Designation Drugs Regularity Executive Candidates Having The Central Drugs Standard Control Organization(CDSCO) experience and similar with these organizations can apply. Informing strategic regulatory controls and providing the worldwide regulatory policy for product development, manufacturing, and registration: It aids the applicant in advancing a universally accepted product. compiling comprehensive dossiers, and reviewing technical documents such as AMV, MFR, PVPR, BMR, STS, STP, COA, stability reports, protocols, and API documents. Seeking a challenging role to leverage this experience and drive regulatory excellence. Form 8, Form 12, Form 16, Form 19, Form 40 & Form 42 Form CT-04, CT-16 & CT-18 Form MD-14, MD-16, MD-22, MD-24, MD-26 & MD-28 Preparation of Informed Consent Documents Preparation & Submission of Post approved and various applications on SUGAM portal To complete record data of the company's products and maintain the records of therapeutic products in agreement with current regulations and guidelines. To prepare data about a new product for doctors and other healthcare professionals for harmless and effective practice of medicine and maintain records, and reports of post-marketing surveillance of the new product. It also helps to prepare the leaflets and advertising material for existing as well as new drugs. Documentation for Italy, Brazil,Belgium,USA. Required Expertise: Stability Data , Process Validation, Pharmacovigilance, Device Master File Job Types: Full-time, Regular / Permanent Experience:4-6 No Fresher candidate candidate will be preferred, For your kind review, kindly find the approved terms attached. Thanks & Regards AJAY BABU BOJJA SENIOR Talent Acquisition Executive Mobile & WhatsApp: +91- 9966723725 Email: [HIDDEN TEXT]