Roles and Responsibilities
Scientific development and template preparation for protocols and procedures,related to ortho implant surgeries during piloting phase as well post-marketing surveillance studies.
Provide product specific Regulatory strategies to mitigate risk; works in conjunction with production and QA team to provide advice on process and labeling changes.
Review of Development  documents,such as Development report, llG, MFR,MPR,Trade dress e1c
To assist the QA/RA team and ensure quality and good standard operating procedures within the company Worked for Regulatory requirement for different countries
Compliance with respect to internal external audits meeting regulatory/ accreditation requirements Review of filing documents such as Spec1ticat on.STP BMR. analytical method development. COA etc 

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If Interested, kindly forward your updated CV on hr5@tasolutions.in  or can call on 9023404909. We will really appreciate it if you forward this position to your colleagues or Friends.