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
Senior Regulatory Affairs Specialist in summit at Unknown Company
This position is listed as full time and onsite.