Full-Time

Senior Regulatory Affairs Specialist

Direct Staffing

Direct Staffing

No salary listed

Santa Clara, CA, USA

In Person

Category
Legal & Compliance (2)
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Requirements
  • Experience in global regulatory affairs in in vitro diagnostics, medical devices, or pharmaceuticals with a history of successful regulatory submissions, including 510(k) submissions and premarket approval approvals in the United States and Asia.
  • Experience leading company-sponsored interactions with regulatory bodies, especially the U.S. Food and Drug Administration.
  • Excellent oral and written communication skills.
  • Bachelor's degree or Master's degree or equivalent; typically 8+ years of relevant experience for this level.
  • Regulatory strategy development and providing regulatory assessments and plans for international product registrations and approvals.
  • Regulatory submissions and reporting in accordance with company goals, regulatory requirements, and partnership contracts.
  • Ability to interact and collaborate with pharmaceutical partners and represent Regulatory Affairs on project teams.
  • Stays abreast of global in vitro diagnostics regulations and guidances, especially Companion Diagnostics.
Responsibilities
  • Provide expertise in regulatory affairs leading to successful regulatory registrations and approvals of Companion Diagnostic products in global markets.
  • With Regulatory Senior Management, develop regulatory strategies related to Companion Diagnostics product development.
  • Provide regulatory assessments and plans for international product registrations and approvals.
  • Interact and collaborate with pharmaceutical partners in joint meetings.
  • Ensure accurate and timely preparation of regulatory submissions and reporting in accordance with company goals, regulatory requirements and partnership contracts.
  • Work across the organization to ensure alignment of regulatory processes, standards and compliance; provide expertise and advice in obtaining Companion Diagnostics product registrations and approvals in the Pacific Asian market.
  • Represent the Company in third-party meetings, especially with FDA, and regulatory associations.
  • Stay abreast of global in vitro diagnostics regulations and guidances relevant to Companion Diagnostics.
Desired Qualifications
  • Experience in Companion Diagnostics.

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