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• Lifecycle management of approved regulatory files
• Documentation support in registration and renewal procedures
• Preparation of ASMF/DMF/CEP according to project timelines, ensuring compliance with regulatory requirements and facilitating submissions to the Authorities

• Working on the inpatient ward with responsibility for admitted patients
• Outpatient clinic work with your own patient list
• On-call and standby duties
• Work within radiotherapy (depending on agreement and competence/interest)
• Participation in multidisciplinary team conferences (MDTs) based on interest

Implementation of new features within the Veeva Quality suite at Life Sciences companies Solutioning and configuration of Vault applications to meet customer needs, including workflows, document types, security, fields, page layouts, notifications Collaboration with customer's business and IT staff...

• Contributing to the development and execution of strategy
• Developing the external opportunity funnel: Identify, evaluate, and execute internal and external growth opportunities via strategic partnerships, investments, M&A
• Execute and manage strategic projects

Working directly with customers and project teams providing technical expertise on Veeva’s applications, Vault Platform, APIs, and Java SDK Developing custom code and configuring Veeva software Contributing to solution design under guidance of experienced technical and migration architects...

• Aufbau starker Beziehungen zu wichtigen Entscheidungsträgern durch regelmäßige Kundengespräche, Präsentationen und strategische Account‑Betreuung.
• Einführung und Ausbau der Nutzung des diagnostischen Portfolios von Hologic durch effektives Upselling und lösungsorientierte Beratung.

Implementation of new features within the Veeva Quality suite at Life Sciences companies Guidance on enhancing quality and compliance culture through Veeva Quality suite Design of customer-requested and proactive solutions Customer liaison and communication management between implementation,...

Project Manager We are Sonic Suisse Sonic Healthcare operates a network of regional laboratories across Switzerland through Sonic Suisse, employing more than 2,500 people. Together, we make an important daily contribution to laboratory medicine and healthcare services. We offer a meaningful working...

• Maintenance and calibration of equipment.
• Homogenization of the samples (Most of our samples are fruit and vegetables).
• Organizing and managing the storage of samples and waste.
• Implementation of quality assurance measures.
• Participating in the improvement, development and validation of methods.

• Lead Reporting: Create FVL P&L statements, market and business analysis, and financial and operational performance reports.
• Performance Analysis: Analyze business performance, identify pain points, and make proactive improvement suggestions.

• You lead the strategy and roadmap for our enterprise eHealth portfolio, including cloud and platform solutions.
• You own and manage the full product lifecycle, from concept and MVP to launch, scaling, and end of life.

• Manage and maintain Safety Data Sheets (SDS)
• Support regulatory documentation and compliance activities
• Maintain internal databases and digital systems
• Help improve workflows and data quality
• Collaborate with international teams on sustainability and compliance topics

You will begin your work with an in-depth analysis of the current state of research and lay the strategic foundation for the project by comprehensively researching and evaluating diverse assay technologies, from innovative recognition molecules to advanced coupling and detection strategies....

• People management for members of the Mechanical Engineering team, including people development and recruitment
• In collaboration with the Engineering leadership, ensure correct staffing of projects

• Drive the development of brand and disease area strategies for the INT region, aligned with corporate and portfolio goals.
• Act as the primary marketing partner for affiliates, fostering a strong, collaborative international marketing community.

REGEDENT AG is a Swiss company headquartered in Zurich/Switzerland. Thanks to many years of experience in the fields of regenerative and implant dentistry, REGEDENT offers high-quality, customer-tailored products and solutions, enabling profession-als to improve their patients’ health and quality...

• Lead the end-to-end management of clinical studies for Class III medical devices, from feasibility assessment through study close-out
• Develop, maintain, and track clinical project plans, timelines, budgets, and risk management strategies

Operational Problem Solving: Dive deep into operational opportunities across Customer Care and Medical Ops, identifying root causes of challenges & pain points across the customer journey through rigorous analysis and data-driven insights...

Direct management of Process Team Leaders: Oversee and develop the Process Team Leaders and, indirectly, their respective teams in vaccine production...

Research Associate (Biology, 100%, m/f/d) NBE-Therapeutics is a subsidiary of the Boehringer Ingelheim group (BI): a perfect symbiosis between a rapidly growing biotechnology company and an already well-established big pharma. We are located in Basel, a Swiss city on the river Rhine, known for...