Flexicare Membuka Loker Terbaru Wilayah Serang Banten, Ini Posisi yang Dibutuhkan, Simak Persyaratannya!

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-Coordinate with distributor/ file notification to inform regulatory authorities of Indonesia regarding changes in registered products.

-As and when requested carry out other regulatory/ quality tasks delegated by the manager or senior officers of Flexicare Indonesia.

-Support information request for tender in Indonesia

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Requirement:

-Minimum 1 - 2 years of work experience in Regulatory Affairs for medical device products.

-Possess at least a Bachelor’s Degree in Science from an accredited university.

-Excellent verbal and written communication skills with strong English language proficiency.

-Strong computer skills.

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-Exceptional ability to work independently with minimal supervision, effectively organize, prioritize, and manage multiple projects.

-Positive attitude, strong attention to detail, and ability to solve problems independently.

-Comprehensive understanding of regulatory activities and how they impact other products and/or processes.

-Knowledge of quality management systems, technical file compilation, and Indonesia medical device regulatory requirement