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A degree in Life Sciences, Nursing, Pharmacy, Regulatory Affairs, or Chemistry (or equivalent experience that tells a similar story)

Develop and maintain QMS for Medical Device clients; Develop regulatory strategies, submissions and compliance activities for Medical Devices clients; Control, prepare, track and archive quality and regulatory documentation for MD clients

A Graduate / Post graduate degree in Chemistry, Biology, Pharmacy, Health Sciences or similar. Project Management would be additional advantage.

Candidates must have exposure of working in a USFDA approved regulatory units

Eris Therapeutics Limited is fast growing pharmaceutical company (A Subsidiary of Eris lifesciences Limited).

Bachelors degree in pharmacy or similar medical education. Pharma experience with regulatory focus in a multi-national. Regulatory Affairs Manager, you will play a critical role in ensuring patients continue to have access to innovative healthcare solutions. Boehringer Ingelheim

As the Experienced professional in the Regulatory Affairs Sub-Function, possesses well developed skills in directing development of product registration submission, progress reports, supplements, amendments, or periodic experience reports. 

Your day to day interaction is with peers within Accenture before updating supervisors. In this role you may have limited exposure with clients and/or Accenture management.

Uses external and internal insights to identify emerging trends and requirements and to inform, develop, and refine GSC and Lilly regulatory writing, content and study submission strategies