...receipt Diversity & Inclusion / EEO
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Role Requirements
Essent...
...RA DOC REGULATORY ASSISTANT
Barcelona, Spain
Hybrid
CL 11 - temporary contract // contrato en prácticas
Do you enjoy being surrounded by regulatory related information and documents? Is so, this is th...
...OTC.
As we expand our portfolio and increase our international presence, we are looking for an experienced International Portfolio Manager within the Global Regulatory Team in Headquarters located in Barcelona.
...
...implementation experience and a passion for helping customers optimize their regulatory data and document management process. As a key member of our Professional Services team, the Senior Consultant will be responsi...
...We are looking for a Regulatory Affairs Manager- Medical Devices with experience within the medecth and/or pharmaceutical industries and team management to join us, someone who loves to take on new challenges, to wo...
JOIN THE TEAM
In addition to its own products, BASF Española S.L. markets more than 5,000 products from the BASF Group: chemical, organic and inorganic products, catalysts; phytosanitary products, plastic materials, dispersions and raw materials ...
...Technology (BIST) and the “Xarxa de Centres de Recerca de Catalunya” (CERCA). We’re currently on the lookout for an International Talent Officer to join our People and Academic Affair team. You will work closely wit...
...following changes in AML and Regulatory Compliance risk assessments. - Act as advisor on CDD related queries from the Compliance Team members (both 1LOD and 2LOD) and the wider business. - Conduct Due Diligence chec...
...Regulatory Affairs Analyst & VIE page is loaded Regulatory Affairs Analyst & VIE
Apply locations Barcelona time type Full time... ...mind and work is driven by our shared values: be coura...
...functions on regulatory requirements and assigned business processes.
Acting as a subject matter expert during audits and inspections (e.g. FDA and EMA), leading the preparation of responses to findings and the d...
