R&D - Associate Regulatory Affairs Manager - BJ

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  • 北京
Internal Job Description

JOB DESCRIPTION

(Associate Regulatory Manager)

JOB PURPOSE:

 

       Be accountable for implementing regulatory strategy to obtain the regulatory approval to support various development, manufacturing, sales and marketing activities for the designated product group 

     Support line Manager for the HA interaction for the strategy discussion and be accountable for the HA interaction to facilitate the implementation process

KEY ACCOUNTABILITIES:

 

      Be accountable for implementing regulatory strategy to obtain the regulatory approval to support various development, manufacturing, sales and marketing activities for the designated product

        Lead the submission for the responsible projects or tasks with the guidance of senior regulatory manager

        Collaborate with related functiona at corporate, IA and work with affiliates to support the regulatory activities in the region

        Ensure the high-quality submission with effective communication with agency and internal stakeholders/peers for the assigned projects/tasks

      Suppoert Line Manager or Submission Team leader for the regulatory strategy assessment

        Work with related functions at GRA and China region to develop and implement the regulatory strategy of the responsible projects for the region, aligned with global strategy and regional business strategy

        Work across project team and related workstreams to evaluate, Dossier gap assessment, Regulatory pathway and timelines, RA compliance, Implication of the findings on the deal terms, Ways to mitigate identified risks, implications on cost / time etc.

        Provide the Inputs for strategic projects on RA regulations, requirements, trends

        Provide regulatory intelligence collection and analysis

      Provide Regulatory support to cross-functions to ensure business success

Ensure regulatory compliance and work in compliance way

JOB-HOLDER ENTRY REQUIREMENTS:

 

Education:

 

         Master degree or above in Pharmacy, Medical, Biology or related field (Bachelor acceptable in special cases)

 

Experience & knowledge:

       Mimimal 3 years+ RA experience along with 5 years industry working experience with track record performance in obtaining regulatory approval

Core competencies:

 

      Good computer skill in EXCEL, POWERPOINT and WORD;

      Good interpersonal communication skill

      Chinese and English (proficiency level) skill both in spoken and written