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Gemini Personnel Recruitment Co.,Ltd.Gemini Personnel Recruitment Co.,Ltd.

About Company
Gemini Personnel Recruitment Co., Ltd. is situated in the district of Laem Chabang. The company is licensed by the Ministry of Labour and part of the Gemini group. Gemini Personnel Limited was established in Hong Kong in 1983 and has grown to become Hong Kong’s leading recruitment company with offices in Central and Kowloon. Gemini also has a strong China presence with a joint venture company, J.M. Gemini, in Shanghai, Beijing, Guangzhou and Shenzhen, as well as offices in Singapore and Thailand. We are affiliated internationally through our association with National Personnel Associates of the U.S. We currently source candidates for permanent and temporary roles in a variety of discipline and sectors within the whole Thailand.

For more information please visit us at: http://www.gemini-global.com/
LocationNo.53, Unit 8 1/F, Pier 68, Moo.5, Sukhumvit Road, T. Tungsukla, A. Sriracha District, Chon Buri, 20230, Thailand
Contact personHuman Resources Department
Telephone+66 88-983-8993
Website
  • https://www.gemini-global.com

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: QA&QC Supervisor (Medical Device)

Gemini Personnel Recruitment Co.,Ltd.
Today
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Basic Requirements
Full Time
5 - 7 Year
Central Region
Bachelor's Degree or Higher
30,000 - 40,000 baht/month

Responsibilities
  • Supervise and manage QA/QC operations related to medical device manufacturing to ensure full compliance with applicable quality standards and regulatory requirements.
  • Implement, maintain, and improve Quality Management System (QMS) in accordance with ISO 13485, GMP, and relevant regulatory standards.
  • Lead and supervise QA/QC staff, including task assignment, performance monitoring, coaching, and on-the-job training.
  • Conduct in-process inspections, final product inspections, and quality audits to ensure products meet specifications and customer requirements.
  • Handle non-conformities, root cause analysis, corrective and preventive actions (CAPA), and continuous improvement activities.
  • Prepare and review quality documentation such as SOPs, WI, inspection records, deviation reports, and quality reports.
  • Coordinate with Production, Engineering, and other related departments to resolve quality issues and improve process efficiency.
  • Support internal and external audits (customer audits, ISO audits, regulatory audits) and ensure timely corrective actions.
  • Communicate quality issues and performance reports to management effectively.

Requirements
  • Bachelor’s degree in Engineering, Science, or a related field.
  • At least 5 years of experience in QA/QC within the medical device manufacturing industry.
  • Proven experience in supervising and managing subordinates in a QA/QC or quality-related function.
  • Strong knowledge of ISO 13485, GMP, and medical device quality standards.
  • Experience in quality tools such as CAPA, root cause analysis, and risk management.
  • Ability to communicate in basic to intermediate English, both written and spoken.
  • Strong leadership, problem-solving, and analytical skills.
  • Detail-oriented with a strong sense of responsibility and quality mindset.
  • Able to work effectively in a manufacturing environment and cross-functional teams.

Welfare and Benefits
  • 5-day work week
  • Social security
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