Regulatory Affairs Manager

Oatly, the original oatmilk company, is expanding its presence in North America and seeks a highly skilled Regulatory Affairs Manager to join our team. As the leader of our US-based regulatory affairs function, you will provide expert guidance on food law and compliance matters.About the Role:This role involves leading the Oatly North America Regulatory...

Regulatory Manager Job DescriptionThe Regulatory Manager provides regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures, ensuring timely preparation of well-organized, quality regulatory submissions in compliance with applicable...

About the RoleWe are seeking a highly experienced Senior Regulatory Affairs Officer to join our team at QbD Group in Spain. As a key member of our regulatory affairs department, you will be responsible for ensuring compliance with pharmaceutical legislation and regulations.With a strong background in regulatory affairs, you will have expertise in ICH...

Job SummaryThe Senior Regulatory Affairs Manager will oversee the Regulatory Affairs group in assigned regions, ensuring services are conducted according to Innovaderm's standard operating procedures, applicable regulations, and good clinical practices. This role requires leadership on regulatory activities, planning, and assigning work, overseeing direct...

Regulatory Manager Job DescriptionThe Regulatory Manager provides regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures, ensuring timely preparation of well-organized, quality regulatory submissions in compliance with applicable...

Regulatory Manager Job DescriptionThe Regulatory Manager provides regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures. This role ensures timely preparation of well-organized, quality regulatory submissions in compliance with...

Regulatory Manager Job DescriptionWe are seeking a highly skilled Regulatory Manager to join our team at Precision for Medicine (CRO). The successful candidate will provide regulatory strategy and development guidance for optimal conduct of clinical trials, ensuring timely preparation of well-organized, quality regulatory submissions in compliance with...

Unlock Your Potential in Regulatory AffairsWe are seeking a highly experienced Senior Regulatory Affairs Manager/Consultant to join our team at Parexel. As a key member of our regulatory affairs team, you will be responsible for managing client relationships, developing regulatory strategies, and ensuring compliance with EU guidelines.Key...

About the Role:The Regulatory Affairs team at QIAGEN is seeking a qualified professional to take on a management role, alongside a Senior Manager. The ideal candidate will have experience in a regulated industry, with participation in Regulatory Affairs activities preparing FDA submissions and EU Technical Documentation.Key Responsibilities:Regulatory...

Regulatory ManagerThe Regulatory Manager plays a critical role in ensuring the compliance of clinical trials with applicable regulations. This includes providing regulatory strategy and development guidance, coordinating and preparing regulatory documents for submission to Regulatory Authorities and/or Ethics Committees, and maintaining a current knowledge...

Key Responsibilities and Accountabilities:Global Regulatory LeadershipThe Global Regulatory Affairs Lead provides global regulatory leadership of assigned programs, developing global regulatory strategies, including risk assessment and mitigation strategies. This role chairs a Global Regulatory Team (GRT) of regulatory Subject Matter Expert(s) and is the...

Regulatory Affairs SpecialistJohnson and Johnson is seeking a skilled Regulatory Affairs Specialist to join our team in Madrid. This role offers a hybrid working model and is an exciting opportunity to contribute to our company's mission to build a world where complex diseases are prevented, treated, and cured.Key ResponsibilitiesSupport the growth of our...

Regulatory Affairs SpecialistAs a Regulatory Affairs Specialist, you will play a critical role in ensuring the compliance of our clinical trials with regulatory requirements. Your responsibilities will include providing regulatory guidance throughout the clinical development life cycle, compiling and coordinating applications to Regulatory Authorities, and...

Regulatory Affairs InternAt Kenvue, we are committed to delivering high-quality products that meet the highest standards of safety and efficacy. As a Regulatory Affairs Intern, you will play a critical role in ensuring compliance with regulatory requirements and maintaining our competitive edge in the market.Key Responsibilities:Regulatory Affairs:...

Quality Assurance and Regulatory Affairs ManagerMADRIDQuality Assurance- Requirements:As a Quality Assurance and Regulatory Affairs Manager at Mcr International, you will participate in the implementation of a total quality culture in the company, ensuring full company compliance with MDR, ISO 13485, and 9001 requirements, and internal quality manuals,...

We are seeking a talented Regulatory Affairs Intern to join our team at Kenvue. As a Regulatory Affairs Intern, you will play a key role in ensuring the compliance of our products with regulatory requirements in Spain.Key Responsibilities:Coordinate and submit new drug applications, cosmetics, medical devices, food supplements, or similar products to...

We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Ventós Group. As a key member of our international company, you will be responsible for maintaining our product database, collaborating in the homologation of new products and suppliers, and preparing technical documentation for our products.As a Regulatory Affairs Specialist,...

About the Role:We 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 Responsibilities:Develop...

Regulatory Affairs Specialist Role:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Ventós Group in Sant Just Desvern, Barcelona. As a Regulatory Affairs Specialist, you will play a key role in maintaining our product database, collaborating with suppliers to homologate new products, preparing technical documentation, and...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Alk-Abelló A/S. As a key member of our regulatory team, you will be responsible for handling CMC documentation for products manufactured at our site in Madrid, ensuring compliance with local and regional requirements.Key Responsibilities:Coordination and...