Development állások XXIII. kerületben (egészségügy, gyógyszeripar)

• Ensure and update accurate product data in the company database in accordance with current regulations;
• Request price quotes and handling related communication with suppliers;
• Verify and enter the incoming data into the Abacus database;
• Perform related administrative tasks and documentation;

• Utilize clinical information in safety database to provide company causality assessment and comment.
• Review case reports for medical accuracy, including validation of adverse event listedness and coding consistency.
• Request follow-up information for robust case causality assessment.

• Lifecycle management of approved regulatory files
• Documentation support in registration and renewal procedures
• Preparation of ASMF/DMF/CEP according to project timelines, ensuring compliance with regulatory requirements and facilitating submissions to the Authorities

• represent Dürr Dental as product specialist responsible for hygiene and dental care (prophylaxis) products
• regular visits to dentists and dental hygienists, perform demonstrations and product trainings

• Identify, interpret, and extract adverse event information from source documents.
• Receive, triage, and book‑in ICSRs from email and other sources.
• Process non‑serious and serious AE/ADR cases in global safety databases in line with SOPs.

• Continuously gather and analyse the latest medical and scientific information related to our HIV and Oncology products, therapeutic areas, and competitors.
• Deliver scientific presentations to healthcare professionals, medical societies, and other relevant audiences.

Working directly with customers and project teams providing technical expertise on Veeva’s applications, Vault Platform, APIs, and Java SDK Developing custom code and configuring Veeva software Contributing to solution design under guidance of experienced technical and migration architects...