Unknown Company

Senior Regulatory Affairs Specialist

summit, nj • Posted 2 weeks ago
Onsite Full Time Management & Operations

The Senior Specialist, Regulatory Affairs will provide expertise to the organization in the development of regulatory compliance strategies and in ensuring its conformance to Health Authority requirements.

Essential Functions

  • Serve as a Regulatory Affairs subject matter expert to the Regulatory Affairs team and organization.
  • Approve, review, or prepare common technical documents (CTD) for technical content and compliance with regulatory requirements
  • Responsible for maintaining compliance with US and International Health Authority regulations for products under development and for marketed products.
  • Assist with developing and evaluating regulatory strategy
  • Keep abreast of internal and external changes, trends, and developments to the regulatory environment that may have an impact on products.
  • Author and review departmental SOPs, as well as other SOPs that may impact Regulatory Affairs.
  • Performs other special projects and duties as requested.

Education & Experience

  • Bachelor’s Degree in life sciences required with 7+ years of relevant regulatory compliance experience in pharmaceutical drug development required; or
  • Master’s Degree in life sciences required with 5+ years of relevant regulatory compliance experience in pharmaceutical drug development required.
  • Knowledge and experience with organizing responses to Regulatory Authority requests required
  • Experience with US and International Health Authority regulatory submissions preferred

Knowledge, Skills, & Abilities

  • Knowledge of FDA, ICH and other guidance documents and requirements
  • Knowledge of organizing responses to Regulatory Authority requests
  • Strong knowledge of Health Authority regulatory requirements/guidelines
  • Strong project management and computer skills (including Microsoft office)
  • Strong document management experience (hard and e-copy)
  • Ability to work with firm deadlines and adapt quickly to changing requirements and priorities
  • Strong organizational skills, written/oral communication skills and attention to detail
  • Ability to manage conflicting priorities and respond in a timely, effective manner
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Senior Regulatory Affairs Specialist in summit at Unknown Company

This position is listed as full time and onsite.

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