Lider en Regulatory Affairs Biofarmacéutico

Descripción del puestoTu carrera comienza aquí: la beca DiscoveringYOU de AbbVie te da la oportunidad de desarrollarte en un entorno empresarial innovador y centrado en el paciente. Nuestro objetivo es ofrecerte la formación adecuada para enfrentar los desafíos del mundo laboral y contribuir a tu desarrollo profesional.Responsabilidades claveActividades...

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...

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...

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...

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...

About the RoleAs a highly skilled Regulatory Affairs Specialist, you will be responsible for ensuring the successful start-up and regulatory compliance of clinical trials. With your expertise in the pharmaceutical industry, you will play a key role in managing study start-up and regulatory deliverables.

Kenvue, a leading company in the pharmaceutical industry, is seeking a highly skilled Regulatory Affairs Professional to join its team in Madrid, Spain. As a key member of our regulatory department, you will be responsible for ensuring compliance with regulatory requirements and guidelines for new drug applications, cosmetics, medical devices, food...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team in Ergomed, a leading global clinical research organization. As a key member of our regulatory department, you will play a crucial role in ensuring compliance with regulatory requirements and facilitating the successful execution of clinical trials.

Regulatory Affairs InternWe are currently recruiting for a Regulatory Affairs intern at Kenvue. As a member of our global team, you will contribute to the development and implementation of regulatory strategies for our products. Your responsibilities will include coordinating and compiling new drug applications, cosmetics, and medical devices for submission...

Regulatory Affairs Role OverviewAs a Regulatory Affairs Specialist at IQVIA, you will play a critical role in supporting clinical trial and marketing authorization activities for both internal and external clients. Your expertise will be instrumental in preparing and reviewing regulatory submissions to ensure compliance with regulatory requirements.Key...

We are Bitfinex, a pioneering digital asset trading platform, and we are searching for a seasoned professional to join our Regulatory and Licensing team as a MENA Regulatory Affairs Manager. The ideal candidate will have a minimum of 5 years of experience in regulatory affairs within the financial services or crypto-asset industry. They will possess a deep...

Company OverviewTether Operations Limited is a pioneering company in the field of stablecoins and financial innovation. Founded in 2014, we have expanded our horizons into various business verticals, including Tether Data, Tether Power, and Tether Edu. Our mission is to create technological solutions that empower individuals, businesses, and governments...

Job OverviewVision Achievement is seeking an experienced Life Sciences Regulatory Affairs Specialist to join our team. As a key member of our consulting group, you will be responsible for planning and delivering life science consulting engagements related to quality and regulatory affairs infrastructure.

Job Title: Regulatory Affairs Specialist at EricssonAbout the Role:We are seeking a highly skilled Compliance Manager to join our team in Sao Paulo, Brazil. As a key member of our organization, you will play a crucial role in ensuring that we maintain the highest standards of compliance and regulatory adherence.About You:To be successful in this position,...

**Company Overview:** Vision Achievement is a leading provider of regulatory and quality consulting services to the life sciences industry. Our team is dedicated to helping clients navigate complex regulatory landscapes and achieve compliance with industry standards.**Compensation:** $85,000 - $110,000 per year, depending on experience and qualifications....

OverviewKenvue is a leading company in the healthcare industry, dedicated to delivering innovative products and services that improve people's lives. Our team is passionate about science and care, and we're committed to making a positive impact on the world.Job DescriptionWe're seeking a highly motivated and detail-oriented Regulatory Affairs intern to join...

En AbbVie, somos una empresa líder en el sector biofarmacéutico que se centra en el paciente y la innovación. Buscamos a un desarrollador senior que forme parte de nuestro equipo y contribuya a nuestro éxito.Sobre nuestra empresaAbbVie es una compañía biofarmacéutica dedicada al desarrollo de tratamientos avanzados para enfermedades graves y...

Exciting Opportunity in Regulatory AffairsCpl Healthcare is seeking an experienced Regulatory Affairs Director to lead our medical device lifecycle management efforts. This is a full-time, permanent position based in Madrid, Spain.About the RoleIn this role, you will be responsible for strategic lifecycle management of our medical devices post-CE approval...

Job Description: Ferring Pharmaceuticals seeks a Quality Assurance & Regulatory Affairs Specialist to support and contribute to the Quality and Regulatory Affairs team. Key responsibilities include managing the company's system of procedures, preparing and reviewing SOPs, and monitoring submitted variations to obtain approvals. Requirements:- Health Sciences...

Job DescriptionWe are seeking a skilled Regulatory Affairs Specialist to join our team at Zentiva Group, a.s. as part of our regulatory affairs department.About the RoleThis is a challenging and rewarding opportunity for an experienced professional to contribute to the company's success by ensuring compliance with regulatory requirements and guidelines. The...