– Recording and monitoring of complaints status,
– Assess the complaints acc. to Cefra N°10246*05,
– Caring out all correspondence with ANSM in regards of vigilance,
– Caring out all correspondence with MD manufacturers in regards of complaints/vigilance/FSCA related with it devices,
– Assisting in recall process, strict cooperation with MD manufacturers and ANSM in recall process,
– Responsibility for proper identification, traceability and records (including archiving) generated during complaint and vigilance process.
Please add both of the following clauses:
I consent to the processing of my personal data for the purposes of the recruitment process carried out by Lina Medical Polska Sp. z o.o. (in accordance with the Act of May 10, 2018 on the protection of personal data (Journal of Laws of 2018, item 1000) and in accordance with the Regulation of the European Parliament and of the Council (EU) 2016/679 of April 27, 2016 on the protection of persons natural persons in connection with the processing of personal data and on the free movement of such data and the repeal of Directive 95/46 / EC (GDPR)).
I also consent to the processing of my personal data for the purpose of future recruitment by the above-mentioned company.
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