Job Description

  1. Control, prepare and edit registration documents for ISO9001 / ISO17025 / ISO13485, GMP
  2. Manage, control, store, distribute, recall, and make a request for approval of internal and external document destruction
  3. Make classification and control document listing accounts
  4. Coordinate all departments to comply work quality in accordance with ISO9001 / ISO17025 / ISO13485, GMP
  5. Control all documents from the head office and document control centers from each department
  6. Carry out planning for internal & external audit
  7. Track the results of the entire CAR / PAR solution
  8. Administer the document processing request
  9. Do some other assignments from executives / QMR

Qualifications

  1. Bachelor’s degree in related field
  2. Male / Female age between 25-45 years
  3. Having experience in ISO and GMP documents for at least 2-5 years
  4. Having knowledge in ISO 9001/13485/17025 and GMP will be an advantage
  5. Be able to solve immediate problems and carry out work plan efficiently
  6. Having good human relations, good coordinative skills, and teamwork spirit
  7. Having leadership skill and be able to complete documentation and training
  8. Having good computer skills (Word, Excel, Powerpoint)
  9. Be able to start working immediately
Welfare

  • Social Security
  • Uniform
  • Annual party
  • Annual health checkup
  • Overtime pay (some positions)
  • Funeral allowance (staff, parents and children)
  • Others as required by law
Application Method    – Apply via email

Contact

Ms. Thitaree
Aeonmed Company Limited
72/1 Village No. 5, Khlong Mai Subdistrict, Sam Phran District, Nakhon Pathom Province 73110
Phone : 034-326-925 to 7 ext. 211
Email : hr@aeonmed.co.th (for contact and job application).
Website : www.aeonmed.co.th
Work LocationKhlong Mai Subdistrict, Sam Phran District, Nakhon Pathom Province