投诉处理质量工程师
常州市康辉医疗器械有限公司
- 公司规模:500-1000人
- 公司性质:外资(欧美)
- 公司行业:医疗设备/器械
职位信息
- 发布日期:2016-12-15
- 工作地点:常州
- 招聘人数:1人
- 工作经验:3-4年经验
- 学历要求:本科
- 职位月薪:1-2/月
- 职位类别:质量管理/测试工程师(QA/QC工程师) 售前/售后技术支持工程师
职位描述
职位描述:
工作经验及相关技能要求/Working experience and relative skill requirements:
1. Education / Degree Required: Junior college or above in Medical/Clinical Field, Science, Pharmacy, Biomedical Engineering Background
2. Job Experience: 3 year+ , experience in a foreign medical device or pharmaceutical industry company is preferred, especially in customer complaint.
3. Bilingual: English/Mandarin required.
4. Team interpersonal: partnering, interaction, feedback, negotiating, training.
5. Strong communication, problems solving and continuous improvement.
6. Customer focus, accountable and responsive
7. Knowledge of related regulatory policy ISO13485 and ADR requirements is preferred
职位职责/Responsibility:
1. Collect and handle customer compliant that cover all product units in the Kanghui Medical.
2. Run and maintain the complaint handling system and consistently generate and preserve data and report as required.
3. Report suspicious ADR (Adverse Device Report) to related functional team for further evaluation.
4. Communicate and coordinate with related functional department to address critical complaint case.
5. Improve compliant handling process to enhance process effectiveness & efficiency and compliance to corporate requirements.
6. Maintain compliant files to ensure the ISO, QSR, MDD, GMP & corporate requirements are met.
7. Collect returned devices and send to each product's VSM for analysis, deliver the replacement to customer.
8. Other assignment by QA manager.
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工作经验及相关技能要求/Working experience and relative skill requirements:
1. Education / Degree Required: Junior college or above in Medical/Clinical Field, Science, Pharmacy, Biomedical Engineering Background
2. Job Experience: 3 year+ , experience in a foreign medical device or pharmaceutical industry company is preferred, especially in customer complaint.
3. Bilingual: English/Mandarin required.
4. Team interpersonal: partnering, interaction, feedback, negotiating, training.
5. Strong communication, problems solving and continuous improvement.
6. Customer focus, accountable and responsive
7. Knowledge of related regulatory policy ISO13485 and ADR requirements is preferred
职位职责/Responsibility:
1. Collect and handle customer compliant that cover all product units in the Kanghui Medical.
2. Run and maintain the complaint handling system and consistently generate and preserve data and report as required.
3. Report suspicious ADR (Adverse Device Report) to related functional team for further evaluation.
4. Communicate and coordinate with related functional department to address critical complaint case.
5. Improve compliant handling process to enhance process effectiveness & efficiency and compliance to corporate requirements.
6. Maintain compliant files to ensure the ISO, QSR, MDD, GMP & corporate requirements are met.
7. Collect returned devices and send to each product's VSM for analysis, deliver the replacement to customer.
8. Other assignment by QA manager.
职能类别: 质量管理/测试工程师(QA/QC工程师) 售前/售后技术支持工程师
公司介绍
美敦力是全球领先的医疗科技公司,成立于1949年,总部位于美国明尼苏达州的明尼阿波利斯市。1957年美敦力发明了全球***台由电池驱动的便携式体外心脏起搏器,奠定了美敦力以医疗科技帮助全球患者“减轻病痛、恢复健康、延长寿命”的企业使命和领导地位。每一秒钟,全球就有超过2 位患者受益于美敦力的医疗技术或疗法。
康辉医疗隶属于美敦力恢复性疗法业务集团,同时也是我国骨科行业的领先企业、国家重点高新技术企业、全国外科植入物和矫形器械标准化技术委员会委员单位,一直专注于脊柱、创伤和关节置换等植入物及其手术器械的创新探索,其产品的多元化组合更是广泛应用于人体创伤修复、脊柱矫形等骨科疾病治疗领域。
公司重视每位员工的独特价值,鼓励员工以与众不同的思维模式,解决问题,不断进取,锐意创新,我们特别注重员工的专业技能和领导才华,为其提供丰富的学习机会及多样化职业发展路径。欢迎您加入我们,成为我们的一员。
康辉医疗隶属于美敦力恢复性疗法业务集团,同时也是我国骨科行业的领先企业、国家重点高新技术企业、全国外科植入物和矫形器械标准化技术委员会委员单位,一直专注于脊柱、创伤和关节置换等植入物及其手术器械的创新探索,其产品的多元化组合更是广泛应用于人体创伤修复、脊柱矫形等骨科疾病治疗领域。
公司重视每位员工的独特价值,鼓励员工以与众不同的思维模式,解决问题,不断进取,锐意创新,我们特别注重员工的专业技能和领导才华,为其提供丰富的学习机会及多样化职业发展路径。欢迎您加入我们,成为我们的一员。
联系方式
- Email:h.k@kanghui-med.com
- 公司地址:地址:span江苏省常州市新北区长江北路西江路11号