Egészségügy, gyógyszeripar állások Külföldön lengyel nyelvtudással

• hivatalos papírügyek intézésében (kb. 5 hivatal)
• lakáskeresésben
• a család integrációjában (párok regisztrálása az országba, gyerekeknek óvoda, iskola keresése)
• illetve folyamatosan nyomon követjük jelöltjeink karrierjének alakulását
• stabil egzisztenciát és kiváló megélhetést kínál számukra

• Lead and oversee all clinical safety and vigilance processes for medical devices.
• Manage adverse event assessment and reporting in compliance with global regulations.
• Ensure accurate development and maintenance of RSI, CIP, and IB safety content.

• 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.

• 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.

• 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.

Provide expert leadership and oversight for all clinical safety and vigilance activities associated with Class II and/or III Medical Devices (MD), ensuring adherence to global regulatory requirements and internal standards throughout the product lifecycle....

• Unlimited Earning Potential: Keep 100% of your personal training income with no cap!
• Tiered Rent System: A supportive start to help you succeed.
• Free Promotion: Showcase your skills across PureGym platforms.
• Professional Image: Receive a complete 12-piece uniform at no cost.

This role reports to the FMC Corporation’s Global Regulatory Sciences group and is part of the Global R&D organization....

• Contribute to all phases of medical device development, from architecture concepts to design verification and design transfer
• Design and develop low-power medical embedded systems, with a strong focus on safety, reliability and regulatory compliance (IEC13485, IEC60601, ISOetc.)