SPECIALIST VACANCY @ NOVARTIS
Job Description
Position Purpose
Ensure preparation, validation, dispatch and submission of
compliant and high quality initial, 2nd wave and maintenance Regulatory filings
according to submission plans. Update respective Regulatory systems for
Registration Management, Publishing and Document Management. Support the Global
Regulatory teams during the product development phase and provide input as
appropriate. Follow Regulatory procedures and timelines
Minimum requirements
University
or College Degree in any field or life science with relevant industry
experience or comparable degree Good communication in English (oral and
written). • At a minimum 2 years’ experience in the Pharmaceutical area,
specifically in Regulatory Operations • Experience in the Regulatory submission
publishing, area is preferred • Knowledge of Regulatory guidelines for the
areas mentioned above • Organizational awareness and experience working
cross-functionally and in global teams is a plus • Ability to work under
pressure, demonstrating initiative and flexibility • High level understanding
of Regulatory quality, standards and policies. • Attention to detail and quality
focused • Team-minded
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