A global certification service leader that is recognised as the benchmark within quality and integrity are looking for multiple Technical File Reviewers for Non-Active Devices. As an accredited Certified Body and MDR approved Notified Body they provide global market access by testing and certifying products/ systems for international quality and safety standards.
Role:
- Responsible for planning and executive audits in accordance to ISO 13485, MDD, MDR and MDSAP
- Conduct Technical File reviews of specific authorized products
- Direct assessments in accordance with recognised procedures
- Deliver assessment and certification services to meet customer requirements and appropriate accreditation standards
- Manage auditing teams to maximise efficiency and to enhance client satisfaction whilst ensuring compliance with standards
Requirements:
- Bachelor's degree in technical field -
- Minimum 4 years' work experience within medical device industry - 2 years' in design, manufacturing, testing or Audit/ Assess
- Fluent English
