Global Regulatory Affairs Specialist — Training & Growth

PT. Daewoong Group Indonesia; Jakarta Utara; On-site; IDR 200,880,000 - 357,120,000; Full time

Job summary

Daewoong Indonesia is seeking a Regulatory Affairs professional to coordinate registrations for drug, cosmetics, and medical devices, ensuring GMP compliance and regulatory alignment across regional and global stakeholders.

The role requires a life-sciences degree and strong English; you will learn from Korea HQ with structured training and growth programs, supporting a central RA team in a dynamic, internationally connected environment.

Qualifications

• Bachelor’s degree in Pharmacy or life sciences required.
• Excellent written and verbal English communication.
• Knowledge of medicines, cosmetics, and medical devices regulations.
• Experience in regulatory affairs is preferred.

Responsibilities

• Coordinate, compile and submit technical registrations for drug/cosmetics/medical devices to regulatory authorities.
• Ensure compliance with local and international regulations and interpretations.
• Monitor regulatory changes and registration status for local, regional, and global stakeholders.
• Support RA team with reporting, strategy guidance, and meeting preparation.

Skills

Regulatory knowledge

English proficiency

Interpersonal skills

Self-learning

Education

Bachelor's degree in Pharmacy / Chemistry / Biology or life sciences

Job description

Daewoong Indonesia is seeking a Regulatory Affairs professional to coordinate registrations for drug, cosmetics, and medical devices, ensuring GMP compliance and regulatory alignment across regional and global stakeholders.

The role requires a life-sciences degree and strong English; you will learn from Korea HQ with structured training and growth programs, supporting a central RA team in a dynamic, internationally connected environment.