Teva Pharmaceuticals Hirirng Regulatory Affairs Associate I MPharm/ BPharm / MSc Apply Now
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.
DL management activity, maintenance of various databases etc.
Qualification : MPharm/ BPharm / MSc
Experience : 3-4 Yrs in relevant EU Market
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