We have a long experience in 3D-printed porous metal and biopolymer scaffolds and we support surgeons in creating tailor-made, tissue-preserving solutions that align with the human body's remarkable self-healing capabilities.We are looking for a new team member willing to participate in the development of the next-generation elastic implants for chest-wall reconstruction and several other cutting-edge projects currently in our pipeline as a Quality and Regulatory Affair (QARA) Manager.Our new team member will support the implementation and documentation of quality and regulatory processes required to obtain market clearance for implantable medical devices, helping to bring innovative technologies to patients.Mandatory requirements:PhD in pharmacy, biomedical or mechanical engineering or related field.Knowledge and/or expertise in quality (ISO 13485) and regulatory (MDR and FDA) processes.Good command of spoken and written Spanish.Good command of spoken and written English.Residence or willingness to relocate to Gran Canaria, Spain.Knowledge of medical device design and manufacturing processes (additive manufacturing, CNC machining) will be highly valued.If this opportunity excites you and you are eager to join a great team on a sunny island while contributing to the development of highly innovative medical devices that improve patients' lives, please do not apply here, but send your CV and a motivation letter (in Spanish or English) to Donato Monopoli (******).Please do not apply if you do not have all the mandatory requirements.
We kindly ask recruitment agencies and headhunters not to submit applications, as they will not be reviewed.
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