Role Summary /Key Responsibilities DMF compilation and submission to global markets Handling post approval submission and CIP assessments Submission of DMF amendment & response to Health Authority queries Providing customer support Evaluating change control assessment Providing Regulatory input for New molecule development activities Maintaining Regulatory data base Qualification: M.Sc./ M. Pharm Exp: 10 years - 16 years
Job Title
Regulatory Affairs Specialist-API