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Digital Quality Manager - Pathology Introduction Unilabs is the largest provider of medical laboratory diagnostics for prescribers and hospitals in Switzerland and employs around 800 people. Your Tasks As Digital Quality Control Manager Pathology, you will play a central role in shaping and...

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...

• Manage all aspects of multiple, large event projects from initial briefing to successful delivery and closing, including logistics and project content
• Cooperate with all teams assigned to an event and ensure adherence to the client's operational standards, tools and processes

Quality Manager for Diagnostic Imaging Departement (60% - 80%)...

• Plan and perform GMP/GDP Audits at Contract Manufacturing Organizations (CMOs) or Suppliers
• Prepare audit findings & reports and discuss potential impact on business

Work closely within the Global External Innovation & Business Development team to identify, assess, and advance in- and out-licensing opportunities....

Senior Organizational Change Lead, Senior Organizational Change Lead, Global MES: OCM / MES /GxP / Global system deployments / Strategic Change initiatives / German/ English Background: The global MES program is accountable for developing MES business strategies and the implementation of harmonized...

• You are responsible for quality related topics like change controls, deviations and complaints related to DS products at CMOs
• Define together with the CMO effective CAPAs and track the timely implementation

Validation & Documentation Engineer (M/F/X) – 100% Following recent acquisitions, Dec Group continues to accelerate its growth and expands its product range, particularly in the field of aseptic and containment filling lines and Isolators. As a leader in the design and production of powder...

The position as QC Bioassay Manager is responsible for leading a team of seven employees within the Quality Control department of AGC Biologics Heidelberg. This role entails the management and oversight of analytical testing of Bioassay Methods for Proteins and Nucleic Acids, including PCR, ELISA,...

• Own EU regulatory strategy for assigned programs from First-in-Human through pivotal development and marketing authorization.
• Serve as primary EU regulatory contact for cross-functional teams and provide clear, actionable regulatory guidance while ensuring compliance with regulatory requirements

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

• Ensuring compliance with applicable medical device software regulations and standards, including ISO 13485, ISO 14971, IEC 62304, IEC 62366 and IVDR
• Defining, maintaining, and governing software-related quality policies, procedures, SOPs, templates and lifecycle frameworks

In the role as _Global Head of CMO & Partner Management,_ you provide strategic, disciplinary, and operational leadership for global CMO, partner, vendor, and contract management, ensuring that all external collaborations operate within a robust, future-ready oversight framework and remain aligned...

In the role as _Global Head of Knowledge Hub_, you manage and integrate organizational units to transform distributed expertise into a well-structured, inspection-ready, and decision-driving global knowledge system. At the same time, you effectively engage with global regulatory authorities,...

In the position as _Global Head of Quality_ you will lead a global Quality organization and define productcentric quality strategies for established products, ensuring integration, lifecycle management, and reliable supply. You drive consistent execution and continuous improvement by embedding...

• 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

• Define clinical and technical requirements for online eye testing and centration
• Understand limitations and barriers and lead mitigation
• Drive product development and user validation
• Serve as interface between optometry experts, engineers and business units