Regulatory Affairs Expert

We are seeking a highly experienced Regulatory Affairs Expert to join our growing team at VCLS. This role is ideal for someone with 4+ years of experience in regulatory affairs and a strong background in Clinical Trial Submissions.The successful candidate will play a key role in driving forward regulatory processes, ensuring compliance, and contributing to...

Job OverviewWe are seeking a highly experienced Senior Director to lead our Regulatory Affairs team at Cpl Life Sciences. This role will provide strategic regulatory advice to clients, taking into account regulatory guidelines and available measures to facilitate regulatory input.Key Responsibilities:Lead client projects, providing expert regulatory guidance...

Job Description: Quality Assurance and Regulatory Affairs ExpertCompany Overview:Newton Colmore Consulting is a leading consulting firm in the medical devices industry, providing expert advice on regulatory affairs and quality assurance. We are committed to delivering high-quality services that meet the needs of our clients, and we are seeking a talented...

The Regulatory Affairs Expert will be responsible for shaping IWF's policy positions and achieving real-world change through legislation, regulatory frameworks, and industry practice. This involves leading policy development, researching and gathering evidence, extracting information and communicating it effectively, engaging with stakeholders, and...

Job Description:We are seeking a highly skilled Regulatory Affairs and Quality Assurance Expert to join our team at Newton Colmore Consulting in Cambridge. As a key member of our Quality Assurance and Regulatory Affairs department, you will be responsible for providing advice on product creation and improvement.Main Responsibilities:Product Creation: Advise...

About VCLSWe are a leading consulting firm offering expert regulatory services to the pharmaceutical and medical device sectors. Our team is dedicated to providing high-quality support to our clients, ensuring compliance with regulatory requirements.This 30-month programme is designed for recent graduates with an interest in medicines and a desire to build a...

Job SummaryWe are seeking an experienced Global Regulatory Affairs Expert to join our team at Gilead Sciences, Inc. This is a key leadership role responsible for defining and implementing regulatory strategies for multiple biopharmaceutical products across various therapeutic areas.About the RoleDevelop and execute global regulatory strategies for assigned...

OverviewCpl Life Sciences is seeking a Senior Director Regulatory Affairs to join our team. This role offers the opportunity to lead client projects, provide strategic regulatory advice, and ensure compliance with UK, EU, and US health authorities.About the RoleAs Senior Director Regulatory Affairs, you will be responsible for preparing regulatory submission...

Job OverviewMoonLake Immunotherapeutics seeks a highly skilled Global Regulatory Affairs Director to lead the development and implementation of innovative global regulatory strategies for sonelokimab lead indication(s).This role will be responsible for regulatory aspects related to product development and approval, aligning with the global business strategy...

Regulatory Affairs Director Job OverviewWe are seeking a highly skilled Regulatory Affairs Director to join our team at Lifelancer. As a key member of our organization, you will be responsible for developing and delivering innovative global regulatory strategies for sonelokimab lead indication(s).About the RoleThis is an exciting opportunity to work with a...

Job Title: Regulatory Affairs DirectorWe are seeking a highly skilled and experienced Regulatory Affairs Director to join our team at Bicycle Therapeutics. The successful candidate will be responsible for developing and executing global regulatory CMC strategy and submissions for assigned programs or projects.The ideal candidate will have extensive...

Job OverviewWe are seeking a highly skilled Senior Associate, Regulatory Affairs to join our team at Bicycle Therapeutics. As a key member of our regulatory affairs department, you will be responsible for the development, execution, and tracking of global regulatory submissions for assigned programs or projects.

Job DescriptionCompany Overview: Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT.We connect talent with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains. Our mission is to provide innovative solutions for businesses and professionals in the industry.SalaryThe estimated salary for this position...

Job SummaryWe are seeking a skilled Regulatory Affairs Specialist to join our team at Vectura Group. As a key member of our regulatory affairs department, you will play a crucial role in ensuring compliance with global regulations and guidelines for medical devices and drug-device combination products.Key Responsibilities:Lead regulatory activities across...

Job DescriptionWe are seeking a highly skilled Device Regulatory Expert to join our regulatory affairs team at Vectura Group. As a key member of our team, you will be responsible for ensuring compliance with global regulations and guidelines for medical devices and drug-device combination products.Key Responsibilities:Regulatory Leadership: Assume the role...

VCLS is seeking a highly skilled Regulatory Affairs Specialist to drive forward regulatory processes, ensure compliance, and contribute to innovative clinical trials. The ideal candidate will have 4+ years of experience in Regulatory Affairs, with a focus on Clinical Trial Submissions (CTS). They will possess a deep understanding of regional and local...

Join MoonLake Immunotherapeutics as an Associate Director of Regulatory Affairs to spearhead innovative global regulatory strategies for sonelokimab lead indication(s).About the RoleCreate and execute cutting-edge regulatory plans to drive product development and approval, aligning with the company's global business strategy.As a key member of our team, you...

At Gilead Sciences, Inc., we're seeking a highly experienced Regulatory Affairs Manager to lead our Global Regulatory team in the development and implementation of regulatory strategies for our Therapeutic Area (TA) portfolio. This role will oversee the preparation and submission of regulatory documents, as well as ensure compliance with global...

About GileadGilead Sciences, Inc. is a global biopharmaceutical company dedicated to developing innovative treatments for life-threatening diseases. We're looking for talented individuals to join our team as Regulatory Affairs Manager.Job DescriptionThis role will act as the Regional Regulatory Lead on complex or multiple products, compounds, indications or...

About the JobIn a continuous effort to grow and expand our services, ProductLife Group is looking for a Regulatory Affairs Specialist to join our team in the United Kingdom.This position plays a vital role in developing our local UK Regulatory Affairs presence, overseeing new regulatory activities related to the UK for multiple clients. You will work closely...