医疗器械管理体系审核员 - Shanghai

+This position involves conducting audits on medical devices in accordance with ISO 13485 standards.We are looking for an experienced auditor who can work independently and face challenges. · ...

This is an audit manager position for medical devices with requirements such as ISO 13485 standard and EU regulations. · Responsibilities include conducting audits efficiently, writing reports and performing compliance reviews. · Bachelor's degree or above in biomedical engineeri ...

We are seeking passionate individuals like you to join our dynamic team.This position is responsible for conducting audit/technical documentation review according to standard requirements regulatory requirements procedures and code of conduct. · ...

Conduct audit tasks efficiently in accordance with the ISO 13485 and EU regulations. · Write audit reports according to the requirements. · Issue deficiency reports for findings during the audit. · ...

We are seeking passionate individuals to join our dynamic team. · This position conducts audit/technical documentation review in Non-Active Medical Product of Central region, · responsible for customer communication and supporting relevant in NAM field for customer service and co ...

We are seeking passionate individuals like you to join our dynamic team.This position is responsible for conducting audit/technical documentation review in Non-Active Medical Product (NAM) of Central region. · ...

This role involves conducting audit/technical documentation review for Active Medical Product (AMP) / Non-Active Medical Product (NAM) products in order to satisfy international market access requirements. · ...

We are looking for a Product Certification Auditor to play a key role in maintaining product excellence. In this role you'll conduct product certification assessments across diverse environments ensuring compliance with BSI's rigorous certification schemes and Kitemark standards. ...

We are recruiting for an auditor to support our product certification business in delivering assessments against either construction products (CPR), gas appliances (GAR or PED) or BIM( Building Information Modelling /PAS 19650. · The ideal candidate will have expertise in sustain ...

We are proud to be the business improvement company for other organisations to become more sustainable and resilient and finally to inspire trust in their products, systems, services, and the world we live in. · ...

该职位负责规划、推动专业管理体系审核、评估和认证服务以及提供技术支持。 · 大学本科及以上学历,医疗器械或相关学科如:医学、药理学、生物医学工程、微生物学、生物技术、生物化学; · 具有4年及以上从事与医疗器械相关领域的工作经验(包括开发,测试,设计,质量监控等); · ...

执行医疗器械质量体系认证服务,如MDSAP, ISO13485, MDR/IVDR QMS等; · 协助推动医疗器械质量体系业务发展,为客户提供有价值的技术支持; · 根据客户需求策划和提供专业培训等。 · ...

+The position involves updating and maintaining the company's quality management system to ensure compliance with ISO 9001 standards. · +Participate in internal audits of the organization's quality system. · External audits preparation, including customer audits. · ...

This position is for a medical device consultant with experience in quality system related fields such as GMP/ISO13485/QSR820. The ideal candidate should have fluent English reading and writing skills, with oral fluency being preferred. · ...

As QA Manager responsible for managing relabeling activities in 3rd party warehouses. · Establish and maintain quality specifications and control plans for relabeled products · Perform process validation for relabeling · ...

As QA Manager responsible for managing relabeling activities in 3rd party warehouses establishing and maintaining product quality control procedures based on the company's Quality Management System for Medical Device Commercial operations to ensure supplied medical devices meet a ...

As QA Manager responsible for managing relabeling activities in 3rd party warehouses establishing and maintaining product quality control procedures based on the company Quality Management System for Medical Device Commercial operations to ensure supplied medical devices meet req ...

This position is responsible for maintaining SMCN's Quality Management System by ensuring company procedures comply with regulatory and ISO requirements. · Bachelor's degree in engineering and/or manufacturing related fields preferredMust have 2+ years of quality management exper ...

This job is with Johnson & Johnson an inclusive employer. · Assist in production process risk management and process control. · As production process risk management and process control coordinator assist in maintaining risk management documents on-site IPQA material disposition ...

At Johnson & Johnson, we believe health is everything. · ...