Sunday, March 1, 2015

Eskayef Bangladesh Ltd.

Job Description / Responsibility
  • Pre-formulation study of new drug products,
  • Design & execution of prototype batches for new drug products,
  • Manufacturing of scale up batches & launching of new drug products into market
  • To prepare Product Development Report
  • Job Site/ Location: Eskayef Bangladesh Ltd., 400 Squibb Road, Tongi Industrial Area, Tongi, Gazipur


Job Nature
Full-time

Educational Requirements
  • The person we are looking for would have a graduation/post-graduation in Pharmacy from a top tier institution.
  • Additional Job Requirements
  • Creative thinking, numerical skills, excellent interpersonal skills and a natural ability to communicate effectively.
  • Candidate having 1 to 2 years experience In formulation development will get preference.

Job Location
Gazipur

Other Benefits
  • Attractive package at the top of the industry
  • A supportive environment with world-class training & international exposure to bring out the best in our people
  • Excellent work culture, team spirit & performance recognition schemes
  • Rapid career advancement and personal development for al high potential individuals

Apply Instruction
If you think you are the person we are looking for, please mail your resume with a recent passport size photograph to the following email address: career@skf.transcombd.com & subject your e-mail as Development Pharmacist.
Candidates who applied earlier NEED NOT TO APPLY.

Application Deadline: Mar 14, 2015

Company Information

Eskayef Bangladesh Ltd.
Business : Eskayef Bangladesh Limited one of the fastest growing top-of-the-line pharmaceutical companies in Bangladesh, is engaged in the manufacture and marketing of a wide range of therapeutic drugs, bulk pellets and animal health & nutrition products to satisfy unmet medical needs and improve people
s quality of life. True to its vision of offering world-class healthcare products, Eskayef has undertaken a new project to expand its state-of-the-art pharmaceutical operations under the exclusive technical supervision of one of the leading European pharmaceutical consultants. The new facility is being designed to conform to European CGMP with particular emphasis on meeting MHRA standards of the UK in order to facilitate exports to overseas markets.

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