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RA_Regulatory Affairs Specialist_Taipei

TaipeiMedtronic


  • To manage the government approval activities such as manufacturing site registration and product registration to facilitate and ensure smooth and timely introduction of new products according to business needs.
  • To cultivate close relationships with government agencies as needed in order to influence and respond proactively to the development of laws and regulations governing manufacturing site registration, product registration, post market surveillance, etc.
  • To develop, in coordination with Regulatory Affairs Manager, effective strategies to cope with issues related to manufacturing site registration and product registration.
  • To ensure the organizational operation is in compliance with corporate policies and local regulations for Pharmaceutical Affairs Act and ISO13485 related requirements.
  • To manage the government approval activities such as manufacturing site registration and product registration to facilitate and ensure smooth and timely introduction of new products according to business needs.
  • To cultivate close relationships with government agencies as needed in order to influence and respond proactively to the development of laws and regulations governing manufacturing site registration, product registration, post market surveillance, etc.
  • To develop, in coordination with Regulatory Affairs Manager, effective strategies to cope with issues related to manufacturing site registration and product registration.
  • To ensure the organizational operation is in compliance with corporate policies and local regulations for Pharmaceutical Affairs Act and ISO13485 related requirements.

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