Regulatory Affairs Lead – Product Registration & Labeling

The Estée Lauder Companies Inc.; Jakarta Pusat; On-site; IDR 180,000,000 - 320,000,000; Full time

Job summary

The Estée Lauder Companies Inc. is seeking a Regulatory Affairs professional to manage local product registration requests in Indonesia and to oversee end-to-end registration processes, including PIF preparation and filing to BPOM and the Ministry of Health.

You will proactively identify challenges with the OSS BKPM system and ensure labeling and claims meet local regulatory requirements. Responsibilities include coordinating with Global Regulatory Affairs, Brand, and Supply Chain teams to meet

Qualifications

• Experience in retailing corporations or FMCG is preferable.
• Diplomacy with strong listening and analytical skills.
• Good oral and written communication skills.
• Willingness and openness to change processes.

Responsibilities

• Liaise with Global Regulatory Affairs to obtain the needful documents / requirements to ensure timely submission and approval of products registration with Indonesia authority, e.g. BPOM and Ministry of Health.
• Liaise with Affiliate Demand Planner and Brand team to track all product registration request and schedule submission accordingly to meet NPL timing.
• Track and manage all product registration approval, prepare renewal of product registration schedule to ensure validity continuity for all in-market products.
• Proactive external engagement to create and sustain competitive advantage.
• Connect with Supply Chain to ensure product label comply with local regulation.
• Connect with Brand team to ensure product claim comply with local regulation.
• Report and monitor progress of all issues arises from product registration process, escape for timely resolution.

Job description

The Estée Lauder Companies Inc. is seeking a Regulatory Affairs professional to manage local product registration requests in Indonesia and to oversee end-to-end registration processes, including PIF preparation and filing to BPOM and the Ministry of Health.

You will proactively identify challenges with the OSS BKPM system and ensure labeling and claims meet local regulatory requirements. Responsibilities include coordinating with Global Regulatory Affairs, Brand, and Supply Chain teams to meet