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Abbott
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Research Scientist

Research Scientist

Abbott

0 years

0 Lacs

mumbai maharashtra india

Posted:1 day ago| Platform:

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Skills Required

research stability manufacturing development prototype documentation report maintenance calibration engineering technology schedule evaluation estimate design doe management

Work Mode

On-site

Job Type

Full Time

Job Description

Pupose:Deliver formulations in defined timeframe to meet product delivery goals for I&D
Development of different formulations either as generic or differentiated generics. To demonstrate successful stability and scale up at manufacturing site.Core Job Responsibilities

Development of formulation using scientific rationale in use of excipients to create a reproducible prototype formulation.
Ensure Proper documentation of every trial in the log note books and then using the information for creation of the Product Development Report for use in dossier for filing.
Use of QbD wherever required for Product and process optimization.
Ensure proper upkeep, maintenance and calibration of the equipment.
Ensure scale up of the developed formulation works at engineering batch level.

Key Deliverables

Literature/Patent search to create drug profile
Prototype development with rationale use of excipients
Preformulation study as may be required for formulation development
Conduct 6 months accelerated stability studies to ensure stable formulation
Proof of concept studies to demonstrate BE or comparative PK as the case may be
Scale up studies at 1/10th scale or engineering batch
Technology transfer and manufacturing of Bio/Clinical batch

Job Title: Jr Research Scientist FormulationJob Function: Innovation & DevelopmentLocation: Mumbai (Andheri MIDC)Reporting to:Sr Group Leader FormulationCritical Success Factors: Functional/ Technical: Functional / Technical:1. Formulation and Product Developmenta. Schedule and follow all the steps to deliver the drug as per QTPPb. Select the suitable polymers / excipients based on either properties or scientific rationalec. Evaluation of CQA of drug / excipients and estimate its implications for product developmentd. Designs the process which is reproducible and scalable with higher yield, cost effective, and environment friendly2. Design of Experimentsa. Executes the experiments as per DOE to optimize product and process3. Pharmaceutical Development Report (PDR)a. Prepares PDR as per Common Technical Document (CTD) module 3 requirementsb. Complies with regulatory requirements as defined in QTPP4. Project Managementa. Is able to plan and prioritize multiple project deadlines to meet product delivery goals

Education & Experience

M. Pharm/Ph. D.
5 to 7 yrs

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Research Scientist