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- CartaMundi is looking for a SAP FICO expert willing to join our Global Applications team!CartaMundi is looking for a SAP FICO expert willing to join our Global Applications team!
- CartaMundi is looking for a SAP SD expert willing to join our Global Applications team!CartaMundi is looking for a SAP SD expert willing to join our Global Applications team!
- Voor de klant Janssen Pharmaceutica is AUSY op zoek naar een Procurement Officer. Dit is een uitdagend functie in een leuke werkomgeving waar teamwork bovenaan staat!Voor de klant Janssen Pharmaceutica is AUSY op zoek naar een Procurement Officer. Dit is een uitdagend functie in een leuke werkomgeving waar teamwork bovenaan staat!
- The internship opportunity:In the department of Dossier Development and Operations we currently have an internship position for a CMC Regulatory Dossier Writer (m/f). In this internship you will have the opportunity to participate with one or more project development teams on breakthrough medicines for unmet patient needs.Job description:The CMC Regulatory Dossier Writer is a key member of CMC pharmaceutical development teams responsible for writing CMC sections of regulatory submissions and managing responses to related Health Authority (HA) questions. The Dossier Writer uses their scientific knowledge and communication skills, in conjunction with strong project management skills, to drive the timely completion of high-quality submissions across the portfolio in Janssen R&D. He/she works closely with functional representatives (i.e., Analytical, Drug Product Development, API synthesis/manufacturing, Portfolio Management, Quality, Clinical Supplies, CMC Regulatory) to gather data and presents the appropriate information in a clear and concise manner that supports HA approval and advances the development and commercialization of medical products.The internship opportunity:In the department of Dossier Development and Operations we currently have an internship position for a CMC Regulatory Dossier Writer (m/f). In this internship you will have the opportunity to participate with one or more project development teams on breakthrough medicines for unmet patient needs.Job description:The CMC Regulatory Dossier Writer is a key member of CMC pharmaceutical development teams responsible for writing CMC sections of regulatory submissions and managing responses to related Health Authority (HA) questions. The Dossier Writer uses their scientific knowledge and communication skills, in conjunction with strong project management skills, to drive the timely completion of high-quality submissions across the portfolio in Janssen R&D. He/she works closely with functional representatives (i.e., Analytical, Drug Product Development, API synthesis/manufacturing, Portfolio Management, Quality, Clinical Supplies, CMC Regulatory) to gather data and presents the appropriate information in a clear and concise manner that supports HA approval and advances the development and commercialization of medical products.
- Voor de klant Janssen Pharmaceutica is AUSY op zoek naar een administratief bediende. Dit is een uitdagend functie in een leuke werkomgeving waar teamwork bovenaan staat!Voor de klant Janssen Pharmaceutica is AUSY op zoek naar een administratief bediende. Dit is een uitdagend functie in een leuke werkomgeving waar teamwork bovenaan staat!
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