Active participation in method development, validation and subject sample analysis.
Process and analyze the subject samples as per the project requirements.
Cadila Pharmaceuticals is an Indian multinational pharmaceutical company based in Ahmedabad. The company's operations focus on manufacturing products ranging from active pharmaceutical intermediates, finished formulations, food supplements, biotechnology products and pharmaceutical machinery.
After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times. Our legacy of over 70 years in healthcare and being dedicated to life in all its dimensions is reaffirmed in our new mission, vision and purpose. Unifying ourselves under the Zydus name, Cadila Healthcare Ltd., is renamed as Zydus Lifesciences Ltd.
Post : Executive | Analytical Development Laboratory
To manage multiple site Regulatory with multiple dosage forms. To Develop strategies and ensure to comply with Regulatory Bodies. Filing strategy documents for emerging markets and active Involvement in tender Business.
lntermediate plus Finished area Adhere to Safety and CGMP Norms, Distillation, Layer Separation, Solvent Handling, SRP, Hydrogenation, Micronization, DCS Automation; URS/IQ/OQ/PQ. QMS CCP/Deviation/OOS/ OOT. Adhere to Safety and CGMP Norms
Managing the regulatory aspects of projects and products for pre-approval and post approval submissions for biological, new drugs and global and local clinical trials. In addition, participating in project team meetings, by providing regulatory support to ensure compliance with all local requirements.
Strong analytical and problem-solving skills to troubleshoot experimental issues and propose solutions to challenges. Excellent written and verbal communication skills to present findings, write reports, and collaborate with team members and other stakeholders.