Officer, Quality Assurance

Aug 20, 2017 12:11 am

Sun Pharmaceutical (Bangladesh) Limited Company Name: Sun Pharmaceutical (Bangladesh) Limited

Job Title: Officer, Quality Assurance

Job Type: Full Time

Number of Vacancies: 1

Job Category: Medical/Pharma

Deadline: 28 Aug,2017

Educational Qualification:
    B.Pharm/ M.Pharm/ M.Sc in Chemistry/ Applied Chemistry/ Biochemistry

 

Experience:
  • 1 to 4 year(s)
  • The applicants should have experience in the following area(s):
    Quality Controller /Assurance
  • The applicants should have experience in the following business area(s):
    Pharmaceuticals

 

Requirement:
  • Age 27 to 30 year(s)
  • Having 1-3 years experience in the similar positions in a reputed pharmaceutical company
  • Good knowledge in computer operation
  • Good communication skill both in English and Bengali
  • Good analytical skills
  • Self-management including: Ability to prioritize own work load, able to work independently, committed to meet deadlines and maintain confidentiality in all areas of work

 

Other Opportunities:
Job Location

Gazipur

Salary Range
    Negotiable
Other Benefits
    Long term benefits like PF, WPPF, Gratuity, Insurance and other benefits will be offered to the finally selected candidate according to company policies.

 

Instruction :
If you think you are the best match for the above mentioned position, please apply online or send hard copy of your updated resume with contact mobile number and a recent passport size color photograph.

Applicant must enclose his/her Photograph with CV.

Application Deadline : Aug 28, 2017
Company Information
Sun Pharmaceutical (Bangladesh) LimitedAddress : House No. 4, Road No. 16A (Near Gulshan Post Office), Gulshan-1, Dhaka-1212Web : www.sunpharma.com

 

Job Detail:

Job Description / Responsibility
To co-ordinate with manufacturing department in controlling their process and products at every stage of manufacturing to meet the established specifications through in-process checking and reporting.
Routine cGMP auditing of each area for any non-conformity, CAPA implementation and reporting.
To monitor event, market complaint, product recall and implementation of CAPA and reporting.
Preparation and control of SOP as per corporate guideline.
Execution of process validation and equipment qualification protocol.
Withdrawal, Storage, Physical Inspection, Issuance and Destruction of Control Sample of Drug Products
Final inspection and batch release of finished products.
To review documents like BMR/BPR, SOP etc. and find out any non-conformance for correction and reporting.
Handling and reporting of any rejection.