Assistant PD Manager

Interested candidates who meet the requirements are encouraged to apply online.

Only shortlisted candidates will be contacted for the next stage of the selection process.

No TA/DA will be provided for attending the interview.

The interview will be held at 95, Central Basabo, Sabujbagh, Dhaka-1214.

Assist in regulatory inspections and compliance audits.

Prepare requisitions for raw and packaging materials required for new product development.

Develop recipes and annexures for submission to the Drug Administration.

Conduct lab, pilot, stability, trial, and scale-up batches for new products.

Review and optimize existing product formulations based on complaints, stability issues, or cost-saving requirements.

Prepare and maintain product specifications, formulations, process sheets, validation protocols, analytical methods, manuals, dossiers, SOPs, and cGMP/ISO-related documents.

Conduct stability and hold-time studies according to approved protocols and ensure proper analytical method validation.

Monitor pharmaceutical manufacturing activities to ensure compliance with GMP standards.

Perform additional responsibilities assigned by the PD, QA, QC, and Production Managers.