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03 September 2019
Job ID: JKT-32439
REGULATORY AFFAIRS

Responsibility :

  • To acquire the medical device registration approval from Indonesian MOH (Ministry of Health)
  • To prepare and submit registration documents for company products that are requested to be sold in the Indonesian local market
  • To carry out the process of registering Medical Device products
  • To request the application of the Free Sales Certificate to BPOM / Ministry of Health and the legalization process from the embassy of the relevant ministries

Qualification :

  • Pharmacist graduates preferred (Fresh Graduates are preferred), GPA min. 2.50
  • Regardless of Age
  • Having knowledge on medical devices
  • Knowing licensing about OSSs, pharmaceutical licensing, drug registration and medical devices
  • Understanding CPOB is preferred
  • Fluent in English both writing and speaking (submitting official TOEFL score will be advantaged)
  • Possible to use office software (Microsoft Office Word, Excel, Power Point, etc.)
  • Good communication skills
  • Complying with company policies
  • Good attitude and personality
  • Good analytical skills and thorough / attention to details.
  • Fast learners, hardworking, disciplined, creative and proactive. Can work in teams or work independently. Able to deal with tight deadline pressures.

Please send your application + photograph by clicking

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Job Details:
  • Employment Type:
    Full Time
  • Career Level:
    Entry Level
  • Company Industry:
    Legal Services
  • Location:
    South Jakarta, Jakarta, Indonesia
  • Salary:
    Salary negotiable

Benefits:
  • Five-day work week

ICT WORLDWIDE INDONESIA, PT
Dentium Co., Ltd. was founded in South Korea in June 2000 as the first company to successfully achieve the S.L.A. (Sandblasting with Large grits and Acid etching) surface treatment technology. Ever since its establishment, Dentium has collaborated with leading clinicians, research institutes, and universities to develop and offer the state-of-the-art products to make dental implant surgeries easier and more predictable. To ensure that Dentium offers products highest in quality, Dentium attained the ISO13485 and CE (Europe) certification and met the good manufacturing standards (GMP) from many countries worldwide, including the United States Food and Drug Administration (FDA). Dentium is globally recognized as a company dedicated to research and development. Dentium began with the manufacturing of high quality dental implant products and related instruments. Over time, to complement its dental implant systems, Dentium has embarked in developing regenerative materials. Moreover, Dentium has expanded its presences in the field of dentistry by developing and manufacturing lab products (Zirconia Blocks, Porcelain) and equipment for Digital Dentistry (CAD/CAM System, iOS). In addition to the R&D, Dentium is highly regarded for its commitment to providing edifying scientific programs. Every year, Dentium organizes Dentium World Symposium, Clinical Case Presentations, and seminars, where thousands of dental professionals from all around the world attend to share their professional experiences and knowledge in the field of dental implant, restorative, and digital dentistry. Dentium will continue to meet the demands of our valued customers by providing the highest of quality products, comprehensive educational programs, and unrivalled customer service to dental professionals worldwide. It is an honor to have you as our valued customer.
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