Medical device Jobs

CMC Technical Writer – DP Drug Product Lyophilization (M/F)

Basel, Basel-Stadt

...device, biotechnology, nutrition, and activities in clinical operations, regulatory affairs, quality, biometrics, pharmacovigilance, and HEOR. J-18808-Ljbffr
vor 24 Tage in Jobleads

Laborant/in Qualitätsprüfung (m/w/d) 80-100%

Muttenz, Basel-Landschaft

...Device Regulation) von Vorteil. Arbeitserfahrung in einem regulierten Umfeld. Beherrschung der MS Office-Palette. Genauigkeit, Zuverlässigkeit...
vor 24 Tage in Jobleads

Global Product Manager, Surgery

medmix Haag, St. Gallen

...Bioengineering, Business or a related field. 5+ years of product management experience in medical device industryExperience in B2B marketing and/or sales
vor 15 Tage in Whatjobs

Quality Engineer

Le Locle, Neuenburg

We are currently looking for a Quality Engineer to support one of our clients in the medical device industry. The ideal candidate will provide quality...
vor 25 Tage in Jobleads

Quality Engineer

Le Locle, Neuenburg

We are currently looking for a Quality Engineer to support one of our clients in the medical device industry. The ideal candidate will provide quality...
vor mehr als 1 Monat in Jobleads

System Engineer

TN Switzerland Chur, Graubünden

...of regulatory requirements and the medical device development lifecycle. Fluent in written and spoken English and German – at least B2 level. J-18808-Ljbffr
vor 18 Tage in Jobgoal

System Engineer (6295)

CTC Resourcing Solutions Chur, Graubünden

...device development lifecycle. Fluent in written and spoken English and German. Would you like to learn more about CTC and the opportunity outlined? Please...
vor 19 Tage in Jobgoal

System Engineer

Chur, Graubünden

...of regulatory requirements and the medical device development lifecycle. Fluent in written and spoken English and German – at least B2 level. J-18808-Ljbffr
vor 17 Tage in Jobleads

Quality Expert R&D and Global Engineering (m/w/d) * Stelle b

SCHOTT Pharma Schweiz Sankt Gallen, St. Gallen

...device-, or pharma industry with development environment and contact to QMS acc. To ISO 15378 or ISO 13485 or similar Diligence, proactive and structured...
vor 22 Tage in jobscout24.ch

Quality & Regulatory Approval Specialist (f/m/x) with German

Zug, Zug

...medical devices). Knowledge of ISO 13485:2016, ISO 9001:2015. Understanding of Good Distribution Practices. Very good German and English language knowledge...
vor mehr als 1 Monat in Jobleads

Senior Clinical Trial Specialist

Yverdon-Les-Bains, Waadt

...clinical studies, from planning activities to archiving of study documentation. Its main role is to set-up clinical investigations for Symbios medical...
vor 10 Tage in Jobleads

Data Engineer

Zürich, Zürich

JOB DESCRIPTION: Thoratec Switzerland GmbH is part of the medical device division of Abbott Laboratories, a fortune 500 company with over 115’000 employees...
vor 27 Tage in Jobleads

Software Development Engineer C+ RT (m/f/d)

Hays Zug, Zug

...level: Associate Employment type: Contract Job function: Engineering and Information Technology Industries: Medical Equipment Manufacturing #J-18808-Ljbffr
vor mehr als 1 Monat in Jobgoal

Design control specialist combination product

Basel, Basel-Stadt

...opportunity to play a key role in an expanding team and contribute to impactful projects within the drug-device combination product space. J-18808-Ljbffr
vor mehr als 1 Monat in Jobleads

Clinical Studies Technician (6 months)

Chéserex, Waadt

...device manufacturing establishment. Demonstrate ability to analyse information in a structured manner and to be able to prepare coherent technical reports...
vor 11 Tage in Jobleads

Junior Product Management and Planning Lead (m/f/d)

unisite Aesch, Basel-Landschaft

...provider in the field of Employer Branding & Talent Management. We provide consulting services to clients in the chemistry, pharmaceutical, biotech, medical...
vor mehr als 1 Monat in Jobgoal

Regulatory Affairs Specialist

Carouge, Genf

...device and drug experience essential. Including relevant experience in new product development and strategic understanding of registration processes...
vor mehr als 1 Monat in Jobleads

QARA MAnager

Neuenburg, Neuenburg

...medical device industry, with at least 2 years in quality management. Expert knowledge of ISO 13485, MDSAP, ISO 14971, and MDD/MDR (2017/745). J-18808-Ljbffr
vor 9 Tage in Jobleads

Senior Mechanical Engineer

Job Description Barrington James' specialist R&D division are currently recruiting for a Senior Mechanical Engineer to work for a Medical Device organisation...
vor mehr als 1 Monat in Jobleads

Strategic Buyer - Medics

Zürich, Zürich

...procurement improvement Work closely with internal teams (clinics, procurement managers) to ensure cost optimization Oversee compliance with relevant medical...
vor mehr als 1 Monat in Jobleads

R&D Engineer

Lausanne, Waadt

...device industry regulations (FDA, MDR, ISO 13485 and ISO 14971). Rigor, attention to details, dedication, self-driven, and sense of responsibility. Ability...
vor mehr als 1 Monat in Jobleads

Sustaining Engineering Group Leader

Electro Medical Systems S.A. Nyon, Waadt

Press Tab to Move to Skip to Content Link EMS is a global leader in the design, manufacturing, and sale of devices used for medical and dental treatments...
vor 10 Tage in Jobgoal

Production Supervisor

Genf, Genf

...Includes, but not limited to: Maintains operational objectives aligned with corporate policies and goals Supervises in the medical...
vor 10 Tage in Jobleads

Quality, Regulatory, Clinical Affairs Manager (20~40%)

Lausanne, Waadt

...Regulatory, Clinical Affairs Manager (20~40%) 06.01 2025 Quality, Regulatory, Clinical Affairs Manager (20~40%) COMPANY DESCRIPTION Emovo Care is a medical...
vor mehr als 1 Monat in Jobleads

Junior Platform Software Developer

Ziemer Ophthalmic Systems

...level Entry level Employment type Full-time Job function Engineering and Information Technology Industries: Medical Equipment Manufacturing #J-18808-Ljbffr
vor mehr als 1 Monat in Jobgoal