HRchannels Group - Headhunter Vietnam

Vice Quality Manager (Medical devices/Pharma)

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Job Detail

  • Offerd Salary (USD) $1700
  • Career Level Trưởng Nhóm/ Giám sát
  • Experience 3-5 Years
  • Gender Male/Female
  • Sector Hà nội, Hải Phòng, Hải Dương
  • Industry Chăm sóc sức khỏe/Thiết bị Y tế, Dược/Công nghệ sinh học, QA/QC

Job Description

Dream Job Alert! Become a Vice Quality Manager (Medical devices/Pharma, ID19669) at a foreign-invested company and earn $1700/month:
  • Assist in establishing, implementing, and maintaining the Quality Management System (QMS) in compliance with GMP and applicable ISO standards (ISO 13485 / ISO 13484).
  • Ensure all manufacturing and production activities comply with regulatory requirements and internal quality standards for medical devices.
  • Participate in the preparation, implementation, review, and continuous improvement of SOPs, quality manuals, and related quality documentation.
  • Manage and oversee ISO Class 8 cleanroom operations in accordance with GMP and regulatory requirements.
  • Ensure strict adherence to cleanroom standards, including environmental monitoring, hygiene practices, and contamination control.
  • Supervise validation, qualification, and routine monitoring of cleanroom facilities, systems, and equipment.
  • Support and participate in internal audits, external audits, and inspections conducted by regulatory authorities and certification bodies.
  • Prepare audit documentation and reports, manage corrective and preventive actions (CAPA), and ensure timely closure of identified non-conformities.
  • Deliver GMP, ISO, and cleanroom compliance training to production and quality personnel.
  • Support the Quality Manager in supervising quality staff and coordinating quality-related activities across departments.

Requirement

  • Male or female, under 45 years old.
  • University degree in Pharmacy (licensed pharmacists are preferred).
  • 3–5 years of experience in the position of Quality Manager or Deputy Manager in the medical device or pharmaceutical manufacturing industry.
  • Proficient in English.
  • Direct experience working with customers and managing cleanroom operations in compliance with GMP quality standards; ISO Class 8 cleanroom experience is highly preferred.

Required skills

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