Felix Pharma, an creative pharmaceutical company headquartered in Dublin, passionately committed to revolutionizing the landscape of veterinary care.

Felix aims to be a truly global generic companion pets’ pharmaceutical player focusing on the top 10 veterinary markets of the world.

We are looking for experienced regulatory affairs professionals for our Injectable portfolio. Candidates having experience of 10-15 years and independently doing injectable filing in the regulated market (US/EU/Canada) in a generic pharma company are ideal choice.

Candidate who can manage end to end injection facility SAP related work wrt facility DMF maintenance and can perform review and finalization of sterility assurance package from the regulatory aspect is preferred.

We are looking for experienced regulatory affairs professionals for our life cycle management role.



Candidates having experience of 10-15 years and independently doing LCM filing in the regulated market (US/EU/Canada) in a generic pharma company are ideal choice.

Candidate who can manage end to end life cycle management work like such as CBE-30, PAS and annual reports and can support in review and finalization of various LCM submissions/variation is preferred.

We are having US FDA approved plants and working with multiple FDA approved facilities across the globe for our veterinary portfolio.

Job location: Gr Noida

Pl see our approved product list here: https://animaldrugsatfda.fda.gov/adafda/views/#/home/searchResult www.Felixvet.com pl send your cv at [email protected]

📌 Regulatory Affairs Manager (Noida)
🏢 Felix Pharmaceuticals
📍 Noida