-Chemistry/Applied Chemistry from any reputed University / Ph.D. (Preferably from Thesis group back ground).

Experience

  • 10 to 15 years
  • The applicants should have experience in the following business area(s):
    Pharmaceutical/Medicine Companies, Medical Equipment, Healthcare/Lifestyle product

Additional Requirements

  • Age 30 to 45 years
  • Experience : 10 to 15 years and at least having a experiences as a Manager for minimum 5 years.
  • Additional Requirements : – Age 30 to 45 years
  • Motivated to work independently and come up with new ideas and directions.
  • Sound in data analysis and analytical, including analyzing and visualizing.
  • Having 5 + years experience in the similar department in a reputed Pharmaceutical Company as a full pledged Manager.
  • Good knowledge in computer operation and analytical skills.
  • Good communication skill both in English and Bengali.
  • Good knowledge in GMP.

Responsibilities & Context

  • Monitoring in process checking all Pharmaceutical and Injection / vial Lypolizer / products etc. and develop New Analytical method.
  • To organize training on cGMP for QA and production personnel’s.
  • Put “Under Test Label”, “Passed Label”, “Rejected Label” of raw materials and packing materials as per requirement.
  • To check water quality parameters of WTP and ETP regularly according to STP(s).
  • Issuance, review and closing of Batch Manufacturing and packing Records and final release of product to market fulfilling international Audit problem.
  • To ensure environmental monitoring in production as per MHRA & FDA guideline.
  • Review and approval of change control form and Project Product Transfer / Technology transfer / Pharmacopeia Change management.
  • Issuance, review and approval of process validation and hold time study protocol and monitoring of validation activities as per MHRA & US FDA.
  • Maintain the good housekeeping of Laboratory & organize the disposal of raw material after release.
  • To conduct in the DGDA Inspection or other internal or external inspection.
  • Handling and operating of all sophisticated QC instruments.
  • Approval of all master documents (e.g. BMR/BPR, SOP, STP, Template etc.) and other formats.
  • To review latest Protocol which is in place for the Pharmaceutical Industries.

Compensation & Other Benefits

  • Mobile bill, Provident fund
  • Lunch Facilities: Partially Subsidize
  • Salary Review: Yearly

Transport facilities (subject to availability of Car)

Workplace

Work at office

Employment Status

Full Time

Job Location

Dhaka (Mirpur)

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