JOB DESCRIPTION OF REGULATORY AFFAIRS
TOTAL YEARS OF EXPERIENCE: 2-4 YEARS
Handling dossier, COPP submission and query Handling for South East Asian Country, East Africa, Latin America, Central America, Europe.
In depth knowledge about regulatory requirements for above region
Need to work independently
Need to have knowledge about legal documents requirement and it's processing.
New customer development and new business development from above region.
Market research on different competitive products in the market
gathering, evaluating, organizing, managing and collating information in a variety of formats
ensuring compliance with regulations set by the Medicines and Healthcare products Regulatory Agency (MHRA)
outlining requirements for artwork, labelling, storage and packaging
providing advice about regulations to manufacturers & customers, liaising and negotiating with regulatory authorities, ensuring that quality standards are met and submissions meet strict deadlines
Writing comprehensible, user-friendly, clear product information leaflets and labels.
Job Type: Full-time
Pay: ?18,000.00 - ?25,000.00 per month
Schedule:
• Day shift
Education:
• Master's (Required)
Experience:
• 5G: 2 years (Preferred)
Work Location: In person
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