Research Officer Formulation Development

Zenvision Pharma LLp

3 to 5 yrs. Navi Mumbai
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Posted on 31 Jan 2017

Job Description

Formulation development of Ophthalmic and Injectable products for regulated market-US & EU.

Responsible for literature search, patent reading and understanding.
Should have desired knowledge on regulatory requirement for US and Europe regulated market.
Responsible for taking trials in the laboratory, maintaining note book and data compilation.
Responsible for performing stability studies as per the dosage-form and regulatory requirement.
Responsible for interacting with concern analytical team member for desired sample submission and analysis planning.
Should be capable of compiling received analytical data and interpretation.
Should have hands on experience on QbD and DOE to satisfy US regulatory requirement. Responsible for developing stable formulations that meet or exceed requirements within specified timelines.

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Prashant Patil Company HR Zenvision Pharma LLp Navi Mumbai

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