Regulatory Affairs Specialist

Senior Regulatory Affairs SpecialistCK Group is seeking a highly skilled Senior Associate in Regulatory Affairs to join a global pharmaceutical company on a 12-month contract basis.About the CompanyOur client is a leading pharmaceutical company committed to unlocking the potential of biology for patients suffering from serious illnesses. They discover,...

Senior Regulatory Affairs SpecialistCK Group is seeking a highly skilled Senior Associate in Regulatory Affairs to join a global pharmaceutical company on a 12-month contract basis.About the CompanyOur client is a leading pharmaceutical company committed to unlocking the potential of biology for patients suffering from serious illnesses. They discover,...

Senior Associate Regulatory Affairs - UK & IrelandCareer Category: RegulatorySENIOR ASSOCIATE REGULATORY AFFAIRS - UK & IRELANDWe are seeking a highly skilled Senior Associate Regulatory Affairs professional to join our team in the UK and Ireland. As a key member of our regulatory affairs team, you will play a critical role in ensuring the timely submission...

Senior Associate Regulatory Affairs - UK & IrelandCareer Category: RegulatorySENIOR ASSOCIATE REGULATORY AFFAIRS - UK & IRELANDWe are seeking a highly skilled Senior Associate Regulatory Affairs professional to join our team in the UK and Ireland. As a key member of our regulatory affairs team, you will play a critical role in ensuring the timely submission...

Proclinical are recruiting for a Regulatory Affairs Associate to join a pharmaceutical organisation. This role is on a contract basis and is either located in Uxbridge or Cambridge. **Key Skills and Requirements**: - Familiarity in an administrative field within a corporate or similar setting preferably within a healthcare sector. - Educated to a degree...

CMC Regulatory Manager Job DescriptionWe are seeking a highly skilled CMC Regulatory Manager to join our dynamic team at Parexel. As a key member of our regulatory affairs team, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological...

CMC Regulatory Manager Job DescriptionWe are seeking a highly skilled CMC Regulatory Manager to join our dynamic team at Parexel. As a key member of our regulatory affairs team, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological...

CMC Regulatory Manager Job DescriptionWe are seeking a highly skilled CMC Regulatory Manager to join our team at Parexel. As a key member of our regulatory affairs team, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products.Key...

CMC Regulatory Manager Job DescriptionWe are seeking a highly skilled CMC Regulatory Manager to join our dynamic team at Parexel. As a key member of our regulatory affairs team, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological...

CMC Regulatory Manager Job DescriptionWe are seeking a highly skilled CMC Regulatory Manager to join our dynamic team at Parexel. As a key member of our regulatory affairs team, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological...

CMC Regulatory Manager Job DescriptionWe are seeking a highly skilled CMC Regulatory Manager to join our team at Parexel. As a key member of our regulatory affairs team, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products.Key...

Regulatory Affairs Consultant - Medical Device Regulatory LeadWe are seeking a highly skilled Regulatory Affairs Consultant to lead our medical device regulatory efforts. As a key member of our team, you will be responsible for overseeing key regulatory activities and providing strategic and tactical support on combination product portfolios.Key...

Regulatory Affairs Consultant - Medical Device Regulatory LeadWe are seeking a highly skilled Regulatory Affairs Consultant to lead our medical device regulatory efforts. As a key member of our team, you will be responsible for overseeing key regulatory activities and providing strategic and tactical support on combination product portfolios.Key...

Senior Regulatory Affairs ManagerWe are seeking a highly experienced Senior Regulatory Affairs Manager to join our team at Lifelancer. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with regulatory requirements and providing strategic guidance on regulatory strategies.Key Responsibilities:Develop and implement...

Senior Regulatory Affairs ManagerWe are seeking a highly experienced Senior Regulatory Affairs Manager to join our team at Lifelancer. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with regulatory requirements and providing strategic guidance on regulatory strategies.Key Responsibilities:Develop and implement...

Job SummaryGilead Sciences International, Ltd. is seeking a highly experienced and skilled Executive Director to lead the Global Regulatory Affairs and Labeling function. This role will be responsible for overseeing the development and implementation of global labeling strategies, ensuring compliance with regulatory requirements, and driving innovation in...

Job SummaryGilead Sciences International, Ltd. is seeking a highly experienced and skilled Executive Director to lead the Global Regulatory Affairs and Labeling function. This role will be responsible for overseeing the development and implementation of global labeling strategies, ensuring compliance with regulatory requirements, and driving innovation in...

CK Group is seeking a Senior Associate in Regulatory Affairs to join a global pharmaceutical company on a 12-month contract basis. **Company Overview** Our client is a leading pharmaceutical company committed to unlocking the potential of biology for patients suffering from serious illnesses. **Job Summary** We are looking for a Senior Associate to...

CK Group is seeking a Senior Associate in Regulatory Affairs to join a global pharmaceutical company on a 12-month contract basis. **Company Overview** Our client is a leading pharmaceutical company committed to unlocking the potential of biology for patients suffering from serious illnesses. **Job Summary** We are looking for a Senior Associate to...

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