- Responsible for the preparation of moderately complex regulatory submissions which require interaction with departments outside of Regulatory Affairs CMC for investigational products for US, Asia and LATAM and marketed products for US in line with ICH requirements, regional requirements and scientific and company policies and procedures.
- Responsible for routine clinical and commercial labeling approvals and changes, protocol reviews, drug listing review and ensure ensuring product packaging and associated information is updated and maintained in accordance with the product license.
- Develop and maintain knowledge of regulatory requirements independently and with line manager.
- Assess change controls for regional regulatory impact and record assessment using a variety of internal systems.
- Contribute to local process improvements, which have an impact on the working of the RA CMC function or other departments.
- Primarily plans, schedules and arranges own activities in alignment with project goals and deadlines.
- Must be capable of leading a small team in preparation of regional submissions.
- Bachelor's Degree with a minimum of 6+ years of relevant training or industry experience preferably in a GMP environment, OR a Master's Degree with a minimum of 4+ years of relevant training or industry experience preferably in a GMP environment.
- Degree in a relevant scientific field.
- Relevant Regulatory CMC submission experience.
- Regulatory Affairs Certification (RAC).
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Regulatory Affairs CMC Associate - San Mateo, United States - The Fountain Group
Description
Overview:
Prefers the candidate to be local in the Bay Area BUT will consider qualified candidates with Pharma Regulatory CMC experience in the Pacific time zone ONLY.
Responsibilities
Required
Duration: 12+ months
