Regulatory Affairs Associate I - 1434
Date: Apr 5, 2021
Location: Navi Mumbai, IN, 400706
Company: Teva Pharmaceuticals
Company Info
Job Description
- 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.
- Ensure approvals are secured within the stipulated timelines for designated projects.
- Maintain registration documentation and associated electronic databases, in line with in-house procedures.
- Provide regulatory support and product information for all internal and external customers, stakeholders and TEVA project teams.
- Prioritise, plan and monitor submissions for allocated procedures while documenting and informing involved parties of progress.
- 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.
- Fulfilling other allocated department duties and ad-hoc needs at the direction of Senior Regulatory Affairs personnel.
Qualifications
Degree in science/life sciences/pharmacy or equivalent qualification(s)
Function
Sub Function
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