Executive/Sr.Executive - Quality Control (QC)

Job Description

Title: Executive/Sr.Executive - Quality Control (QC)

Company Name: SHINIL Pharma Ltd. (Sister Concern of SHINIL Group)

Vacancy: 03

Age: 28 to 40 years

Job Location: Gazipur

Salary: Negotiable

Experience:

  • 2 to 4 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Animal/Plant Breeding
  • Freshers are also encouraged to apply.


Published: 2025-10-26

Application Deadline: 2025-11-15

Education:
    • Master of Science (MSc) in Chemistry
    • Master of Pharmacy (M.Pharm)


Requirements:
  • 2 to 4 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Animal/Plant Breeding
  • Freshers are also encouraged to apply.


Skills Required: Pharmaceuticals

Additional Requirements:
  • Age 28 to 40 years
  • Good interpersoanl skills to collaborate with cross-functional team

  • Proficiency in MS Office applications.



Responsibilities & Context:
  • Prepare daily work schedule & Instruct subordinates to start work accordingly. Analysis of product, raw materials, packaging materials and water and reporting.

  • Monitoring of subordinates to perform analysis / testing of raw materials, bulk materials, intermediates, finished products, packaging materials Reduce the analysis and testing time of finished products and raw materials by developing technical methods and also prepared alternative method in a cost effective way.

  • Ensure that all identifications & testing are done correctly according to specifications and records are compiled properly. Preparation and standardization of volumetric solution and test solution.

  • Ensure that all test solution, volumetric solution, buffers and indicators are controlled and labeled time to time.

  • Ensure that all Equipment`s are calibrated & all Operations in QC Laboratory according to GMP including GLP.

  • Ensure that all reference samples of RM & Finished Products are kept as scheduled and records are maintained properly.

  • Ensure that all Reference Standard and working standard are kept properly and records are also maintained .

  • Prepare monthly requirement of Reagents, Laboratory, Glassware and Consumables.

  • Ensure all retention samples of raw material and finished products are kept as scheduled and records are maintained properly.

  • Provide guidance to subordinate to prepare SOP, Specification and standard test procedure of Raw Material ,Packaging Material & Finished product.

  • Check and review departmental standard operating procedures and other documents.

  • Assist Product Development personnel in development of test method of RM, FP and its Validation.

  • Ensure QC area is kept neat & clean condition and the equipment`s are maintained properly.

  • Any other assignment given by Plan management.



Job Other Benifits:
  • Mobile bill,T/A,Weekly 2 holidays
  • Lunch Facilities: Full Subsidize
  • Salary Review: Yearly
  • Festival Bonus: 2
  • As per company practice



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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