Junior software developer állás, munka

Following up on production-related nonconformities, supporting root cause analyses, defining and monitoring corrective actions, and preparing evaluations and statistics of nonconformities...

• Develop and implement of medical strategies and tactical plans for Hematology focus areas
• Initiate and execute tactical measures in alignment with the medical strategy
• Build and maintain in-depth expertise in Hematology
• Conduct product-related medical training for internal stakeholders

• Multiple years of experience in field sales in a similar environment
• The fundamental ability to successfully lead a field sales team
• A first experience as a regional manager would be beneficial
• Excellent knowledge of our markets and products as well as our partners' sales products

In this role, you will take the lead in developing Pharmaceutical Drug Products (New Chemical Entities - NCE), guiding the process from lead candidate selection through formulation and process development to the manufacturing of clinical trial materials. Additionally, you will support packaging...

• Collect data and prepare progress reports, KPIs, and metrics for regional and global reporting, including monthly reports, management reviews, and quarterly quality reports.
• Support ad hoc global quality reporting by gathering data and providing contextual insights to regional QA Senior Management.

• Perform analyses of finished products, samples in progress, raw materials, excipients, cleaning samples, validations and environmental monitoring according to established procedures.
• Ensure the maintenance and proper functioning of the BCQC laboratory equipment.

Szociális asszisztensi feladatok ellátása az 1993.évi III. törvény és az 1/2000.(I.7.) SZCSM rendelet alapján; valamint az 1997.évi XXXI. törvény és a 15/1998.(IV.30.) NM rendelet alapján....

Act as the Regional Business Process Owner for GMP/GDP Quality Assurance processes related to Change Control and Risk Management within the EUCAN region....

• Serve as the Regional Business Process Owner for GMP/GDP Quality Assurance processes related to Complaint Management and Recall within the EUCAN region.
• Lead the regional standardization and harmonization of Complaint Management and Recall processes, ensuring alignment with GMP and GDP requirements.

• Serve as the Regional Business Process Owner for GMP/GDP Quality Assurance processes related to Deviation, CAPA, and OOx within the EUCAN region.
• Drive the standardization and harmonization of these processes at a regional level, ensuring alignment with both GMP and GDP requirements.

• Lead complex, data-driven engagements with international healthcare stakeholders
• Design and own project frameworks, KPI models, scoring methodologies, and implementation roadmaps in close collaboration with the Analysis and Data Science teams

• You ensure that each batch is manufactured and tested in accordance with legal regulations
• You approve or reject bulk and finished products and sign the corresponding test protocols
• You approve specifications, sampling instructions, and testing instructions and ensure compliance with them

• Support MED-EL rehabilitation services world-wide
• Provide content and manage the hearing rehabilitation portfolio
• Develop and promote rehabilitation materials, tools, programs, and services for various platforms and media

• take over a wide range of analytical and research tasks, support in the creation and updating of presentations as well as sales support materials and assets
• work on one dedicated sales enablement project, assisting in project management, and content creation

• Responsible for the functionality, data quality, compliance, and user-friendliness of RIMS and eCTD systems.
• Ensuring the operation, maintenance and further development of the systems (Extedo eCTDmanager, Veeva RIM).