Associate Ii, Complaints (korean Speaker)

467

Seoul, South Korea
Not specified; not specified; comprehensive benefi...
Fluent in written and spoken korean
Medical device vigilance regulations
Adverse event complaint handling
The role is responsible for the day-to-day submission of regulatory reports to local health authorities for medical devices in Korea

Job Summary

  • The role is responsible for the day-to-day submission of regulatory reports to local health authorities for medical devices in Korea.
  • Candidates must manage technical and adverse event complaint records while ensuring compliance with local and international regulations.
  • Alcon offers a competitive compensation package, comprehensive benefits, and opportunities for continuous learning within a diverse team.

Matching Summary

The role is responsible for the day-to-day submission of regulatory reports to local health authorities for medical devices in Korea.

Salary

Not specified; Not specified; Comprehensive benefits included

Skills & Requirements

Must-have

  • Fluent in written and spoken Korean
  • Medical device vigilance regulations
  • Adverse event complaint handling
  • Regulatory report submission
  • Quality system documentation

Nice-to-have

  • Mandarin language skills
  • Experience with multinational pharma companies
  • Optometry or pharmacy degree background
  • Continuous improvement mindset
  • Audit support experience

Key Requirements

  • 1-2 years experience in pharmaceutical or medical device industries
  • University degree in Science or healthcare discipline
  • Fluency in English and Korean languages

Work Rights

Not specified

Tailored Resume

Cover Letter