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Ref:HR/PU-04-2022- 207 Share/Bookmark

 

SQUARE Pharmaceuticals Limited, the flagship company of SQUARE Group and certified by major international pharmaceutical regulatory authorities, is holding the 1st position in the pharmaceutical industry among all national and multinational companies of Bangladesh since 1985. SQUARE Pharmaceuticals Limited has become a global player starting its operation in Kenya. Right now we are looking for smart, energetic and result oriented team members, who will share with us our pride and support our continuous growth. If you think you have what it takes to be a member of SQUARE, do not wait to apply as:

Executive, Quality Control/Quality Assurance/ Validation

Application Deadline:
Saturday, April 30, 2022

Job Status : Full Time
Work Station : Patikabari, Hemayetpur, Pabna
     

Major Duties and responsibilities:

  • For Quality Control:
    • Organize and carryout analytical activities of raw materials, packaging materials & finished products
    • Prepare specification, test procedure and analytical test report of bulk products
    • Prepare & maintain working standard
    • Review & update analytical test method of bulk products
    • Prepare & store volumetric solution, test solution & reference solution
    • Maintain all compliance related laboratory activities & documentation
    For Quality Assurance:
    • Monitor dispensing of raw materials as well as manufacturing & packaging processes in compliance with GMP
    • Perform IPC, BMR-BPR checking, change control activities and batch release activities
    • Prepare and control of SOPs and ensure QMS related documentation
    • Handle the Market Compliant, Deviation, QIR, CAPA, NCR & rejections
    • Handle the Batch document & Retention Sample and ensure proper investigation of quality incidents
    • Perform Training Needs Assessments (TNA) to prepare & conduct training programs of employees
    For Validation:
    • Conduct and ensure the qualification of new system and re-qualification of existing system, equipment and instrument according to validation master plan schedule
    • Prepare & implement the validation related Standard Operating Procedures (SOP) and protocols
    • Organize and carry out microbiological analysis of raw materials, finished products, water & environmental samples
    • Ensure preservation & maintenance of control microorganisms & other laboratory reagent
    • Ensure preservative efficacy test in different formulations, validation of sterilization, depyrogenation and aseptic operation
    • Maintain documentation, development and up gradation of test formats & record keeping


Pre-requisite to apply:
  • M. Pharm or M. Sc. in Chemistry/Applied Chemistry/Biochemistry (From reputed Universities)
  • 1-2 years of related experience is preferable but fresh candidates are also encouraged to apply
  • Well conversant in MS Office
  • Good interpersonal and communication skills
  • Capable to work in a team and in shifting environment
  • Within 30 years of age
     
Salary Range : An attractive remuneration package will be offered

Only short-listed candidates will be called for further selection process and hard copy of CV will not be entertained.

SQUARE STRONGLY DISCOURAGES SMOKERS TO APPLY

 

Applied Date Expired!
This is not a valid vacancy that you select or may be the vacancy already expire to apply. If you come this page through bookmark please delete your bookmark. This link is not no more valid link. We recommand you to visit our home page and browse our available job(s) (if any).

 

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