Assistant PD Manager

Job Description

Title: Assistant PD Manager

Company Name: M/s Super Power Pharmaceuticals Ltd.

Vacancy: 02

Age: Na

Job Location: Narsingdi (Belabo)

Salary: Negotiable

Experience:

  • 4 to 5 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies


Published: 2026-02-17

Application Deadline: 2026-03-19

Education:
  • Bachelor of Pharmacy (B. Pharm) / Master of Pharmacy (M. Pharm)

  • Candidate must have computer skill & well conversant with Microsoft Office applications.

  • Candidate should have registration number given by Bangladesh Pharmacy Council.



Requirements:
  • 4 to 5 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies


Skills Required: Product Development

Additional Requirements:

Candidate should have profound knowledge on Standard Operating Procedure (SOP), Pharmaceutical Analysis, Pharmaceutical Calibration/Validation, Process Validation, Proper Documentations, Regulatory Affairs etc. Candidate should be skilled on HPLC, FTIR, UV, ASS, GC, TLC & others QC Equipment’s. Enable to prepare MOA, COA, Method Verifications and Specifications, Method Validations. Coordinate pharmaceutical-related activities for all products.



Responsibilities & Context:
  • Support regulatory inspections and compliance audits.

  • Raising requisition of raw & packaging materials to commercial department for new products as per determined specification.

  • Preparing recipe and annexure for submission to Drugs Administration.

  • Undertaking production of lab batch, pilot batch, stability batch, trial batch, and scale up batch of new products.

  • Reviewing formulation of existing products based on product or market complaints, stability related problems or cost saving need.

  • Preparing and updating all documents i.e. specifications, formulations, process sheet, validation protocol, analytical methods, product manuals, dossiers, procedures and instructions related to cGMP & ISO.

  • Performing stability & hold time stability studies as per protocol and ensure analytical method validation.

  • Monitors drugs manufacturing activities in compliance with the requirements of GMP.

  • Performs other duties as assigned by PD, QA, QC & Production Manager.



Job Other Benifits:
  • Salary Review: Yearly
  • Festival Bonus: 2
    • Salary & other benefits will be considered as per company rules & policies.

    • Special preference will be given to the candidates who have practical knowledge & experience in launching injectable/Sterile Products and attractive salary will be offered to such candidates.



Employment Status: Full Time

Job Work Place:

Company Information:

Gender: Male and Female can apply

Read Before Apply: Please apply only who are fulfilling all the requirements of this job

Category: Pharmaceutical

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