Sentiss Pharma require Scientist in Formulation Development

Incorporated in 1990, Sentiss is committed to providing the best quality pharmaceutical products primarily in the Ophthalmic, ENT and Inhalation segments. Over the past 25 years, by exhibiting commitment and showcasing our winning culture, Sentiss has evolved tremendously and is recognized as the third best Ophthalmic Company (IMS 2015) in Russia. Sentiss’ footprint on the world map is a testimony to its quality philosophy and practice of product differentiation. Sentiss strives to be a global leader in its core segment and continues to expand its operations in Russia, CIS, Europe, USA and Indian markets. Sentiss has a quality workforce of 700+ people across multiple geographies. Sentiss is recognized as one of the Top 100 Great Places to Work in India in 2015. Since its inception in 1990, we have been continuously evolving and has crossed several milestones during this journey. Sentiss Research Centre (SRC) filed 50 patent applications out of which 9 patents have been granted till end of Q2 2016.

Post : Research Scientist / Sr. Research Scientist - Formulation Development

Job Description
Project initiation activities:-

• To perform literature search required for idea generation form (IGF) upon receiving IGF
• To review DMF received from suppliers
• To prepare product feasibility based on IGF received
• To create the item codes for material and procure material and Reference Listed Drug (RLD)
• To assist AD lab for Q1 Q2 estimation of RLD
• To draft tentative specification for API, RM and finished good
• To plan laboratory trials and stability batches
• To finalize proposed manufacturing process
• To initiate filter validation process with the filter supplier

Documentation:-

• To prepare tech transfer documents including MFR, BOM, Process flowchart, Critical process parameters and critical quality activities
• To review product specifications, manufacturing documents
• To prepare documents for trial batches
• To prepare product development report
• To prepare and review SOPs and prepare response for internal audits
• To review documents related to filter validation
• Product Specification/ Tech Transfer/ Commercialization
• To organize and execute trial pre exhibit and exhibit batches at plant
• To execute first three commercial batches at plant
• To provide technical support for existing commercial batch
• To perform investigation of failures during exhibit batches/ stability (Out of Specification)
• Innovation
• As a stretch target come up with innovative and patentable formulations proposals or novel ideas which can reduce workload or expenses

Additional Information
Experience : 3 - 7 Years
Qualification : M.Pharm
Location : Gurgaon
Salary: INR 4,00,000 - 9,00,000 P.A
Industry Type : Pharma
Functional Area : R&D
End Date : 25th June, 2018