6 days left
- Full Time
Roles & Responsibilities:
*Review documentation and participate in R&D Phase Reviews
*Aid in coordination of Risk Management activities and file preparation
*Aid in coordination of Post Market Surveillance / Vigilance Reporting
*Communicate specific regulatory requirements to cross functional teams
*Prepare Regulatory Reports for Management as required
Specific Skills Required:
*Qualification: BSc molecular biology or related discipline
*Good Knowledge & understanding of IVD Directive/Regulation or Medical Device Directive/Regulation
*Experience working in ISO 13485 and FDA regulated companies
*Ability to work on own initiative
*Good command of Microsoft Office
*PhD in molecular biology or related discipline
*Experience in preparation of medical device technical files and regulatory submissions
*Good problem-solving skills
Adecco Ireland is acting as an Employment Agency in relation to this vacancy.
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♦ The business of the Adecco Group UK & Ireland is transacted via a number of differently branded trading entities, as follows: Adecco UK Limited, Adia Technology Limited, Modis International Limited, Badenoch and Clark Limited, Ajilon (UK) Limited, Office Angels Limited, Penna plc, Pontoon Europe Limited, Roevin Management Services Limited, Spring Technology Staffing Services Limited.