Deskripsi Pekerjaan

COMPANY CATEGORY : 

Japanese Medical Equipment Manufacturing

JOB SUMMARY : 

  • Compilation data related Quality
  • Coordinate for regulatory/registration process (all domestic and overseas)
  • Manage and direct a team of skilled, semi skilled and technically individuals
  • To manage Regulatory Affair, QMS ISO 13485, Risk Management Plan/RMP, Clinical Evaluation, REACH, Verification & Validation, Calibration, Audit (Regulatory, Customer, Supplier, and Internal),
  • Corrective and Preventive Action/CAPA, Complaint Handling, Product Release, Device History Record/ DHR, Change Control, Monthly meeting, Management review meeting, Design History File/DHF

EXPERIENCE, REQUIREMENTS & SKILLS : 

  • Education: Bachelor Degree Chemical/Pharmacy/Biology major
  • Language: English Intermediate Level
  • Experience: 5 years in medical device/ Pharmaceutical/FMCG manufacturing
  • Experience in concept of CPAKB, GMP
  • Must have capabilities: Leadership, Project Management, Performance Evaluation, Analytical thinking, Independent, Judgment.
  • Preferably Assistant manager/senior supervisor specialized in manufacturing Quality Assurance/Control or equivalent

BENEFIT:

  • THR
  • BPJS
  • Meal
  • Transportation
  • Detail will be discussed in the interview

 

ONLY CV IN ENGLISH WILL BE PROCESSED

Tentang Perusahaan

No. Telepon

0215705290

Address

Prince Center , Floor 4 , Jl. Jend. Sudirman Kav 3-4 Jakarta Pusat 10220, Indonesia