دعوت به همکاری مجموعه Rico Solutions
مجموعه Rico Solutions برای تکمیل کادر خود در تهران به افراد واجد شرایط زیر نیازمند است:
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The Opportunity
Work within a growing, well-established Medical Device consultancy and compliance company.
Providing medical device products supporting development and Quality standards.
What is needed for me to be considered?
Experience of both ISO 13485, FDA 21 CFR 820 & European medical device requirements (MDD 93/42/EEC, and MDR (EU) 2017/745) is mandatory.
Experience in implementation of quality management systems (QMS) and Risk Assessment Documentation.
Experience in creation of technical files to both MDR 2017/745 and IVDR 2017/746
Experience in product registrations in EU, USA and rest of the world.
At least 3 years’ experience working in a regulated medical device manufacturing environment.
English language skills are mandatory
Computer skills required (Word, Excel, and Power Point etc.).
Good organisational skills and the ability to work to deadlines.
Good communication skills are essential
Flexibility and the ability to re-prioritise workload are essential due to changing priorities of the team.
The job holder must be a team player and be able to handle work of a confidential nature.
Educated to Degree level, preferably in Life Sciences
A willingness to develop knowledge or experience of medical device compliance field.
Willing to travel, as required
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Quality and Regulatory Affairs (QRA) Specialist in Medical Devices
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متقاضیان واجد شرایط می توانند از طریق راه های ارتباطی اعلام شده در آگهی درخواست خود را جهت استخدام ثبت نمایند.
