Team állások, munkák egészségügy, gyógyszeripar területen

• Lead and coordinate the daily work of the Quality Control Assistant team 
• Ensure quality compliance during production through checks and documentation review 
• Identify, document, and escalate deviations and quality issues in cooperation with QA and Qualified Person 

Gyermekekkel és fiatal felnőttekkel való egyéni, csoportos megsegítés, személyiségfejlesztés, ill. a gyermekekkel foglalkozó szakemberek munkájának segítése tanácsadással. Nevelőszülők kiválasztásában, támogatásában való feladatellátás. Pszichológus team munkájában való részvétel....

• Working on the inpatient ward with responsibility for admitted patients
• Outpatient clinic work with your own patient list
• On-call and standby duties
• Work within radiotherapy (depending on agreement and competence/interest)
• Participation in multidisciplinary team conferences (MDTs) based on interest

• sürgősségi ellátásban részesülő betegek állapotának folyamatos monitorozása, az állapotváltozások korai felismerése
• betegfogadás, azonnali ellátási és orvosszakmai teendők elvégzése, a romló állapotok időben történő észlelése

• Literature reviews as requested by client epidemiologists using the best practice methodologies
• Literature search and preparation of Literature review report for Pharmacoepidemiology
• Perform peer Scientific & Technical Review

Monitors CSR’s performance on a daily basis, by taping, listening to, reviewing and evaluating calls...

• 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;

• Act as first point of contact for customers
• Manage group mailbox ensuring that all orders are placed and all inquiries are dealt in a timely manner
• Raise tickets for customer data updates
• Process credit notes as required relating to price or delivery discrepancies

• az intézményekbe érkező gyermek/fiatal beilleszkedésének, személyiségfejlődésének elősegítése segítése;
• részt vesz a lakásotthoni team, valamint a pszichológusi munkacsoport megbeszélésein, munkatársak számára szervezett szakmai programokon;
• krízisintervenció;

• 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

• 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

• 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.

• Responsible for receiving/downloading information from different channels and receiving voice calls for reporting safety information.
• Route information/safety reports to appropriate Department (e.g. medical information, quality assurance) as applicable.

• Receipt / Download / Accepting of cases from Document Exchange Tool or electronically (or any other source)
• Translation of all relevant European Non-English information from source documents to English (if required) and updating relevant fields in Standard Adverse Event (AE) form

• Módszertani javaslatok és ajánlások kidolgozása, szakmai anyagok előkészítése, egyeztetése
• Jó gyakorlatok összegyűjtése, új eljárásrendek bevezetésének indítványozása
• Kapcsolattartás, egyeztetés a szervezet más egységeivel

• Receipt / Download / Accept cases from Document Exchange Tool or electronically (or any other source)
• Translation of all relevant European Non-English information from source documents to English (if required) and updating relevant fields in Standard Adverse Event (AE) form

• Receipt / Download / Accepting of cases from Document Exchange Tool or electronically (or any other source)
• Translation of all relevant European Non-English information from source documents to English (if required) and updating relevant fields in Standard Adverse Event (AE) form

• Responsible for receiving/downloading information from different channels and receiving voice calls for reporting safety information.
• Route information/safety reports to appropriate Department (e.g. medical information, quality assurance) as applicable.

• Acting as a specialist within the team
• Acquiring marketing authorizations for medicines in line with SOPs, WIs, and relevant regulatory guidelines
• Maintaining existing marketing authorizations according to market specific requirements and internal procedures

• Conduct different types of monitoring visits (pre-study visits, site initiation visits, interim monitoring visits & close out visits)
• Develop and maintain site and investigator relationships to ensure clinical trials are managed efficiently