PpTo reinforce our Regulatory Affairs and Quality Assurance department, and to continue our business expansion with new market introduction, especially the USA, we are looking to fill the position of: /p h3bSenior Regulatory Affairs Design Quality Engineer /b /h3 pReporting to the Regulatory Affairs Manager, you are responsible for the following activities, in accordance with applicable regulatory requirements (EU, US, AU, UK, CH, etc) and leveraging your background and demonstrated experience in medical device manufacturing: /p ul libRegulatory Interactions: /b You are the primary point of contact for interactions with Competent Authorities (ANSM, FDA, TGA, MHRA, Swissmedic, …) and our European Notified Body. You prepare, argue, and defend Symbios technical and regulatory positions in the context of pre- and post-market submissions (Tech. Doc., 510k, changes notification), audits, inspections, and other queries, demonstrating the ability to engage constructively and effectively with external regulatory stakeholders whilst maintaining the necessary sense of urgency. /li libDesign and Development /b: You support Engineering teams in the design and development of medical devices to demonstrate compliance with regulatory requirements, applicable standards and other relevant regulations. You support risk management activities as appropriate. Thanks to your engineering and analytical skills, you review and approve quality records to ensure they meet established regulatory and quality requirements. You compile and maintain Tech. Doc. and 510(k) as appropriate. /li libCompliance /b: You provide the necessary support to ensure that QMS processes under the responsibility of the regulatory team are applied (Change Control, Risk Management, CAPA, …). You act as process owner for those within your scope, guaranteeing their compliance, control, and continuous improvement. You are also responsible for ensuring that Symbios’ obligations regarding the importation and distribution of non-Symbios products are appropriately fulfilled. /li libRegulatory Intelligence /b: You interpret and apply medical devices regulations, including FDA QMSR and the EU MDR, and play an instrumental and active role in their deployment within the organization. /li libCross-functional collaboration /b: You thrive in cross-functional environments and have a natural ability to inspire open, purposeful communication with key stakeholders — building trust and fostering strong alignment across Engineering, Operations, Marketing, Quality, and Clinical Affairs. You act as a regulatory / quality expert and ambassador. /li /ul pbYour profile /b: /p ul liEngineer / Master degree (or equivalent) with a minimum of 7 years of significant experience in the Medical Device industry, preferably in orthopedics. /li liStrong knowledge of medical device regulations (specifically EU-MDR and FDA QMSR), associated standards and guidance documents. /li liDemonstrated experience in direct interactions with Competent Authorities and/or Notified Bodies, including the ability to prepare and defend regulatory positions and respond to technical objections. /li liSolid experience in problem solving and manufacturing change control (including RA Assessment) in the context of EU and US Regulations. /li liExperienced in compiling, submitting, and following up on technical dossiers, including 510(k) submissions. /li liKnowledge of risk management per ISO 14971:2019 and associated tools. /li liKnowledge of software-related regulatory requirements is an asset. /li liResults-oriented, with the ability to deliver on time and within defined scope. /li liAble to manage multiple projects and priorities in parallel, and to propose pragmatic solutions. /li liAnalytic, rigorous, autonomous, and collaborative. /li liClear communicator, able to adapt to different audiences while remaining factual and precise. /li liFluent in French and English; German is an asset. /li liPreferably located in French-speaking Switzerland. /li /ul /p #J-18808-Ljbffr