JOB OPENING
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Regulatory Affairs Associate
2014-12-18 |
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´ã´ç¾÷¹« | [Purpose of Job] The Regulatory Affairs Associate is responsible for assisting in timely and efficiently managing drug registration process from beginning to end in accordance with regulatory requirements. [KEY Accountabilities and Responsibilities] - Assists in obtaining marketing approval from the KFDA for a planned new drug(K-NDA) and ensures subsequent maintenance of drugs registered (Supplemental & Amended K-NDA). - Contributes to the effective and efficient initiation of clinical trials with the company's investigational new drug through supporting for K-IND submission and approval. - Ensures registered products are maintained and updated in full compliance with all relevant legislation and SOPs. - Provides regulatory affairs related information to other departments. - Assists Regulatory Affairs Manager to establish, develop and maintain close working relationships with the relevant regulatory authorities and associations (KFDA, MOHW, KJPA etc.) - Assists Regulatory Affairs Manager for coordinating regulatory activities among departments (Marketing, Business Development etc.) and timely communications with TGRD, TPC and Millenium. - Assisits Regulatory Affairs Manager to develop new product registration strategy. (Essential responsibilities : 1. Registration feasibility pre-review 2. Preparation of K-NDA or K-IND files 3. DMF and/or GMP site inspection 4. Maintenance and update of registered products 5. Product label management 6. Interactions with TGRD 7. Other duties as assigned |
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°æ·Â | - 2+ years experience in pharmaceuticals with at least 2 years in RA - Must be degree qualified, pharmacy - Proven ability to build and maintain relations with internal as well as external customers - Good project management skills and effective communication skills |
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