Abbott

Responsible and accountable for the oversight of quality operations and GMP compliance across the TPMs under responsibility of EPD Biosimilars Operations in India.

Plans, assigns and directs the Sales Managers to achieve top line and profitability in their respective Zones. Conducts performance evaluations and takes corrective action when deemed appropriate to do so.

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.