Junior software developer állás, munka

• Leading and advancing chromatographic methods for the characterization of active ingredients, pharmaceuticals, and excipients
• Ensuring robust analytical results with a focus on content determination, degradation products, stability profiles and degradation pathways

• In-process controls, release and stability tests using HPLC-based analytical methods 
• DLS-based analyses; pH, IR, and wet chemical analyses
• Visual appearance test of finished drug product for batch release and stability 

• 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

Subject-Matter Expert (SME) for Test Method Development of delivery devices and combination products: Test Method development, including best practices for universal implementation, Test Method Validation/Transfer....

• 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.

define medical communication and messaging concepts for assigned therapeutic areas based on customer insights, medical developments, and competitive monitoring in relevant markets, including consideration of trends in patient care...

• Coordination of the (partial) project to establish and continuously expand the EU reference network with all participating centres and clinics at EU level
• Participation in the helpdesk for the network's eHealth service
• Work with the project management team on the progression of the clinical registry

• 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...

• 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.

• 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.

• 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

• 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).

• Advising our customers by providing product and application expertise as well as technical support in the area of fluid management
• Supporting the sales department in analyzing customer requirements and customer processes (incl. identification of optimization opportunities)