Within this role you will provide regional regulatory support for multiple products. It is essential that you have STRONG strategy and recent EMA clinical experience. You will have a strong background supporting the diversity of regulatory procedures in the EU (inc. PIPs, variations, IMPDs, ...

My client is a leading pharmaceutical company based in the centre of Paris and they specialise in the development of human and veterinary medicine. Within this role you will gain exposure to extensive clinical development programs in oncology and in inflammatory and neurodegenerative diseases,...

A excellent opportunity has arisen for a Regulatory affairs officer to join a specialist pharmaceutical company based in West Sussex. Within this role you will be responsible for performing & reviewing regulatory affairs activities, including the maintenance of New Product Registrations and th...

An excellent opportunity has arisen for a Regulatory Manager / Team Leader to join a global team within a specialist Pharmaceutical company based on the south coast. Within this role you will gain a large amount of exposure working closely with R&D, QA and PV teams and lead a team of Regulatory...

An exciting opportunity has become available for an experienced and enthusiastic Regulatory Affairs Executive / Senior Regulatory Officer, to join an exciting new client based in Berkshire! The successful candidate will have a strong background in registration and post approval submissions, an...

An excellent opportunity has arisen for a Regulatory Associate to begin their Regulatory career within an exciting emerging pharmaceutical company based in Berkshire. The role of the regulatory affairs associate will be to support the team in the preparation and submission of applications, an...

An excellent opportunity has arisen for a Senior Regulatory Officer to join a global team within a specialist Pharmaceutical company based on the South Coast. Within this role you will gain a large amount of exposure working closely with R&D, QA and PV teams. The ideal candidate will have a ...

A brand-new opportunity has emerged to work for a rapidly expanding pharmaceutical company, who are wholly owned by a global pharma organisation with presence in over 40 countries and currently 8 manufacturing plants. Our client specialises in the manufacture of generic medicines and are gainin...

My client, an international biopharmaceutical company focussing within sleep and haematology/oncology, is currently searching for a Regulatory Affairs Director to join their team based in Oxfordshire. As the Regulatory Director, you will be key stakeholder in the company's regulatory activiti...

My client, a well established Oxford based Biopharma, currently seeks a CMC professional at Senior Manager / Associate Director level to join their team. Within this role you will be responsible for Global CMC and managing and leading registration and CMC regulatory support for commercial and ...

My client, a growing Pharmaceutical company based in Oxfordshire, is currently recruiting for a Regulatory Manager to join their team on an initial 12 month contract basis. The ideal candidate will have a strong clinical regulatory background with a large amount of experience coordinating Clin...

An excellent opportunity has arisen for a Senior Regulatory Officer to join a global team within a specialist Pharmaceutical company based on the South Coast. Within this role you will gain a large amount of exposure working closely with R&D, QA and PV teams. The ideal candidate will have a ...

An excellent opportunity has arisen for an experienced labelling consultant to join a growing team based in High Wycombe. This is an urgent requirement and the ideal person will be able to join as soon as possible! Responsibilities: -Manage the development of updates to Company Core Data She...

A excellent opportunity has arisen for a Regulatory affairs officer to join a specialist pharmaceutical company based in West Sussex. Within this role you will be responsible for performing & reviewing regulatory affairs activities, including the maintenance of New Product Registrations and th...

An excellent opportunity has arisen for a Regulatory Associate to begin their Regulatory career within an exciting emerging pharmaceutical company based in Berkshire. The role of the regulatory affairs associate will be to support the team in the preparation and submission of applications, an...

My client, an established Biopharma based in Oxfordshire is currently searching for an experienced Senior Manager Regulatory Affairs Labeling to join their team based in Oxfordshire. Within this role you will be responsible for regulatory support (both technical and operational) in the area of...

My client is a leading pharmaceutical company based in the centre of Paris and they specialise in the development of human and veterinary medicine. Within this role you will gain exposure to extensive clinical development programs in oncology and in inflammatory and neurodegenerative diseases,...

An excellent opportunity has arisen for a Regulatory Manager / Team Leader to join a global team within a specialist Pharmaceutical company based on the south coast. Within this role you will gain a large amount of exposure working closely with R&D, QA and PV teams and lead a team of Regulatory...

An exciting opportunity has become available for an experienced and enthusiastic Regulatory Affairs Executive / Senior Regulatory Officer, to join an exciting new client based in Berkshire! The successful candidate will have a strong background in registration and post approval submissions, an...

My client, a well established Oxford based Biopharma, currently seeks a CMC professional at Senior Manager / Associate Director level to join their team. Within this role you will be responsible for Global CMC and managing and leading registration and CMC regulatory support for commercial and ...

My client, an established Biopharma based in Oxfordshire is currently searching for an experienced Senior Manager Regulatory Affairs Labeling to join their team based in Oxfordshire. Within this role you will be responsible for regulatory support (both technical and operational) in the area of...

TMF Compliance Manager wanted for our Basel based client in the pharmaceutical sector. Your experience/skills: * 3+ years of work experience in a clinical development, several years in global clinical operations or systems management are of advantage * Competency of working independently an...

Credit Risk Business Analyst / Tester (US Gaap Impairment) wanted for our Zurich based client in the banking sector. Your experience/skills: * Working experience in a large bank in compliance with testing experience within impairment projects such as IFRS 9 and US GAAP * Expertise as a Busi...

An excellent opportunity has arisen for a Medical Writer to join a pharmaceutical company based in Paris, specialising in the discovery, development, and commercialisation of novel targeted therapies, including cancer, chronic inflammatory diseases and neurological degenerative disorders. You...

My client is a leading pharmaceutical company based in the centre of Paris and they specialise in the development of human and veterinary medicine. Within this role you will gain exposure to extensive clinical development programs in oncology and in inflammatory and neurodegenerative diseases,...