микрорайон Коктем-1
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The Regulatory Affairs Senior Associate is responsible for implementing regulatory strategies and submissions in support of new and existing products in CCAR region;
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Perform regulatory processes and work independently on each step:
•Documents Request from manufactures
•Registration Dossier Preparation
•Cooperation with local business
•Cooperation with consulting and translation agencies
•Submission documents
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Maintain and update verified regulatory system
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Review Promotional materials
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Ensure proper communication with the authorities
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Support development of artworks
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Be accountable for business requests and needs
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Responsible for the timely completion of regulatory projects and submission of documentation to regulatory agencies;
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Assist the Local cross-functional team and Global Regulatory team in analyzing CCAR product data, Regulatory legislation and providing CCAR specific information;
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Order registration samples and reference standard
- High Medical, Pharmaceutical, Chemical, Biological Education
- 3 year and more experience in Regulatory Affairs
- Profound user knowledge of all standard IS applications (MS-Office etc).
- Competitive salary;
- Life and medical insurance;
- Hybrid work format;
- Annual bonus.