Bridge Pharmaceuticals Ltd.

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Summary

Education

M.Pharm or M.Sc in Chemistry /Bio-Chemistry/Applied Chemistry from any reputed University.

Experience

Additional Requirements

Job Context

Job Location: Factory – West Tengra, Sarulia, Demra, Dhaka.

Job Responsibilities

To perform formulation and process development activities of drug products of all dosage form based on Quality by Design.
To carry out process validation of all type of dosage form.
To be successfully conduct of all types local regulatory and export audit.
Re-formulation of existing products to improve, quality of the products.
Initiating the initial feasibility study followed by pre- formulation study.
Identifying and quantifying raw and packaging material for new products and raising requisition for trial and Pilot batch quantity from Warehouse.
Preparing product recipe and registration documents for submission to Drug Administration Authorities
Manufacturing Lab and Pilot batches after preparation of Manufacturing Record and checking in process quality control parameters.
To prepare the stability schedule &monitor stability samples (lab batch and validation batch); keep in stability chamber for further functions and prepare summary report of stability, stability protocol, summary data sheet.
Preparing new BMR & BPR, Product Data sheet, etc.
Submitting proposals and designs for evaluation by the project team and management before moving to the next stage.
Manage the product creation process from design handoff to production approval.

Full Time

Dhaka (Demra)

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