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Senior Regulatory Affairs Associate

2.00 to 3.00 Years   Mumbai City   23 Nov, 2020
Job LocationMumbai City
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaCustomer Service (International),R&D / Product Design
EmploymentTypeFull-time

Job Description

Works effectively within a team environment but may work independently delivering services within their area of competence Must be able to work independently on submissions, mentor publishers and proactively takes up publishing and related activities Understanding of global regulatory submission formats, industry standards, and guidelines, software validation concepts, and publishing best practices. Responsible for compiling, publishing and QC of regulatory submissions Has previous experience of publishing high quality submissions in eCTD, NeeS and pCTD formats Understanding of global regulatory submission formats, industry standards, and guidelines, software validation concepts, and publishing best practices. Proficient in Microsoft Windows desktop and server environments; Microsoft Office products; Adobe Acrobat and plug-ins; Documentum and/or other document management systems; Parexel LIQUENT InSight and SmartDesk product lines. Employs advanced troubleshooting techniques to efficiently address publishing system and desktop tool issues. Works within broad project guidelines as directed by the project lead and/or technical SMEs Takes initiative to prioritize work to achieve specified project outcomes while confirming alignment with project lead and line manager Capitalizes on opportunities to improve one s own performance and seeks feedback from the project lead and colleagues Applies information provided by the project lead or senior colleagues to complete assigned project activities Produces quality work that meets the expectations of project lead and the clientQualificationsBachelor s degree or equivalent in technology or life sciences-related discipline,

Keyskills :
clinical trialsdocumentationapacdcgisopadobe acrobatmicrosoft officemanagement systemsdigital conversiondocument managementsoftware validationneeswindowsdesktopsoftwareadobe

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