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Head of Service MED AT & CH (m/f/x) 100% Als Head of Service MED (m/f/x) CH & AT… Tragen Sie die Verantwortung für die Gesamtsteuerung der Serviceeinheit sowie für die fachliche und disziplinarische Führung der Servicetechniker...

We are looking for a creative, ambitious, and collaborative EARLY-CAREER RESEARCHER to establish an independent junior research group () in TRANSLATIONAL GYNECOLOGIC CANCER RESEARCH, FOCUSING ON EARLY DETECTION, DIAGNOSIS, THERAPY, OR PREVENTION OF OVARIAN AND/OR ENDOMETRIAL CANCER AND OTHER...

• Develop and execute regulatory strategies for products and services
• Provide regulatory expertise for complex or unique issues and challenges regarding registration and compliance activities.

• Management of the QC department, including responsibility for budget and personnel
• Ensuring the timely QC testing of relevant materials (e.g., raw materials, intermediates, drug substances, finished drug products)
• Responsibility for method qualification/validation

• Build, lead, and develop an international team to achieve sales and market development goals
• Own regional responsibility for ECMO business development in EMEA, Eastern Europe, and Latin America, including assigned product partners

• Line manager for the organization/project management of clinical studies in the Gastro II department
• Transfer of project responsibilities to assigned employees

• Are you passionate about nursing and looking for a change?
• Looking to apply your experience in a new environment?
• Is it time to move away from the demands of clinical care?
• Do you speak German and English?

• Are you passionate about nursing and looking for a change?
• Looking to apply your experience in a new environment?
• Is it time to move away from the demands of clinical care?
• Do you speak German and English?

Director MedTech Consulting & Business Development – Switzerland (m/w/d) seleon GmbH, a part of ai6 Solutions, is a leading service partner for medical technology companies in Central Europe for around 30 years, with a focus on development, regulatory consulting, and production. We support MedTech...

Onsite Associate Sample Management (m/f/d) Avantor is a global life sciences and advanced technology company providing mission-critical products and services to biopharma, healthcare, education, government, and applied materials industries. Onsite Associate Sample Management (m/f/d) Job description...

RESPONSIBILITIES: • Provide clinical care to students • Keep records in accordance with German law and regulations • Be aware of special needs, e.g. students with health issues and/or chronic conditions • Demonstrate familiarity with procedures in case of infectious diseases • Communicate...

Lead quality initiatives, processes and oversight of customer service / service recovery responses, in partnership with the in-country teams....

Intensive Educational Academy: Dive into a 12-month program that enhances your product knowledge, cardiovascular expertise, clinical understanding and fundamental commercial skills....

Provides medical input to Clinical Trial Protocol, Investigator's Brochure, Informed Consent Form, Independent Data Monitoring Committee Charter, Statistical Analysis Plan, Medical Monitoring Plan, Clinical Trial Report, Clinical Trial Overview Statements and other clinical trial documents...

• Serve as the primary contact for national and international customers in the field of medical devices and in-vitro diagnostics
• Manage and administer delivery and service contracts (e.g., MSA), including pricing, delivery terms, contract renewals, and amendments

Working independently in the areas of valve crimping, case management, pre-case planning, post-case management, 3 Mensio management, Therapy Awareness program management and clinical education programs...

Formulation Scientist vVARDIS is a Swiss-based oral health company founded by Dr. Haleh and Dr. Golnar Abivardi, dentists, innovators, and award-winning entrepreneurs. vVARDIS is the result of a combined 30 years of dental and entrepreneurial experience, and 20 years of laboratory and clinical...

• The DPL and IDT ensure that the project is advanced in a scientifically sound, efficient, and regulatory-compliant manner, with optimal use of resources
• The DPL should possess a broad, cross-functional skill set and act less as a subject matter expert (SME) in a single area

• Support clinical research, external science, and innovation decision-making through robust commercial assessments
• Act as the commercial counterpart to the Scientific New Products Team in all pre-commercial new asset processes

• Design and implementation of experiments investigating statistical learning and predictive processing using intracranial EEG and intracortical microstimulation in human epilepsy patients
• Analysis of intracranial electrophysiological recordings using modern computational and statistical approaches