Jobs für quality engineer bei Basel

ppbOverview /b /p /p pOur client a global leading Medical Device Manufacture based near Basel, Switzerland is looking for Senior QA Engineer. This is an exciting role which involves life changing operations for the patients. /p pbResponsibilities: /b /p liMaintain the QMS in accordance with certification standards and ensure its evolution /li liLead quality...

ph3Quality System Engineer - Medical Devices /h3 pFor our client, a major pharmaceutical company based in Basel, we are looking for a Quality System Engineer- Medical Devices in the digital health technologies arena. Digital Health Technologies (DHTs), including those with medical device capabilities, are critical for enhancing patient value. To address the...

ulliServing as the single point of contact: for technical conversations with third party device manufacturers regarding design controls, risk management, and agreements. Act as the Subject Matter Expert (SME) on device requirements and technical nuances; also ensure these elements are appropriately integrated into study protocols and documentation....

ppLocation: /p pBasel, BS, CH, 4030 /p pFlexible Work Arrangement: Onsite /p pJob Category: SCM (Procurement, Logistics, Stores) /p pCareer Level: Professional /p pRequisition Id: 6058 /p h3bPosition Summary /b /h3 pJet Aviation is a global leader in business aviation, setting the standard for service and operational excellence across a worldwide network. As...

pTalentor International GmbH seeks an experienced Regulatory Affairs professional to lead device regulatory activities for medical devices and related products. You will coordinate design controls, risk management, and documentation across internal teams and external manufacturers. /ppResponsibilities include regulatory characterization, submission support,...

pITech Consult AG in Basel seeks a Quality System Engineer with 7+ years' experience in medical devices or pharma. You will drive regulatory identity work, support risk management, and oversee change control with third-party manufacturers. /ppThe role requires deep knowledge of CFR Part 820/CSV, MDR, CE Mark, and ISO 13485, plus strong documentation skills....

pRoche seeks a Quality System Engineer with DHT capabilities to support regulatory assessments, documentation reviews, change control, remediation activities, and knowledge transfer across the DEPCS group. The role focuses on integrating DHTs into Roche Pharma’s portfolio and ensuring compliance with global SOPs. /ppThe successful candidate will oversee...

pHealthcaremarketing is seeking an experienced Regulatory Quality professional to lead device requirements, regulatory assessments, and quality documentation across global programs. You will collaborate with Product Management, Design, and Operations to ensure compliance with ISO standards and regulatory expectations. /ppThe role requires 7+ years in...

pGi Life Sciences Basel seeks a dedicated Quality Systems Engineer consultant with 7+ years in medical device or pharmaceutical manufacturing. You will assess regulatory identity, manage technical documentation, and lead change control activities for DHTs under Roche SOPs. /ppStrong ISO 13485/IEC 62304 knowledge and CSV experience are required. That role...

ppRoche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, F. Hoffmann-La Roche AG in Basel, we are looking for a /p h3Quality System Engineer with DHT Technical Capabilities /h3 h3Background: /h3 pDigital Health Technologies (DHTs), including those...

JETZT BEWERBEN DRUCKEN LINK KOPIEREN pRoche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, F. Hoffmann-La Roche AG in Basel, we are looking for a /p ppbbQuality System Engineer with DHT Technical Capabilities /b /b /p /p pbBackground: /b /p...

pStiftung Weizenkorn is looking for an SCM Supplier Quality Engineer EMEA in Basel to ensure supplier quality and compliance. This role involves managing supplier audits, overseeing quality-related processes, and ensuring adherence to aviation regulations. /ppThe ideal candidate brings over 5 years of experience in aerospace, strong analytical skills, and a...

Quality System Engineer-Medical Devices : Software Engineering / Medical Device / Pharmaceutical Industry / GCP / GXP / ISO 14155 / ISTQB / ISO / IEC 27001/ CFR Part 820/CSV, MDR, CE Mark, 510(k)/ Clinical Investigations / Englisch Projekt: For our client, based in Basel, we are looking for a Quality System Engineer-Medical Devices ...

ph3Responsibilities /h3ulliServing as the single point of contact: for technical conversations with third party device manufacturers regarding design controls, risk management, and agreements. Act as the Subject Matter Expert (SME) on device requirements and technical nuances; also ensure these elements are appropriately integrated into study protocols and...

ppDigital Health Technologies (DHTs), including those with medical device capabilities, are critical for enhancing patient value. To address the varying measurement needs across our clinical trials, we partner with multiple third-party DHT manufacturers. While DHTs are necessary to provide critical evidence to support medical decision making, they add...

Position Overview Digital Health Technologies (DHTs) are becoming increasingly important for generating meaningful clinical evidence and improving outcomes for patients. Depending on the requirements of individual clinical studies, various digital solutions and connected medical technologies from external manufacturers are integrated into the...

**Seniority Level** Mitarbeiter **Berufskategorie** Elektro & Mechanik **Stellenprozent** 100 % **Jobtyp** Temporär **Referenz-Nr.** AFE-EM-T-54604 ### **Beschreibung** ### As a first-tier supplier to our renowned business partner F. Hoffmann-La Roche Ltd. in Basel, we are currently looking for a motivated and dedicated **Quality System Engineer with...

The Perfect Candidate: Quality engineering expert with 7+ years of experience in the medical device or pharmaceutical industry. They possess deep expertise in digital and medical device regulatory activities (CFR Part 820/CSV, MDR, CE Mark, 510(k)), including evidence generation and submission development. They have a proven track record of leading,...

0 Teilen Wir sind eine Gruppe von Personalberatern, die sich ganz bewusst auf das Erbringen von Personaldienstleistungen in ausgewählten Fachbereichen konzentriert. Wir arbeiten kundenorientiert und kennen die Bedürfnisse und Anliegen von Partnern und Mitarbeitenden. Wir vermitteln und verrichten im sprichwörtlichen Sinne gute Arbeit. Für unseren Kunden,...

Quality Control Manager (m/w/d) Wir sind eine Gruppe von Personalberatern, die sich ganz bewusst auf das Erbringen von Personaldienstleistungen in ausgewählten Fachbereichen konzentriert. Wir arbeiten kundenorientiert und kennen die Bedürfnisse und Anliegen von Partnern und Mitarbeitenden. Wir vermitteln und verrichten im sprichwörtlichen Sinne gute...