Riporting manager állások, munkák egészségügy, gyógyszeripar területen

• A piaci információk alapján a portfólióba tartozó gyógyszerek éves forgalmának előrejelzése a gyártók felé
• Forecast alapú rendelési és készletgazdálkodási döntések meghozatala
• Új gyógyszerek bevezetésének irányítása, belistáztatás, árazási stratégia kialakítása

• Szakmai tanácsadás és telepi auditok: állategészségügyi és takarmányozási ajánlások kidolgozása, termelési problémák megoldása.
• Termékportfólió szakmai támogatása: vakcinák, gyógyszerek, takarmány-kiegészítők alkalmazási protokolljainak kidolgozása és bevezetése.

• Üzleti kapcsolatok kialakítása és fenntartása GMP-releváns beszállítókkal
• EU GMP és Viatris minőségügyi rendszerek betartásának biztosítása
• Gyártási dokumentációk és változtatási kérelmek felülvizsgálata
• Kivizsgálások és reklamációk lezárásának felügyelete

• QM tervezése és nyomon követése a telephelyre vonatkozóan
• QMS stratégia kidolgozása, illetve megvalósítása
• Oktatási stratégia kidolgozása/megvalósítása
• Lean folyamatok kialakítása
• PQR folyamatának fejlesztése
• Minőségellenőrzési rendszer folyamatfejlesztése
• VMP rendszer fejlesztése

• Lead the commercial development of profitable lab testing services
• Lead and develop the lab organization
• Monitoring of the laboratory and all work carried out there, to ensure compliance with relevant internal procedures and regulations

• Ensure Data Management activities comply with internal standards and regulatory requirements (e.g., ICH-GCP)
• Support the development and testing of (e)CRFs and data review tools
• Contribute to the creation and maintenance of Data Management documentation

• Conducting sales calls and meeting with key decision makers to introduce/upsell our entire portfolio of products.
• Building rapport with existing clients and new.
• Ensure fast implementation and execution of strategies, projects and methods.

Serve as the labeling lead for all global labeling matters, ensuring regulatory‑compliant, current, and competitive core labeling documents (CDS, BPL, BSS)....

• Start Date: 16 February 2026
• Latest Possible Start Date: 16 March 2026
• Planned Duration: 12 months
• Extension: Very likely (approved budget)
• Location: Rotkreuz
• Workload: 100%
• Home Office: Yes, less than 50%
• Team Size: 28 people
• Department: Design Control Excellence CH (DSRSPC)

• Play an important role within in a multidisciplinary team in the development of new and complex products / segments / features and in the management throughout the entire life cycle
• Create product visions and/or strategies independently for complex products / segments / features

Define and lead the global Clinical Affairs strategy for Brainlab's global surgery portfolio, ensuring alignment with product, regulatory and commercial objectives / teams...

As a Senior Product Portfolio Manager (f/m/x) within ZEISS Meditec AG, your role is similar to and in strong collaboration with product management for the single products contributing to your clinical workflow solution...

As a Product Portfolio Manager (f/m/x) within ZEISS Meditec AG, your role is similar to and in strong collaboration with product management for the single products contributing to your clinical workflow solution....

Create and/or hold scientific presentations, lectures, training courses, speaker decks, FAQ documents etc. with targeted content for the respective stakeholders...

Definition and implementation of the clinical evaluation strategy for complex and challenging development projects focused on innovative microsurgical applications in the area of intra-operative visualization and digital imaging in neurosurgery...

• Manage all lifecycle stages of M&A/PMI projects from the Service perspective, including both Due Diligence as well as Post-Merger Integration projects
• Develop and apply upside potential & risk scenario assessment frameworks for Service

• Product Management for electric-acoustic solutions and related objective measures
• End-to-end product lifestyle management: from requirements gathering and development support to launch activities and in-life management
• Delivery of presentations and training for employees, professionals, and recipients

• Develop and deliver global educational programs and materials (live and digital).
• Support planning and execution of international scientific initiatives (e.g. advisory boards, expert meetings).
• Coordinate adaptation of global materials for affiliates, ensuring scientific accuracy and brand alignment.

Cross-Disciplinary Roadmap Definition: Define and drive a comprehensive robotics roadmap that serves various clinical disciplines, ensuring long-term strategic alignment....

• Lead and develop the Product Risk Management team
• Own and continuously improve the risk management process according to ISOwithin our product development framework
• Ensure high-quality risk analyses and maintain consistent, audit-ready risk management documentation