Junior software developer állások, munkák egészségügy, gyógyszeripar területen

• carry the Area Sales Manager responsibilities for assigned EMEA Distribution countries and all central charity organization projects in the region
• act as the Refractive Expert within the EMEA Distribution Partners team, supporting product positioning, training, and knowledge transfer

lead the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and company standards...

• pácinesek önálló vizsgálata, kezelése
• kezelési tervek felállítása
• egyéni, csoportos (igény esetén) terápiák vezetése
• kollégákkal és pácienssekkel való folyamatos kapcsolattartás
• szakmai elvárásoknak megfelelő dokumentáció vezetése

• Ensuring process adherence for the pre-market procedures
• Completeness of design history files and regulatory submissions
• Regulatory and process conformance for development and maintenance projects as a member of cross-functional teams

• identify, target, and develop new business opportunities with hospitals, clinics, diagnostic centers, and healthcare groups across the GCC
• increase the share of wallet within strategic accounts by promoting and expanding the existing product portfolio

• Leading the development of the faculty's research strategy and building a strong interdisciplinary team.
• Establishing translational research projects within SFU MED and in collaboration with national and international partners.

Munkakörhöz tartozó feladatok ellátása....

Munkakörhöz tartozó feladatok ellátása....

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

• Contributing to the research, development, verification, validation, and industrialization of our devices.
• Supporting the creation and implementation of design control, risk management, quality and regulatory documentation related to the devices and manufacturing processes.

• Provide organizational and administrative support to the Senior Commercial Director in daily operations
• Coordinate appointments, meetings, and travel arrangements
• Manage communication with internal and external stakeholders, especially healthcare professionals (HCPs)

• Drive regulatory strategy for new product launches, ensuring proactive and effective planning aligned with global requirements
• Lead a team of regulatory experts in External Devices & Software within Regulatory Affairs

Kardiológiai szakrendelésen a kardiológiai szakorvosi feladatok ellátása...

Bőrgyógyászati szakrendelésen a bőrgyógyász szakorvosi feladatok ellátása...

Szemészeti szakrendelésen a szemészeti szakorvosi feladatok ellátása...

• 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