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GQA Technical and Regulatory Reviewer

Full-time
Posted 3 weeks ago
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Where you can work

Unspecified

Locations named in the listing

  • China
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China - Homebased, China

Remote

Open to candidates in China

View location wording from the posting
China - Homebased, China

Employer description

We exist to create positive change for people and the planet. Join us and make a difference too!

Global Quality & Accreditation (GQA) Technical and Regulatory Reviewer

China- homebased, occasional travel required

About the role

Our Regulatory Services GQA team are looking for a GQA Technical and Regulatory Reviewer who will provide quality management system ownership to medical devices/product certification and QMS audit teams both in China and globally.

Responsibilities

  • Support the roll out of policy decisions and processes for regulatory services and QMS audits in China and globally
  • Provide support of the ISO 13485 certification / product certification and CE schemes, for example investigating customer appeals, report reviewing and supporting activities during regulator audits
  • Deliver certification decisions for ISO 13485 certifications and product certification schemes as eligible, with a goal to being qualified across all non-CE ISO 13485 schemes and product certification schemes, where resource allows
  • Participating in smaller improvement projects ensuring appropriate adherence to procedures
  • Support in hosting regulator or accrediting body audits
  • Provide advice and support to QMS auditors globally, technical specialists, scheme managers, sales, marketing and other BSI colleagues on BSI QMS requirements for medical devices and product certifications.
  • Competence verifier activities to support the auditor qualification process, if appropriate

To be successful in the role, you will have:

  • First or second degree in Engineering, Science, or related discipline
  • A good understanding of QMS requirements as applied in China as well as applicable regulations and standards (ISO 13485, 17021, 17065, MDD, AIMD and/or IVDD, MDR/IVDR and MDSAP requirements in particular)
  • Minimum two years of hands-on manufacturing experience and two years quality management experience; experience of cooordinating or conducting audits of medical device or product certification manufacturers (e.g. supplier or internal audits)
  • Excellent interpersonal and communication skills (written and oral) in Chinese and English

BSI offers a competitive total reward package, an independent and varied job in an international environment, flexible working hours, ongoing training and development with the inclusion of 15-days annual leave, paid sick leave, bank holidays, health insurance, life insurance, maternity leave, nursing leave, paternity leave, paid bereavement leave, learning and development opportunities, and a wide range of flexible benefits that you can tailor to suit your lifestyle.

#LI-remote #LI-LH1

About Us

BSI is a business improvement and standards company and for over a century BSI has been recognized for having a positive impact on organizations and society, building trust and enhancing lives.

Today BSI partners with more than 77,500 clients in 195 countries and engages with a 15,000 strong global community of experts, industry and consumer groups, organizations and governments. Utilizing its extensive expertise in key industry sectors - including automotive, aerospace, built environment, food and retail, and healthcare - BSI delivers on its purpose by helping its clients fulfil theirs. Living by our core values of Client-Centricity, Agility, and Collaboration, BSI provides organizations with the confidence to grow by partnering with them to tackle society’s critical issues – from climate change to building trust in digital transformation and everything in between - to accelerate progress towards a better society and a sustainable world.

BSI is an Equal Opportunity Employer dedicated to fostering a diverse and inclusive workplace.

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Source: Workday