Job Description
<Job Responsibilities> ・Manage and ensure compliance with Indonesian regulations related to: Pharmaceutical products, Active pharmaceutical ingredients (API), Medical/pharmaceutical equipment, Food and cosmetic-related products ・Handle licensing processes, including: Import permits, Distribution permits, Product registration and approval. ・Oversee and maintain compliance with CDOB (Cara Distribusi Obat yang Baik) standards. ・Act as the Person in Charge (PIC) for regulatory and pharmaceutical compliance matters ・Liaise with government authorities (e.g., BPOM, Ministry of Health) for regulatory submissions and approvals ・Support business development by advising on regulatory feasibility for new products and partnerships ・Coordinate with internal teams (sales, supply chain, compliance) to ensure smooth product flow and regulatory adherence ・Build and maintain strong relationships with Local & Multinational pharmaceutical companies ・Monitor regulatory updates and ensure company policies are aligned with the latest requirements ・Other duties as assigned.
Job Requirement
<Necessary Skill / Experience > ・Bachelor's degree ・Business English proficiency ・5 years of experience as Regulatory Affairs handling Pharmaceutical, Food, Cosmetic products from Consumer Goods Industry, has good relationship with pharmaceutical manufactures in Indonesia ・Certificated STRA (Surat Tanda Registrasi Apoteker), SIPA (Surat Izin Praktik Apoteker), CDOB (Cara Distribusi Obat yang Baik) ・Detail oriented, able to work with less supervision, good work ethics