Senior c developer állások Külföldön (egészségügy, gyógyszeripar)

Senior R&D Project ManagerJoin a Team Advancing Precision Surgery Through Advanced ImagingSamanTree Medical is a privately held Belgian–Swiss medical device company dedicated to improving precision in surgery through innovative imaging solutions. Headquartered in Liège, Belgium, with R&D in...

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

Lead the development and continuous evolution of the German TMTT marketing strategy, ensuring alignment with the European vision while tailoring approaches to local market dynamics, regulatory frameworks, and unmet clinical needs....

Senior Expert Regulatory Affairs - CMC/BiosimilarsShape CMC regulatory strategy for complex biologics in a fast-growing biotech environmentFor a fast-growing, internationally active biotech company focused on biosimilar development, we are currently looking for a Senior Expert Regulatory Affairs...

Senior Global Medical AdvisorBecome part of a vital chain and contribute to our common goal of making people's lives better. Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma...

Senior AI Engineer – Practice Systems & Clinical Intelligence (w/m)Ärztekasse Genossenschaft develops integrated software solutions for healthcare professionals, supporting medical practices with secure, efficient, and intelligent digital services. To scale and mature our AI capabilities within the...

Senior Industrialization Project ManagerDesign the machines that build the future of medical technologyBased in the Neuchâtel canton, our client is a highly innovative Swiss MedTech company with nearly 100 years of precision engineering expertise. Recognized worldwide for the quality of its...

Be part of a highly motivated team of event managers to implement our EMEA-wide (Europe, Middle East and Africa) event concepts and other activities...

Provide comprehensive In-patient clinical case management for a patient where they will be completing status reports upon admission and whilst the patient remains admitted to the provider....

Lead and coordinate the Site-Launch activities and associated teams for internal and external sites and development projects...

Quality Manager Global BiopharmaSteriles - QA Operations - CMO ManagementAre you an experienced Quality Operations professional (m/f/d) looking to take ownership in a global external manufacturing environment? Our client is seeking a motivated Quality Operations Manager to provide quality oversight...

• Strategic ownership and development of assigned key accounts
• Building and maintaining long-term relationships with senior stakeholders in Pharma and Biotech
• Development and execution of account strategies and account plans

Drive deep, trusted relationships with your customers' C-level executives and senior stakeholders, ensuring alignment between their business priorities and SAP's solutions....

Lead the development and execution of the product strategy and roadmap for our ABL800 portfolio, aligned with corporate strategy and unmet customer needs across key care settings and/or disease clusters....

• Develop and implement global regulatory pathways for product authorizations
• Oversee preparation and submission of regulatory documents to authorities

Senior Director Innovation & Science, Dietary SupplementsJoin dsm-firmenich as Senior Director Innovation & Science, Dietary Supplements and lead the end to end innovation agenda for our Dietary Supplements segment. Based in Kaiseraugst, you will guide a team of six experts, drive a high impact...

Global Brand Manager CardioMetabolics (Diabetes)About AbbottAt Abbott, our mission is simple and powerful: to help people live healthier, fuller lives. With a presence in more than 160 countries and over 114,000 colleagues collaborating worldwide, we are dedicated to advancing innovation across...

• Provide guidance on regulatory and quality requirements, including MDR and FDA requirements, for our in-house and our customer software projects
• Create technical documentation for our industry projects together with our software development teams

• Batch record review for API and bulk product for monoclonal antibody prefilled syringes
• Assessment and documentation of product deviations, OOS, and changes
• Quality oversight for relevant service providers, including CMO's, laboratories, technical operations and supply chain

Provide comprehensive In-patient clinical case management for a patient where they will be completing status reports upon admission and whilst the patient remains admitted to the provider....