Libra Group of Companies

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Summary

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

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.

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.

Transport facilities (subject to availability of Car)

Work at office

Full Time

Dhaka (Mirpur)

To apply for this job email your details to admin@chakricircular.com