Cadila Healthcare Limited
Zydus Cadila is a fully integrated, global healthcare provider, with strengths all along the pharmaceutical value chain. With a core competence in the field of healthcare, Zydus Cadila provides total healthcare solutions ranging from formulations, active pharmaceutical ingredients and animal healthcare products to wellness products. From a turnover of Rs. 250 crores in 1995, the group posted revenues of over Rs. 8600 crores in FY15. The group had posted a turnover of Rs. 4600 crores in FY 11, making it a billion dollar company. Recently, the group launched Exemptia, the world’s first biosimilar for Adalimumab, the largest selling therapy worldwide for inflammatory arthritis.
Job Title:Â Â Â Regulatory Affairs
Job Description:
Regulatory Affairs Department at Cadila Healthcare Ltd Ankleshwar API
Here is a chance to join Zydus at our API Manufacturing located at Ankleshwar as.
Key Responsibilities
1. Review and submission of DMFs to USFDA, EU and ROW countries.
2. Responding for DMF Queries received from different regulatory agencies and customers
3. Review of DMF Amendments and annual updates for drug mater files.
4. Co-ordinating with other departments to make smooth DMF filling and queries responding.
5. Review of change controls received from QA and other departments
Qualifications:Â
Education
:
UG -B.Sc – Chemistry, B.Pharma – Pharmacy
PG – MS/M.Sc(Science) – Chemistry, M.Pharma – Pharmacy
PG – MS/M.Sc(Science) – Chemistry, M.Pharma – Pharmacy
