We are searching for the best talent for a Regulatory Affairs Specialist to support the Manager of Regulatory Affairs in key duties and responsibilities, including providing RA support to achieve local registrations and market authorizations in the EMEA region, reviewing and appr ...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. · Providing RA support t ...

We are searching for the best talent for a Regulatory Affairs Specialist to support the Manager of Regulatory Affairs in key duties and responsibilities, including providing RA support to achieve local registrations and market authorizations in the EMEA region, reviewing and appr ...

We are on a mission to make all science open, enabling the research community to develop the solutions we all need to live healthy lives on a healthy planet. Frontiers is one of the world's largest and most impactful research publishers, dedicated to making peer-reviewed, quality ...

Regulatory Affairs Specialist responsible for supporting and executing regulatory activities across multiple projects and UCC and Surgery product lines to ensure compliance with industry standards and regulatory requirements. · Review and approve advertising and promotional mater ...

Regulatory Affairs Specialist responsible for supporting and executing regulatory activities across multiple projects and UCC and Surgery product lines to ensure compliance with industry standards and regulatory requirements. · Bachelor's degree in Life Sciences, Biomedical Engin ...

Support and execute regulatory activities across multiple projects and product lines to ensure compliance with industry standards and regulatory requirements. Review and approve advertising and promotional materials, manage regulatory and product related documentation, provide lo ...

Are you ready to launch your career in Regulatory Affairs and Quality Assurance, within a dynamic, international environment? · We're looking for a motivated and detail-oriented RA/QA Specialist to join our team in Madrid. · Execute daily Regulatory Affairs and Quality Assurance ...

We're seeking a highly experienced Principal Regulatory Affairs Specialist to lead regulatory strategy and ensure compliance and shaping market access and regulatory strategy across EMEA. · In this pivotal role, you'll drive global and regional regulatory processes, shape procedu ...

Are you ready to launch your career in Regulatory Affairs and Quality Assurance, within a dynamic, international environment? · We're looking for a motivated and detail-oriented RA/QA Specialist to join our team in Madrid. · Execute daily Regulatory Affairs and Quality Assurance ...

The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions. · This role will be responsible for s ...

As Global Regulatory Affairs Specialist - Labeling and Pharmacovigilance you will be responsible for the development and maintenance of Summary of Product Characteristics (SmPC), Patient Information Leaflets (PIL), packaging mockups, and advertising/promotional materials for medi ...

We're looking for a motivated and detail-oriented RA/QA Specialist to join our team in Madrid. You'll play a key role in ensuring our products and processes meet regulatory standards, support continuous improvement, and contributing to the smooth operation of our regional complia ...

We are looking for a Senior Regulatory Affairs Specialist to join our regulatory team in Spain. You will be responsible for ensuring the regulatory compliance of products and services for assigned countries and maintaining alignment with authorities, customers, and internal stake ...

We are looking for a Senior Regulatory Affairs Specialist to join our regulatory team either in France or Spain. · You will be responsible for ensuring the regulatory compliance of products and services for assigned countries and maintaining alignment with authorities, customers, ...

The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions. · ...

As Global Regulatory Affairs Specialist - Labeling and Pharmacovigilance you will be responsible for the development and maintenance of Summary of Product Characteristics (SmPC), Patient Information Leaflets (PIL), packaging mockups, and advertising/promotional materials for medi ...

The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions. · ...

We are looking for a Senior Regulatory Affairs Specialist to join our regulatory team either in France or Spain. You will be responsible for ensuring the regulatory compliance of products and services for assigned countries and maintaining alignment with authorities, customers, a ...

The Regulatory Specialist plays a key role in ensuring compliance with industry standards and regulatory requirements across multiple projects. · Maintain technical documentation repositories including Technical Data Sheet Instructions for Use Declaration of Conformity. · Address ...

About Changan · Changan Automobile, one of the world's leading automotive manufacturers from China, brings a rich heritage and global reach to the European market. With a presence in Europe since the early 2000s through design and R&D centers, Changan has now established its Euro ...