Senior sales executive állások, munkák egészségügy, gyógyszeripar területen

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...

Önálló munkavégzés gyógytornászként...

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

Development EngineerDevelopment Engineer: System Development / Medical Technology / Verification / Laboratory / SAP / Simulink / German / EnglishProject: We are looking for a Development Engineer for our client, based in Rotkreuz.Background:We are part of the On-Market Subchapter. Our team...

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....

Provide in-line medical review of individual case safety reports (ICSRs) arising from Company clinical trials and other sources Determine or confirm the need for expedited reporting to regulatory agencies Ensure quality coherence and accuracy of case narratives Perform medical assessment of cases...

• Lead the Near Patient Program in Germany, ensuring high-quality, patient-centred, and compliant care delivery
• Act as the senior clinical voice supporting operational and strategic healthcare decisions

• Lead the Near Patient Program in Germany, ensuring high-quality, patient-centred, and compliant care delivery
• Act as the senior clinical voice supporting operational and strategic healthcare decisions

• Lead the Near Patient Program in Germany, ensuring high-quality, patient-centred, and compliant care delivery
• Act as the senior clinical voice supporting operational and strategic healthcare decisions

Head NPI Project Management (a)Elos Medtech is one of the world’s leading development and manufacturing partners for companies in the medical technology sector. With sites in Switzerland, Sweden, Denmark, Germany, China, and the United States, we specialize in the production of implants,...

• Plan and Conduct GCP Audits: Develop a risk-based audit schedule covering all relevant areas, including investigator sites, vendors, and internal processes, to ensure adherence to GCP guidelines
• Oversee Corrective and Preventive Actions (CAPA) specific to GCP (internal or external)

Create high-quality, scientifically accurate, and compliant content aligned with client objectives with guidance Build knowledge of therapeutic areas, client products, competitors, and industry regulations Adapt writing styles across various project types, formats and audiences Participate in...