Dr. Reddys Lab

Support DRL sponsored or investigator initiated studies, real-world evidence generation, and post-marketing surveillance, as and when required

Responsibilities also include documentation review, maintaining product quality, coordinating training, conducting initial incident investigations, and managing process orders.

Must have broad understanding of the development of pharmaceutical products, regulatory and patent law globally. Patent and regulatory databases in different countries

Preparation and Execution of qualification protocols for Equipment's, Autoclave, Tunnel, Filling and capping machine, Lyophilizer, Washing machine, bung processor etc.

Skilled in medical device packaging and Visual inspection, with expertise in strategic planning, documentation, aligned with cGMP standards.

Responsible for discussion and planning strategies for product development, executing them and recording them in E-Lab notebook. Identify and proactively discuss potential challenges along with possible way forward.

Looking for B.Pharm, M.Pharm candidates as Product Manager to develop, implement, and maintain long-term strategies for high-potential products in our current and future portfolio, aiming to maximize market share and profitability through strategic planning and execution.

Handling the Incidents / Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical activities in Quality control laboratory.

Seeking an exceptional leader to Head Pharmacovigilance and Medical Affairs including medical information function for Dr. Reddys North America Generics and affiliates as well as Dr. Reddys Canada