Executive - Group Manager, Product Development (Analytical)

Job Description

Title: Executive - Group Manager, Product Development (Analytical)

Company Name: Everest Pharmaceuticals Ltd.

Vacancy: --

Age: At most 30 years

Job Location: Narayanganj

Salary: Negotiable

Experience:

  • 2 to 6 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies


Published: 2025-12-04

Application Deadline: 2025-12-27

Education:
    • Master of Pharmacy (M.Pharm)
    • Master of Science (MSc) in Chemistry
    • Master of Science (MSc) in Applied Chemistry
    • Master of Science (MSc) in Biochemistry
    • Master of Science (MSc) in Biotechnology
    • Master of Science (MSc) in Genetic Engineering
  • Master of Pharmacy (M. Pharm), Master of Science (MSc) in Chemistry/Applied Chemistry/Biochemistry/Biotechnology/Genetic Engineering from Reputed University


Requirements:
  • 2 to 6 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies


Skills Required:

Additional Requirements:
  • Age At most 30 years
  • Good communication & presentation skill

  • Experience in working for highly regulated pharmaceutical market

  • Knowledge on GMP, GLP, Calibration

  • Proficiency in MS Office applications

  • Should be familiar with chromatographic software such as Lab solution, Empower 3, Chromileon 7.2.



Responsibilities & Context:
  • Analytical Method development of New Raw materials and Finished products.

  • Conduct routine analytical testing of raw material, finished product of development batches.

  • Conduct analysis of different stability samples.

  • Brand product characterization and comparative analysis with In- house formulation.

  • Perform validation/verification of analytical methods and analytical method transfer.

  • Prepare protocol and report of method validation/verification, stability study and transfer activities.

  • Handle, operate, calibrate and maintenance of all laboratory equipment and instruments.

  • Preparing SOP, STP, specification.

  • Prepare and compile documents for recipe submission to Drug Administration and sample submission to Drug Testing Laboratory.  

  • Conduct cleaning method validation activity.

  • Ensure GLP, cGMP, Safety standards, QMS and documentation compliance.



Job Other Benifits:

Employment Status: Full Time

Job Work Place: Work at office

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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