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Teva Pharmaceuticals is hiring for Regulatory Affairs Professionals having 04 to 08 years experience – EU Post approvals who can fulfill the following criteria.

Job location: Navi Mumbai Seawoods

Years of experience required: 4 – 8 Years

Roles & Responsibilities:

Prepare, compile, review and submit high quality submissions for all required post-approval activities in accordance with EU legislation and in-house standards. Responsibility for MA compliance with both legislation and business needs.

Prioritize, plan and monitor submission for allocated procedures while documenting and informing involved parties of progress. To give regulatory support to project teams, stake

holders and European Units for defined product

responsibilities.

Support the development and implementation of regulatory strategies for defined projects. Communicate with other Teva departments across

Europe and European Agencies regarding proposed and pending submissions.

Maintain and develop awareness of current/pending regulatory legislation and guidelines. Support the defined processes within the department and provide input where improvements can be made

Application Process –

If your profile matches the above requirement, please share your updated resume to pranita.padte@teva.co.in with subject line as “EU post approvals”

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