HomeRegulatory AffairsFormulation Development (RA) | Europe - Injectables | Alembic Pharmaceuticals | Vadodara

Formulation Development (RA) | Europe – Injectables | Alembic Pharmaceuticals | Vadodara


Alembic Pharmaceuticals Limited, with an established presence in the Indian pharma industry, has a proud, historical track record going back one hundred years. With a turnover in excess of Rs. 3000 crores today, Alembic Pharmaceuticals Limited is one of the leading API & Formulations manufacturing and marketing pharmaceutical company. We continue to enjoy leadership positions in antibiotics, anti-infective, anti-cough, and also have a significant worldwide presence in specialty therapeutic areas such as cardiology, neurology, diabetology, etc.

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We have newly setup plants of Oncology, General Injectable, and Dermaceuticals. Upcoming plans of General Oral Solid Dosage at Jarad, near Vadodara. Alembic is having manufacturing facilities at Vadodara, Panelav, Karkhadi, Jarod in Gujarat, and Domestic manufacturing of Formulations at Sikkim. Gujarat based facilities are approved by the US FDA, EDQM, TGA, MHRA, and MCC. Alembic Research Center at Vadodara (ARC) and AG Research Center at Hyderabad a world-class research organization provides a comprehensive range of services in the areas of synthetic chemistry, formulations, NDDS, Oncology as also preclinical pharmacology, bioequivalence / bio-analytical studies, etc. ARC & AG Research, designed to state-of-the-art GLP standards with more than 350 scientists working on the latest technology and systems. Our current employee strength is in excess of 8000 across the country. A continuously expanding organization, we invite dynamic, result-oriented competent personnel to join us across various functions

Position: Formulation Development-Europe-Injectable (RA)

Location: Vadodara

Job Description:

  • Managing and evaluating injectable products for an extension to Ex-US markets like Europe, Canada, and Australia.
  • Preparation of Dossier extension forms, specifications, Master formula records. Managing change controls for extending products to Ex-US markets.
  • Preparation of product development reports for Ex-US market products. Supporting regulatory and other cross-function teams for filing of Ex-US market products.

Qualification: M.Pharma

Experience: 1-6 Years

Salary: Negotiable

Contact Details:

talent@alembic.co.in,  corporate@alembic.co.in

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