Experienced – Regulatory Compliance Specialist

Permitting and Regulatory Compliance SpecialistRIC Energy is seeking an experienced professional to oversee the permitting process for our renewable energy projects in Italy. As Head of Permitting, you will ensure compliance with national, regional, and local regulations, navigating complex regulatory landscapes and securing necessary permits to drive...

**Job Overview**We are seeking an experienced Regulatory Affairs Specialist to join our team at Cosmo Intelligent Medical Devices.

Merck Gruppe - MSD Sharp & Dohme is seeking a dedicated Regulatory Compliance Specialist to join our team.About the JobThe successful candidate will be responsible for ensuring compliance with ICH/GCP and country regulations, as well as company policies and procedures. They will act as the primary site contact and site manager throughout all phases of...

Company OverviewTN Italy is seeking a highly skilled and experienced Regulatory Affairs professional to join our team as Contractor Regulatory Manager.The successful candidate will be responsible for providing regulatory support and expertise to our clients, ensuring compliance with all relevant regulations and guidelines.Key Responsibilities:Initiate,...

About the PositionThe Senior Regulatory Affairs Specialist will play a critical role in maintaining Cosmo Intelligent Medical Devices' commitment to quality and safety. As a key member of our regulatory affairs department, you will be responsible for ensuring the compliance of our medical devices with regulatory requirements. This position requires an...

Regulatory Compliance OfficerDate posted: 12/01Location: Rome, ItalyCompany: WorldlineThis is WorldlineWe are the innovators at the heart of the payments technology industry, shaping how the world pays and gets paid. The solutions our people build today power the growth of millions of businesses tomorrow. From your local coffee shop to unicorns and...

Cosmo IMD is a division of the Cosmo Pharmaceutical group focusing on medical devices integrating artificial intelligence. Our team has developed expertise in various aspects related to AI MedTech business, such as medical device Hardware and Software design, healthcare Artificial Intelligence development, medical data harvesting, clinical development,...

Nuclear Regulatory Compliance SpecialistNtu International A/S participates in a consortium that is executing an EU-funded project to reinforce Egyptian nuclear safety and radioprotection regulatory infrastructure. To achieve this, the company seeks professionals to assist the core team during the project execution. The primary aim of this project is to...

About Cementir HoldingCementir Holding N.V. is a multinational cement company with a global presence in 18 countries across 5 continents.As one of the world's leading suppliers of cement, ready-mixed concrete, aggregates and concrete products, Cementir Holding has over 3,000 employees worldwide.Corporate Law Manager RoleWe are seeking an experienced...

Job SummaryWe are seeking an entry-level Regulatory Affairs Specialist to join our team. As a key member of our Regulatory Affairs department, you will be responsible for ensuring compliance with applicable regulations, guidelines, and standards.Key Responsibilities:Assess, prepare, and manage technical documentation to support certification and submission...

Job OverviewAt Cosmo Intelligent Medical Devices, we are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team. As a key member of our regulatory affairs department, you will be responsible for ensuring the compliance of our medical devices with regulatory requirements.About the RoleWe are looking for an experienced professional with...

Job SummaryZTE Italia is seeking a highly skilled and experienced Senior Legal Specialist to drive our company's growth and success.Main ResponsibilitiesThe successful candidate will be responsible for:Managing and overseeing legal assistance to various departments.Ensuring legal compliance across all business areas.Coordinating external legal advisors and...

About Meet Life Sciences and the RoleMeet Life Sciences is a leading organization in the life sciences industry, dedicated to delivering innovative solutions and services. We are currently seeking a skilled Regulatory Affairs Consultant to join our Italy affiliate team as a freelancer/contractor.Key Responsibilities:Support the development and implementation...

On behalf of our client - important pharmaceutical group - we are looking for a CMC Regulatory Senior Specialist Ensuring high quality contents for regulatory CMC documentation in line with applicable guidelines for new and approved Drug Products and/or Drug Substances of Company Group in Europe, USA and other countries.Key Responsibilities: Authoring of CMC...

**Job Summary**TN Italy is seeking a highly skilled Contractor Compliance Specialist to join our team in Rome. As a key member of our regulatory team, you will be responsible for ensuring compliance with relevant regulations and guidelines.**Key Responsibilities**Support the implementation of regulatory changes through Pfizer's enterprise system for changes...

The ideal candidate will have a strong background in regulatory affairs, with experience in managing vigilance reporting, risk management, and compliance. They will be able to work independently and collaboratively across multifunctional teams, and possess excellent analytical skills with a detail-oriented approach.

We are looking for a Medical Device Compliance Specialist to join our Regulatory Affairs team at JR Italy. The successful candidate will be responsible for ensuring compliance with EU regulations and guidelines.About the RoleThe Medical Device Compliance Specialist will be responsible for assessing and preparing technical documentation to support...

Job Title: Contractor Regulatory ManagerAbout the RoleWe are seeking an experienced Contractor Regulatory Manager to join our team in Rome. As a key member of the regulatory team, you will be responsible for ensuring compliance with regulatory requirements and supporting the development of new products.ResponsibilitiesInitiate, review, and approve regulatory...

Junior Regulatory Affairs Specialist of Cosmo Intelligent Medical Devices. Work Location: Rome – Italy – Viale Ostiense 131/L Key Responsibilities: Assess, prepare, and manage technical documentation to support certification and submission processes in the European Union and U.S.A. Prepare and manage technical dossiers for submission in other countries...

Junior Regulatory Affairs Specialist of Cosmo Intelligent Medical Devices. Work Location: Rome – Italy – Viale Ostiense 131/L Key Responsibilities: Assess, prepare, and manage technical documentation to support certification and submission processes in the European Union and U.S.A. Prepare and manage technical dossiers for submission in other countries...