: 1.Drug related Conduct of clinical studies, data collection, statistical analysis, report writing Keeping track of changing legislation in regions where the company distributes its products. collect, collate and evaluate scientific data from a range of sources. To give strategic and technical advice to R&D, production, QC department, etc right from the beginning of the development of the product, making an important contribution both commercially and scientifically to the success of a development program and a company as a whole. advise scientists and manufacturers on regulatory requirements.
2.Business Development country to country for our product export.
Qualification
: A Bachelor's degree in the field of science especially pharmacy, biology, pharmacology, microbiology, biochemistry. Ability to keep up to date on current regulations.Diploma /Certificate course in Clinical Trial.
Experience:
For experience more than 5 years in position of Drug Regulatory Affairs.Fresher not applicable.Large Volume Products Dry Powder Products handling preferable.
Location
: Kolkata (West Bengal),
Salary
- negotiable.
Job Type: Walk-In
Pay: ₹15,000.00 - ₹40,000.00 per month
Work Location: In person
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