Job for Ph.D, M.Pharm in Formulation Development, Medicinal Chemistry Department at Amneal Pharma

Amneal Pharmaceuticals, Inc. is a global pharmaceutical company. Our team of 7,500+colleagues helps make healthy possible through the development, manufacturing, and distribution of a diverse portfolio of 270+ high-quality medicines.

Looking for candidates with relevant experience as mentioned below

<< Formulation Development (NCE) >>
Post : AGM / DGM

Experience : 12-18 years

Qualification : Ph.D / M.Pharm

Required skills :
• Lead and manage the Formulation Development team in the development of NCE formulations from pre-clinical to commercial stage.
• Define and implement the formulation development strategy, aligning with the broader RAD and business objectives.
• Lead the preparation of development reports, protocols, and documentation required for regulatory submissions.
• Identify and implement cutting-edge formulation technologies for new drug delivery systems.
• Collaborate with cross-functional teams (e.g., Analytical Development, Regulatory Affairs, Manufacturing, Clinical, and Marketing! to ensure smooth transitionsfrom RAD to commercial production.
• Oversee the preparation of regulatory submissions, including Investigational New Drug (IND) applications, New DrugApplications (NDA), and Abbreviated New DrugApplications (ANDA).
• Ensure timely and accurate responses to regulatory queries related to formulation development

<< Medicinal Chemistry (NCE) >>
Post : Senior Executive / Assistant Manager

Experience : 01-05 Years

Qualification : Ph.D (Mandatory)

Required skills :
• Develops and advances novel molecules with a complete understanding of scientific aspect.
• Planning and implementation of novel approaches to drug discovery and development independently or in conjunction.
• Designing and synthesis of novel molecules (NCE and prodrugs: of assigned project with respective goals
• Co-ordination for IP and ccmp-chem screening (whenever applicable for designed molecules subsequent patent filing
• Co-ordination with different CROs and CMOsto ensure timely synthesis of designed compounds with real-time communication over email and weekly teleconferences.
• Actively troubleshooting the challenges faced during synthesis and development of lead molecules to fast-track pre-clinical drug discovery and regulator; submissions.
• Co-ordination with pharmacology/DMPK team members for further screening of key molecules for advancement of project with data interpretation.
• Compound data & library' management and shipment co-ordination on routine basis.
• Well verse with CADD.

Job Location : Ahmedabad