Regulatory Affairs Specialist (12 Months Contract)

Stryker

  • Taipei City
  • Permanent
  • Full-time
  • 30 days ago
Work Flexibility: HybridWhat you will be doing:
  • Identifies information sources and resources for local, regional, and global regulations
  • Collects, organizes, and maintains files on local, regional, and global regulatory intelligence and other related information
  • Monitors the regulatory environment (specific regulations, guidance and other relevant information by product types, geography, etc.)
  • Provides information used to evaluate proposed products for regulatory classification and jurisdiction
  • Researches requirements (local, national, international), applicable guidance and standards and options for regulatory submissions, approval pathways, and compliance activities
  • Assists in the development of regulatory procedures and SOPs
  • Collects and organizes information on requirements for regulatory, quality, preclinical, and clinical data to meet applicable regulations
  • Organizes materials from preclinical and clinical studies for review and assists in the review process
  • Compiles and organizes materials for pre-submission reports and communications
  • Assists in the preparation of dossiers and pre-submission and submission packages for regulatory agencies
  • Tracks the status of applications under regulatory review and provides updates to the regulatory team
  • Maintains logs of communication and outcomes with regulators and other relevant internal or external stakeholders
  • Assists in the scheduling of meetings with internal stakeholders and regulators and develops and organizes materials for these meetings
Who are we looking for:
  • BS in Engineering, Science, or related degree; or MS in Regulatory Science
  • 0+ yrs experience
  • Time management skills, writing, coordination, and execution of basic regulatory items
  • Coordinate and support technical and scientific regulatory activities
  • Under supervision, performs work that is varied and that may be somewhat difficult in character, but usually involves limited responsibility
  • Some evaluation, originality or ingenuity is required
  • Clearly conveys information to peers, supervisors, and other stakeholders
  • Assists in the preparation for meetings with regulatory agencies and other stakeholders
  • Assists in the preparation of briefings and other information documents
  • Communicates information on regulatory requirements to other departments and business units
  • Composes routine communications with regulators and other key stakeholders
  • Creates clarity and direction amid complexity and develops solutions for self, colleagues, and the organization
  • Seeks out diverse ideas, opinions, and insights, and applies them in the workplace
  • Connects and relates well with people who think and act differently than oneself
  • Embraces scrutiny and accepts feedback as opportunity to learn and improve
Travel Percentage: 0%

Stryker

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