Posted:1 day ago|
Platform:
Work from Office
Full Time
1) To maintain high degree of quality of documents required for submissions to get the approval without deficiency / non-critical deficiency.
2) Timely readiness and submission of documents / dossier for variation / new submissions and renewals in different countries.
3) To follow Global Working Instructions and local SOPs for new submissions, variations and renewals and also support DRA initiatives.
4) Proven expertise in scientific writing and regulatory documentation
5)Strong project management capabilities and ability to work independently
6) Familiarity with global regulatory requirements and submission processes
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Manpowergroup Services India
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