Sr. Executive - Asst. Manager, Quality Control

Job Description

Title: Sr. Executive - Asst. Manager, Quality Control

Company Name: Everest Pharmaceuticals Ltd.

Vacancy: --

Age: 28 to 36 years

Job Location: Narayanganj

Salary: Negotiable

Experience:

  • 4 to 8 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies


Published: 2025-11-19

Application Deadline: 2025-12-15

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


Requirements:
  • 4 to 8 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies


Skills Required: Quality Control

Additional Requirements:
  • Age 28 to 36 years
  • Good communication & presentation skill

  • Experience in working for highly regulated pharmaceutical market

  • Knowledge on GMP, GLP, QMS, Calibration

  • Proficiency in MS Office applications

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

  • Familiar with CDS Server system/LIMS



Responsibilities & Context:
  • Perform/Review routine analysis of RM, Intermediate, Finished Product, Packaging Material and reviewing analytical data with proper compliance.

  • Conduct/Supervise of Analytical Method validation, cleaning validation, real time stability study, Hold Time Study etc.

  • Conduct/Ensure qualification and calibration of quality control lab equipment.

  • Handle/Troubleshoot all quality control related equipment.

  • Prepare/review SOP, STP specification, stability protocol.

  • Supervise the management of working standard, CRS, VS, Reagent.

  • Specification settings and impurity evaluation of raw material and finished products.

  • Participate in different Qualification & validation activity as required.

  • Participate in OOS, OOT, incident Investigation.

  • Participate in vendor approval Activity.

  • Perform and compile training activity in QC department.

  • 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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