• Review audit packs to verify data and their content for compliance with MDD 93/42 EC or MDR (EU) 2017/745 • Verify that audit documentation for QMS on-site as well as technical documentation assessment complies with medical device regulations • Ensure that major non-conformity and any unsolved issues are addressed before transferring the audit pack for certification decision • Review whether the final review has been carried out by an approved Final Reviewer • Make the final decision as to whether a certificate should be issued • Check audit packs for QMS on-site audit for MDD / MDR / ISO13485 • Contribute to meeting operations objectives and Key Performance Indicators to deliver certificates to customers

• Review audit packs to verify data and their content for compliance with MDD 93/42 EC or MDR (EU) 2017/745 • Take decision on reviewed audit packs to determine if the certificate shall be issued • Verify that audit documentation for QMS on-site is in compliance with the medical device regulations • Review whether the final review has been carried out by an approved Final Reviewer • Ensure full compliance with the Company’s Code of Integrity & Professional Conduct • Report data on your daily workload and any technical issue.

• Review audit packs to verify data and their content for compliance with MDD 93/42 EC or MDR (EU) 2017/745 • Determine if the certificate shall be issued and if there is any applicable restrictions • Verify that audit documentation for QMS on-site and technical documentation assessment is in compliance with medical device regulations • Verify that all major non-conformity and any unsolved issue has been addressed and closed out • Review whether the final review has been carried out by an approved Final Reviewer • Ensure full compliance with the Company’s Code of Integrity & Professional Conduct • Reporting data on your daily workload and any technical issue

• Review audit packs to verify data and compliance with MDD 93/42 EC or MDR (EU) 2017/745 • Make decisions on reviewed audit packs to determine certificate issuance • Verify compliance with medical device regulations and internal procedures • Check audit packs for QMS on-site audit for MDD / MDR / ISO13485 • Collaborate with auditors and medical device certification teams