Abbott

Analytical Method Transfer of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray. Analytical method development and validation for pharmaceutical dosage forms.

To lead and manage all regulatory affairs activities at the manufacturing site located at Mumbai and LL locations, ensuring timely regulatory submissions, compliance with regulations, and providing strategic support to institutional and international business operations.

Effectively coordinate with other functional areas within organization e.g. Medical, Training, Promo team, Supply Chain, Finance etc.

Abbott is hiring an Executive – Quality Assurance in Baddi. B.Pharma/M.Pharma with experience in solid dosage hormone manufacturing & packaging can apply.

B.Sc. / B.Pharma.; Territory Business Manager - General Medicine-Pune; Fresher with good communication skills and analytical

Regulatory Affairs Specialist is responsible for ensuring that medical devices comply with all applicable regulations in India and international markets

Ensure that the required initial and continuing training of department personnel is carried out and adapted according to need.

Achieve Division wise primary target and ensure it to be equal to or greater than Secondary. Generate maximum prescriptions & increase market share. Ensure zero cases of expiry on Stockist shelf by timely liquidation of stocks by prescription generation.

Provide technical inputs on review of CMC data for Central CDSCO and State dossiers related to new products under development Liaison with other departments such as l&D, Quality, Supply chain, Project Management, etc to deliver high quality dossiers, in accordance with business priorities