Quality System Engineer (m/f/d)

h3Quality System Engineer (m/f/d) /h3 pTechfirm Engineering is looking for a Quality System Engineer (m/f/d) to join our team in the french speaking part of, Switzerland. /p pIn this role, you will support the effective deployment, compliance, and continuous improvement of the Quality Management System (QMS) within a regulated medical and technical environment. /p pYou will contribute to quality system improvement initiatives, audit readiness, record management, CAPA, root cause analysis, regulatory documentation, and new product development activities. /p pWhat You Will Do: /p ul liSupport the effective deployment and application of Quality Systems across the organization. /li liPerform periodic checks and reviews to verify appropriate application of quality processes and procedures. /li liAct as a Records Coordinator, supporting record management activities and the creation, organization, and maintenance of archives. /li liSupport audit readiness and participate in internal and external audits. /li liAssist with the investigation, response, and remediation of site‑specific Quality System audit observations. /li liIdentify root causes of quality issues and develop appropriate corrective actions and recommendations. /li liSupport and follow up on CAPA and corrective action plans, ensuring timely and effective implementation. /li liLead or participate in Quality System improvement and continuous improvement initiatives. /li liUse quality tools, statistical methods, and data‑driven reports to support process capability and quality improvements. /li liIdentify opportunities for process changes and improvements where appropriate. /li liEstablish and maintain effective quality‑related communication to increase awareness and promote continuous improvement across the business. /li liSupport the implementation of new product development procedures and documentation. /li liReview regulatory and quality documentation to ensure compliance with applicable requirements. /li liCommunicate business‑related quality issues and opportunities to relevant stakeholders and management. /li liSupport compliance with applicable Health, Safety Environmental requirements, as well as company policies and procedures. /li /ul pWhat We Are Looking For: /p ul liBachelor's or Master’s degree in Quality, Engineering, Life Sciences, Medical/Technical field, or a related discipline. /li liPrevious experience in a medical, pharmaceutical, biotech, MedTech, or technical industry. /li liExperience in Quality Systems and Quality Management within a regulated environment. /li liPrevious experience with record management and quality documentation. /li liExperience supporting internal and external audits. /li liGood knowledge of CAPA, root cause analysis, corrective actions, and quality investigations. /li liExperience with continuous improvement and Quality System improvement initiatives. /li liAbility to work with quality data, statistical methods, and quality tools. /li liGood understanding of regulatory and quality requirements. /li liStrong documentation, organizational, and analytical skills. /li liGood knowledge of Microsoft Office and confidence working with computer‑generated reports. /li liStrong communication and stakeholder management skills. /li liRigorous, structured, and detail‑oriented approach. /li liAbility to work independently as well as within cross‑functional and multicultural teams. /li /ul pLanguages Requirements: /p ul liFrench: fluent. /li liEnglish: fluent. /li liValid Swiss/EU/EFTA work authorization. /li /ul pWhy Techfirm? /p pAt Techfirm Engineering, you will: /p pJoin a Swiss‑headquartered company with a multicultural and collaborative environment. /p pWork on impactful Life Sciences, MedTech, pharmaceutical, and industrial projects across Switzerland. /p pContribute to challenging Quality System and compliance projects in regulated environments. /p pCollaborate with international experts and multidisciplinary teams. /p pDevelop your expertise through challenging and meaningful assignments. /p pBe part of a company culture focused on respect, professional growth, and employee well‑being. /p pPlease note: only candidates with valid Swiss/EU/EFTA work authorization can be considered. /p ul libWork location /b 2000 Neuchâtel (NE) /li libWorkload /b 100% /li libEmployment start /b Immediately /li libEmployment duration /b Permanent /li /ul ul libQualification /b skilled /li libWork experience /b More than 3 years /li libEducation /b Bachelor’s degree from a university or equivalent /li /ul ul libFrench /b Orally : Very good knowledge Written : Very good knowledge /li libEnglish /b Orally : Very good knowledge Written : Very good knowledge /li /ul #J-18808-Ljbffr