Career Development Hub

Hello Exemplar Community,

Over the last year, I worked hard to obtain my certification in ISO13485 and MDSAP through Exemplar Global.  With over 20 years of benchtop experience in Research and Development and IVD and medical device development and manufacturing, I can provide a thorough perspective of any medical device manufacturer's  QMS.  I am looking for more opportunities to use my newly acquired Medical Device Quality Auditing skills to help companies with Internal Audit needs, determine audit readiness and help prepare them for certification. 

If anyone has any suggestions or leads on how to gain more auditing experience, please reach out.

Regards,

Nanda Filkin

nanda.filkin@aretebiosciences.com

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Nanda Filkin
QA Scientist
Arete Biosciences
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Congratulations on achieving your ISO 13485 and MDSAP certifications. Combining auditing credentials with more than 20 years of hands-on R&D and medical device manufacturing experience creates a very strong profile, especially in the IVD sector. Many organizations value auditors who understand both compliance requirements and real operational challenges. Internal audits, supplier audits, and mock inspections are excellent ways to continue building audit experience and industry visibility. Wishing you success as you expand into this next stage of your career.

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Francisco J. Tapia Guerrero
ftapia@qualitascertification.com
www.linkedin.com/in/franktapiaguerrero
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Good afternoon

Well done

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Shikwambane
Pretoria
South Africa
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Original Message:
Sent: 05-18-2026 04:36 AM
From: Francisco J. Tapia Guerrero
Subject: ISO13485 and MDSAP Auditing Opportunities

Congratulations on achieving your ISO 13485 and MDSAP certifications. Combining auditing credentials with more than 20 years of hands-on R&D and medical device manufacturing experience creates a very strong profile, especially in the IVD sector. Many organizations value auditors who understand both compliance requirements and real operational challenges. Internal audits, supplier audits, and mock inspections are excellent ways to continue building audit experience and industry visibility. Wishing you success as you expand into this next stage of your career.

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Francisco J. Tapia Guerrero
ftapia@qualitascertification.com
www.linkedin.com/in/franktapiaguerrero
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Hi Nanda,

Congratulations on the credentials and vast experience in the medical device world. I sent you a direct message. We have a need in the 13485 and QSR domain that might be of interest. My direct email is james@concentricglobal.co and LinkedIn at https://www.linkedin.com/in/jimthompson2001/.

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All the best,
James

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James R. Thompson
COO/CIO & Technical Leader
Concentric Global | Office: 843.608.0127
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