Caplin point Laboratories WE’RE HIRING!!!:
Responsibilities: > To prepare IP/Patent landscape & IP/Patent clearance report for parenteral, ophthalmic & solid oral products
> To prepare IP evaluation Report for Regulatory markets like USA, Canada, Latin American markets and to provide formulation suggestion to developmental team
> To perform FTO/infringement analysis and to assist in preparing Infringement/non infringement strategies for all developmental projects
> To evaluate all API’s characteristics (polymorph, particle size, purity profile etc.,) for all developmental products for all dosage forms
Send your CV’s to email@example.com Only shortlisted candidates will be contacted for an Interview (Skype /Zoom)
Caplin Point selected on Forbes Asia’s “200 Best Under a Billion
for 3 consecutive years (2014, 2015, 2016). US-FDA, EU-GMP, ANVISA & INVIMA approved Sterile Liquid Injectable Facility.
Caplin Point holds 2200 product licenses across Latin America & Africa, with another 400 in the pipeline.