About the Company :
The company established in 1988, and more than 180 OTC products and have head quarters in Canada with the bio similar in Canada. The firm is generic based product and is scope in cosmetic beauty, personal care and is one of the fastest growing pharmaceutical company. The firm have highly talented colleagues, capability in producing new products launch.
About the Job
Department : Regulatory affairs
Location of Interview : JAMP India pharmaceuticals, A-1207, 12th Floor, Navratna corporate park, Ambi Bopal road, Ahmedabad - 380058
Qualification : B. Pharma / M. Pharma
Date of Walk-in : 7th August 22
Requirement : Candidates with experience in regulatory required to apply, Required to have experience in OSD/ Semi solid/ Injectable and Ophthalmic dosage forms.
For Assistant manager : Experience required : 6-12 years
Required exposure in Complication, review of Quality dossier in CTD format for new generic drug submission and guidance, templates
Required to see the overall summary of module-1 and 3 for all planned submissions
Need to work closely with Cross functional teams and required to maintain good collaboration with cross functional teams.
For Executive and Sr, Executive
Experience : 2-6 years
Role :
Candidate required to compile and review the dossier for new drug submissions and need to perform the post approval activities for the given product portfolio
Required to maintain mutual agreement with the cross functional teams and stake holders
Candidates unable to attend the interview could send their resumes to [email protected]
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