Regulatory Affairs Manager

The regulatory affairs (RA) department of a pharmaceutical company is responsible for obtaining approval for new pharmaceutical products and ensuring that approval is maintained for as long as the company wants to keep the product on the market.

Job description

Handling the regulatory Inspections like GMP, Foreign FDA, ASEAN, Australia TGA, India, Africa, Latin America, CIS, and Middle.

Experience in filing the filling/re-registration & variation of ROW Asian, CIS &

African countries and other countries.

Required Candidate profile

Qualified professional Graduate/Diploma in Drug Regulatory Affairs with rich experience.

Excellent verbal and written communication skills.