Latest Vacancies

We currently have several vacancies for Medical Device Design Engineers, Quality Engineers, Regulatory Specialists, and Business Development Associates, in Sushvin Consultancy Services.

Please apply in writing with a cover letter and CV to: info@sushvin.com

Services We Offer.

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Medical Device Regulation 2017/745

Medical Device Quality Assurance & Compliance, ISO13485: 2016 Quality Management Services, Medical Device Regulation 2017/745 QMS Transition

Quality Assurance & Compliance

Auditing Solutions, Intenal Audit

Auditing Solutions

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Brexit Transition

PRRC - Person Responsible For Regulatory Compliance, Medical Device Registrations, UK Registration, Global Registration, MDSAP (Medical Device Single Audit Program)

PRRC - Person Responsible For Regulatory Compliance

UK Responsible Person, UKRP, legal medical device/IVD, UK MDR 2002

UK Responsible Person

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Medical Device Registrations

PMS - Post Market Surveillance/PMCF,

PMS - Post Market Surveillance/PMCF

Clinical Evaluation Reports (CER)

Clinical Evaluation Reports

Software As A Medical Device, MDR 2017/745 and IVDR 2017/746

Software As A Medical Device

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Combination Drug Device Support

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