Job Description
Regulatory Compliance Assistant
Job type: ContractSalary: NegotiableLocation: HesseReference: RE-32544162
For one of the largest medical retailers in Germany, we are looking for a "Regulatory Compliance Assistant" in Hesse from now on.
Responsibility and responsibility:
* Ensuring the completeness and up-to-date technical documentation of all Private Label products in accordance with the EU Medical Product Directives (MDD and IVD)
* Maintaining the global database with regard to the correctness of the medical product classes, CE certification, sales restrictions and country of origin. This care refers to all the worldwide available private label articles
* Creation of required declarations of conformity and other documents by the regulatory side for the distribution of own label products in the local organizations Are required.
* Communication with notified bodies (Notified Bodies)
* Procurement of necessary documents, such as sterile certificates, product analyzes and declarations of conformity with the manufacturers of own-
label products Technical requirements:
* Very good knowledge of English
* Experience in medical technology - ISO 13485
* Experience in In vitro diagnostics
framework data:
* project duration: 6 months
* workload: 40h / w full-time
* region: Hessen
If interested, I look forward to your feedback with your current resume under a.wiegand (at) realstaffing.com or call +49 69 264 89
8050. For more information on Real Staffing, please visit www.realstaffing.com/Com / deCom / deSterile certificates, product analyzes and statements of compliance with the manufacturers of private label products Professional Requirements: * Fluency in English * Experience in medical technology - ISO 13485 * Experience in the In Vitro Diagnostics Framework data: * Project Duration: 6 months * Workload: 40h / w full-time * Region: Hessen If you are interested, I would be pleased to receive your feedback with your current CV under a.wiegand (at) realstaffing.com or by telephone at +49 69 264 89 8050. For more information on Real Staffing, please visit www.realstaffing.com/Sterile certificates, product analyzes and statements of compliance with the manufacturers of private label products Professional Requirements: * Fluency in English * Experience in medical technology - ISO 13485 * Experience in the In Vitro Diagnostics Framework data: * Project Duration: 6 months * Workload: 40h / w full-time * Region: Hessen If you are interested, I would be pleased to receive your feedback with your current CV under a.wiegand (at) realstaffing.com or by phone at +49 69 264 89 8050. For more information on Real Staffing, please visit www.realstaffing.com* Very good knowledge of English * Experience in medical technology - ISO 13485 * Experience in In Vitro Diagnostics Cream data: * Project duration: 6 months * Utilization: 40h / w Vollzeit * Region: Hessen I am looking forward to your feedback with your current CV Under a.wiegand (at) realstaffing.com or call +49 69 264 89 8050. For more information on Real Staffing, please visit www.realstaffing.com/en* Very good knowledge of English * Experience in medical technology - ISO 13485 * Experience in In Vitro Diagnostics Cream data: * Project duration: 6 months * Utilization: 40h / w Vollzeit * Region: Hessen I am looking forward to your feedback with your current CV Under a.wiegand (at) realstaffing.com or call +49 69 264 89 8050. For more information on Real Staffing, please visit www.realstaffing.com/enHessen If you are interested, I would be pleased to receive your feedback with your current CV under a.wiegand (at) realstaffing.com or by phone at +49 69 264 89 8050. For more information on Real Staffing, please visit www.realstaffing.comHessen If you are interested, I would be pleased to receive your feedback with your current CV