Regulatory Excellence Specialist

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 OverviewWe are seeking a highly skilled Regulatory Document Specialist to join our team at VCLS. As a key member of the team, you will be responsible for creating high-quality medical documents for various client projects.The ideal candidate will have a strong background in regulatory affairs and excellent writing skills. You will work closely with...

OverviewMRA Search has been appointed by a rapidly expanding, Hong Kong-based asset management company to find a highly skilled Regulatory Compliance Specialist for their Cambridge office. This will be the firm's first UK Compliance hire and will suit candidates with a strong interest in crypto/web3.SalaryThe salary for this position is estimated to be...

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...

Key Role in UK Regulatory AffairsA key position has become available in our UK location for an EU Regulatory Affairs Specialist. As a vital member of our team, you will play a crucial role in supporting the preparation and submission of regulatory documentation for marketing authorization applications in the UK.Main Responsibilities:Preparation and...

Gilead Sciences is a global biopharmaceutical company that is committed to making a difference in the lives of people with life-threatening diseases. We are seeking a highly skilled Senior Medical Writer to join our dynamic team. As a Senior Medical Writer, you will be responsible for authoring complex regulatory documents, including clinical study reports,...

Job Title: Regulatory Affairs SpecialistEstimated Salary: $80,000 - $110,000 per annumAbout UsWe are a leading multinational pharmaceutical company based across global locations. Our mission is to accelerate access to affordable and innovative medicines.Job DescriptionThe successful candidate will be responsible for preparation and submission of UK MAA...

Job Title: Regulatory Affairs SpecialistAbout Us:Dr. Reddy's Laboratories is a leading multinational pharmaceutical company based globally with over 24,000 employees.We accelerate access to affordable and innovative medicines for better health outcomes worldwide.Location: Dr. Reddy's (UK) Ltd, Cambridge (UK)Job Description:This role involves the preparation...

Welcome to Vivify Talent LimitedWe're a small consultancy with big ambitions, seeking an experienced Regulatory Document Specialist to spearhead key documents and projects. As a fully remote role, you'll enjoy autonomy and flexibility while collaborating with our passionate team.Your Key ResponsibilitiesDevelop top-tier regulatory documents, ensuring...

Quality Management Position: We are seeking an experienced Quality Specialist to join our team at 52North - creators of Neutrocheck ®. The successful candidate will play a key role in managing our Quality Management System (QMS), ensuring compliance with regulatory requirements, and supporting the development of our medical devices.Job Summary:The Quality...

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 Title: Compliance OfficersEstimated Salary: $85,000 - $110,000 per year.Bicycle Therapeutics is a pioneering pharmaceutical company dedicated to developing innovative treatments for complex diseases. As a Senior Associate in Regulatory Affairs, you will play a critical role in shaping the company's regulatory strategy, ensuring compliance with global...

About the JobWe are seeking an experienced Regulatory Affairs Specialist to join our team at ProductLife Group in the UK. As a key member of our regulatory affairs division, you will play a crucial role in ensuring compliance with UK and European regulations for nutrition and health products.Responsibilities:Review product formulations and labels to ensure...

Cpl Life Sciences is seeking a highly experienced Lead Regulatory Affairs Specialist to join our team in Cambridge, UK. This is a unique opportunity to work with a prestigious global drug development consultancy business that specialises in supporting pharma, biotechs, spin-outs, and academic groups with drug development activities.The successful candidate...

We are seeking an experienced Regulatory Affairs Specialist to join our team at Vertex Ventures HC. In this role, you will play a critical part in ensuring the regulatory compliance of our cancer therapies.As a key member of our Regulatory Affairs team, you will be responsible for developing and executing global regulatory strategies for assigned programs or...

Job OverviewWe are seeking a highly skilled Regulatory Compliance Specialist to join our team at Marshall Motor Group. This is a temporary opportunity to cover Maternity Leave, offering a unique chance to make a significant impact on our compliance framework.

About the Apprenticeship OpportunityIn partnership with TOPRA, we are offering a unique chance for recent graduates to gain hands-on experience in Regulatory Affairs. As part of this 30-month programme, you will receive comprehensive Regulatory training and work closely with experienced Consultants and clients from the pharmaceutical and medical device...

About the OpportunityWe have an exciting opportunity for a Senior Associate, Regulatory Affairs, CMC who is passionate about advancing therapeutics against life-threatening diseases. In this role, you will provide CMC regulatory support for new marketing applications and post-approval regulatory filings across international regions.As a key member of our...

Regulatory Affairs Job Opportunity in Dr. Reddy's LaboratoriesWe are looking for a talented EU Regulatory Affairs Specialist to join our team in Cambridge, UK. As a key member of our Regulatory Affairs team, you will be responsible for supporting the preparation and submission of regulatory documentation for marketing authorization applications in the...

Company OverviewBicycle Therapeutics is a pioneering pharmaceutical company pushing the boundaries of innovation in drug development. Our mission is to create life-changing therapies for underserved diseases.About the RoleWe are seeking a skilled Senior Associate, Regulatory Affairs to join our team. As a key member of our regulatory department, you will be...