senior lead for regulatory projects - Barcelona - beBeeProjectManager

We are seeking a dynamic and experienced Regulatory Affairs professional to join our team asap. As an RA Project Manager, you will be responsible for a wide range of regulatory activities to support our company's third-party activities. · ...

Hetero Europe is seeking a dynamic and experienced Regulatory Affairs professional to join our team asap. As an RA Project Manager, you will be responsible for a wide range of regulatory activities to support our company's third-party activities. · ...

The Project Manager works as an integral part of the global Regulatory Affairs team to support the planning and execution of assigned Regulatory projects. · The role collaborates internally with colleagues in Medical Writing CMC publishing teams Medical Quality PV business develo ...

The Project Manager works as an integral part of the global Regulatory Affairs team to support the planning and execution of assigned projects. · ...

The Senior Project Manager, Regulatory Affairs works as an integral part of the global Regulatory Affairs team to support the planning and execution of assigned Regulatory projects... Flexible, inclusive culture — 70% remote workforce. · Bachelor's degree in life/health sciences ...

The Senior Project Manager works as part of the global Regulatory Affairs team to support planning and execution of assigned projects guiding cross-functional teams to deliver high-quality results within agreed timelines. · Supports the planning and execution of assigned projects ...

L'empresa busca un tècnic/a per cobrir un lloc amb discapacitat legalment reconeguda mínima o superior al 33 %, per evaluar seguretat/compliment regulatori d'ingredients i nous actius cosmètics. Experiència mínima de dos anys en comptes similars (cosmètica, química farma...), con ...

The Regulatory Affairs Specialist will be responsible for managing the regulatory lifecycle of US FDA-approved products. · ...

Shape the future of medicines with a global consultancy that values expertise energy and impact. G&L Scientific is a global regulatory consultancy with offices across three continents. We partner with some of the world's largest pharmaceutical and biotech companies while also sup ...

Gestor dirección solvencia en CaixaBank. · ...

We are seeking a Regulatory Operations Specialist to join one of our clients in the pharmaceutical sector based in Barcelona and offers a hybrid work model. · ...

Our client is a multinational leader in the manufacturing of high-quality packaging and industrial solutions. · Regulatory Compliance: Ensure all medical and surgical gloves comply with Spanish and EU regulations, including the preparation of documentation for the Spanish Agency ...

Sanofi Global Hub is an internal Sanofi resource organization based in India. · Main responsibilities: · ...

Manager Global Technology Transfer is responsible for leading end-to-end Technology Transfer execution providing Project Management, scientific and technical expertise. · ...

Principal Medical Regulatory Writer Location: Barcelona % of travel expected: Travel required as per business need Job type: Permanent and Full time · ...

We are seeking a Regulatory Operations Specialist to join one of our clients in the pharmaceutical sector. The position is based in Barcelona and offers a hybrid work model. As the Regulatory Operations Specialist, you will support our Regulatory Affairs department by contributin ...

The Solution Architect Regulatory & Compliance Applications will be responsible for the operation, optimization and continuous evolution of global regulatory IT solutions. · ...

Clinical Research Associate II conducts site management for clinical studies according to Fortrea's Standard Operating Procedures and ICH GCP Guidelines. · ...

We are seeking a hands-on Medical Writing Lead to own and operationalise our growing medical writing business. This is not a purely supervisory role; you'll be a do-er who can both run the business day-to-day and represent our expertise in client engagements. · ...

We are looking for a Quality Manufacturing Senior Specialist to join the Quality & Compliance area of a leading pharmaceutical company. · This role plays a key part in guaranteeing GMP compliance across operations involving CMOs, suppliers and external manufacturing sites. · The ...

++The Universal Kraft group has been actively developing renewable energy solutions for over 20 years.+ · +As Project Manager, you will be responsible for managing projects across their lifecycle,+from planning and execution through to delivery and close-out. ...