[SK케미칼] Pharma사업 의약품 RA(허가) 담당자 경력 모집
Core
Establishing pharmaceutical approval strategies and managing regulatory affairs for drug licensing and post-approval management.
Role type
Regulatory Affairs Specialist (Pharmaceutical Licensing)
Builds
Drug licensing applications and regulatory compliance documentation for domestic and international markets.
Domain
Pharmaceuticals / Regulatory Affairs
Deliverable
client delivery
Required skills
Regulatory strategy formulation, post-approval management (renewal, changes, foreign facility registration), regulatory change monitoring, regulatory compliance review, interaction with regulatory authorities (MFDS)
Preferred skills
None stated
Technologies
None stated
Responsibilities
Formulating drug approval strategies, managing post-approval regulatory tasks, monitoring domestic and international regulatory changes, reviewing licensing regulations, handling interactions with regulatory authorities
Seniority
Entry-level to Junior (1+ years experience required)
