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Sr. Regulatory Compliance Engineer 高级合规工程师 16000-20000 收藏 申请职位 主管直聊
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Sr. Regulatory Compliance Engineer 高级合规工程师

16000-20000
广东-东莞 -东坑镇 | 5年以上经验 | 本科学历
2026-06-12 更新 被浏览:
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职位描述
到岗时间:不限 婚况要求:不限 职位概要(Job summary): The Regulatory Compliance Sr. Engineer is to monitor and ensure the compliance to external standards/requirements and Quasar Quality System Requirements in Quasar manufacturing site. 工作职责(Responsibilities): 1. Conduct routine monitoring, checking program to identify site compliance gaps and follow up gap remediation. 2. Participate in Corporate Procedure Development & Maintenance. Join Corporate audit On other sites when required. 3. Provide Regulation Compliance supporting On critical business projects, when necessary, e.g., MAH 4. Facilitate critical external audits/inspection at site. e.g., FDA inspection, NMPA audits. 5. Join cross sites QMS IT system coordination and maintenance. 6. Responsible for liaising with the company’s internal/external stakeholders to identify/understand the required Regulatory Compliance knowledge needed to provide the required expertise and advice. 7. Other tasks assigned by leader. 任职资格(Qualification) : 1. Bachelor or Master’s degree in science related field. 2. Minimum of 5 years’ experiences On Medical Device or Pharmaceutical Industry Quality Regulatory Compliance related work. Knowledgeable On international standards or Health Authorities regulations requirement. 3. Good oral and written communication skills both in English and Chinese. 4. Good interpersonal and influential skills. 5. Ability to work under pressure in a dynamic environment.
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会员等级
  • 200-500人
  • 500万
职位概要(Job summary): The Regulatory Compliance Sr. Engineer is to monitor and ensure the compliance to external standards/requirements and Quasar Quality System Requirements in Quasar manufacturing site. 工作职责(Responsibilities): 1. Conduct routine monitoring, checking program to identify site compliance gaps and follow up gap remediation. 2. Participate in Corporate Procedure Development & Maintenance. Join Corporate audit On other sites when required. 3. Provide Regulation Compliance supporting On critical business projects, when necessary, e.g., MAH 4. Facilitate critical external audits/inspection at site. e.g., FDA inspection, NMPA audits. 5. Join cross sites QMS IT system coordination and maintenance. 6. Responsible for liaising with the company’s internal/external stakeholders to identify/understand the required Regulatory Compliance knowledge needed to provide the required expertise and advice. 7. Other tasks assigned by leader. 任职资格(Qualification) : 1. Bachelor or Master’s degree in science related field. 2. Minimum of 5 years’ experiences On Medical Device or Pharmaceutical Industry Quality Regulatory Compliance related work. Knowledgeable On international standards or Health Authorities regulations requirement. 3. Good oral and written communication skills both in English and Chinese. 4. Good interpersonal and influential skills. 5. Ability to work under pressure in a dynamic environment.
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