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Ref:HR/DU-09-21-191 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, and is now on its way to become a high performance global player by starting the operation of state-of-the-art pharmaceutical manufacturing plant 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:

Associate Scientist, R&D / Executive, Regulatory Affairs (Global)

Application Deadline:
Saturday, September 25, 2021

Job Status : Full Time
Work Station : Kaliakoir Plant, Gazipur
     

Major Duties and responsibilities:

  • For Research & Development
    • Conduct formulation activities for new & existing products and pre-formulation study for method development
    • Perform analytical method development for both compendia & non-compendia method
    • Ensure the trouble-shooting activities by maintaining compliance with quality
    • Raise Document initiating form Change Control Report, Change Document Report, Handling of Deviation and perform risk assessment as per requirement
    • Prepare Process Optimization (PO), Process Validation (PV) documents like protocol, batch documents etc. and conduct the PO and PV Batches as per procedural requirement
    • Analysis of stability sample for new products as per schedule
    • Conduct analytical method validation and verification for new products
    • Conduct operation of HPLC, GC, UV-VIS spectrophotometer & Atomic spectrophotometer
    • Compile analytical documentation with maintaining GDP
    • Perform cleaning validation activities as per regulatory requirements
    For Regulatory Affairs
    • Prepare CTD (Common Technical Documents) /ACTD (ASEAN Common Technical Documents) and dossiers for export markets
    • Provide updated regulatory information to respective concerns and follow up the implementation
    • Review and prepare technical documents associated with CTD / ACTD preparation
    • Respond to different queries raised by different regulatory authority associated with dossier evaluation or facility inspection
    • Prepare Annexure/Recipes and arrange Drug Testing Laboratories (DTL) samples as per requirement
    • Check the newly developed artwork with annexure for both local & export markets
    • Maintain liaison with different departments & provide feedback regarding inclusion materials for new products


Pre-requisite to apply:
  • M. Pharm / B.Pharm / M. Sc in Chemistry or Applied Chemistry or Bio-Chemistry & Molecular Biology (from public or reputed private University)
  • 2-3 years’ relevant experience is mandatory
  • Good interpersonal and communication skills
  • Candidate must possess excellent planning & execution skills as well as strong quantitative & qualitative analytical skills
  • Well conversant with MS Office
  • Within 32 years of age
     
Salary Range : Attractive remuneration package will be offered

Only short-listed candidates will be called for further hiring 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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