Regulatory Affairs Manager: Thrive in a Dynamic Environment
hace 3 semanas
QbD Group is a knowledge-based company specializing in development, clinical, regulatory, and compliance services for the life sciences industry. Our team is dedicated to providing tailored solutions that meet the unique needs of our clients.
Salary and BenefitsWe offer an attractive and competitive salary package tailored to individual needs, taking into account local laws and regulations. In addition to a generous salary, we provide a range of benefits to support your personal and professional growth.
Job DescriptionAs a Senior Regulatory Affairs Officer, you will play a key role in ensuring compliance with pharmaceutical legislation and regulations, including GMP. Your expertise in ICH guidelines and registration dossiers, CTD format, project management, lifecycle management, price and reimbursement, and regulatory submissions will be instrumental in driving our success.
Required Skills and Qualifications- A Master's degree in Pharma Industry or Regulatory Affairs Management
- Minimum 4 years' experience in the field
- Strong analytical skills, attention to detail, and ability to manage multiple tasks and priorities
At QbD Group, we value our employees' contributions and celebrate their achievements. We offer a dynamic and supportive work environment, opportunities for continuous learning and development, and a chance to be part of our global success story. Our promise to you includes job security, lasting connections, and a joyful community where you can be yourself.
We stand for JPEG: Joy in Partnership, going for the Extra mile to Get things done. If you're interested in this opportunity, please submit your CV and motivation letter. We look forward to welcoming you to our QbD family.
-
Regulatory Affairs Manager
hace 3 semanas
Madrid, Madrid, España Oatly A tiempo completoOatly, 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 Affairs Professional
hace 3 semanas
Madrid, Madrid, España Johnson And Johnson A tiempo completoRegulatory 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 Specialist
hace 3 semanas
Madrid, Madrid, España Ventos A tiempo completoRegulatory 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...
-
Regulatory Affairs Manager
hace 3 semanas
Madrid, Madrid, España TRIUM Clinical Consulting NV A tiempo completoAbout 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...
-
Madrid, Madrid, España Parexel A tiempo completoOverviewWe are seeking a talented Clinical Regulatory Manager to join our dynamic team at Parexel. As a key member of our global regulatory affairs department, you will play a vital role in post-approval regulatory activities for biological products.
-
Regulatory Affairs Specialist
hace 1 mes
Madrid, Madrid, España Kenvue A tiempo completoRegulatory 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:...
-
Regulatory Affairs Strategy Specialist
hace 3 semanas
Madrid, Madrid, España Galderma A tiempo completoGalderma: A Pioneer in DermatologyWe are Galderma, a category leader in dermatology with a legacy that spans decades. Our innovative, science-based portfolio of premium brands and services addresses the full spectrum of the dermatology market through injectable aesthetics, dermo-cosmetics, and therapeutic dermatology.Unlock Your Potential with UsAt Galderma,...
-
Regulatory Affairs Professional
hace 4 semanas
Madrid, Madrid, España Groupe Productlife A tiempo completoAbout the RoleWe are seeking a skilled Regulatory Affairs Specialist to join our teams in Spain and contribute to the development of our local regulatory presence.Key ResponsibilitiesProvide guidance and support for managing submissions and requests from clients regarding Spain.Contribute to regulatory activities, including pre-licensing, new registration,...
-
Madrid, Madrid, España Mabxience A tiempo completoJob DescriptionThis is a highly specialized role for an experienced Regulatory Affairs professional, with expertise in biopharmaceuticals and biosimilars. You will be responsible for ensuring the adequacy of CMC documentation for global regulatory submissions, including regional registration processes.The ideal candidate will have broad knowledge of global...
-
Regulatory Affairs Specialist
hace 4 semanas
Madrid, Madrid, España Ergomed A tiempo completoAbout 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 Specialist
hace 3 semanas
Madrid, Madrid, España Johnson & Johnson Consumer A tiempo completoRegulatory 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 Expert
hace 1 mes
Madrid, Madrid, España Zentiva Group, a.s. A tiempo completoRegulatory Affairs Specialist RoleThe Regulatory Affairs Specialist at Zentiva Group, a.s. is accountable for managing the Regulatory Affairs agenda at country level within the company. This will include:Providing an efficient and proactive Regulatory service to meet the business objectivesSupporting the commercialisation of productsEnsuring agility in daily...
-
Regulatory Affairs Specialist
hace 3 semanas
Madrid, Madrid, España Iqvia A tiempo completoRegulatory 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...
-
Clinical Research Associate Director
hace 3 semanas
Madrid, Madrid, España Icon Plc A tiempo completo**Company Overview**ICON Plc is a world-leading healthcare intelligence and clinical research organization. We pride ourselves on fostering an inclusive environment that drives innovation and excellence, and we welcome you to be part of our mission to shape the future of clinical development.We are currently seeking a Clinical Research Associate Director -...
-
Regulatory Affairs Specialist Position
hace 3 semanas
Madrid, Madrid, España Zentiva Group, a.s. A tiempo completoJob 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...
-
Madrid, Madrid, España Tether Operations Limited A tiempo completoAbout Tether Operations LimitedAt Tether Operations Limited, we have been at the forefront of innovation since our inception in 2014. Our pioneering spirit has led to the development of groundbreaking technologies, including stablecoins, data platforms, and educational initiatives. With a commitment to pushing the boundaries of what is possible, we seek out...
-
Quality Assurance Specialist
hace 3 semanas
Madrid, Madrid, España Ferring Pharmaceuticals A tiempo completoJob 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...
-
Regulatory Affairs Specialist
hace 3 semanas
Madrid, Madrid, España Galderma A tiempo completoGalderma is a pioneering dermatology company with a rich legacy and commitment to innovation. With operations in approximately 90 countries, we deliver a diverse portfolio of premium brands and services that cater to the evolving needs of the dermatology market.We are seeking an expert Regulatory Affairs CMC Specialist to join our team in Barcelona. As a key...
-
Regulatory Affairs Professional
hace 2 semanas
Madrid, Madrid, España Johnson & Johnson Consumer A tiempo completoOverviewKenvue 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...
-
Regulatory Compliance Specialist
hace 4 semanas
Madrid, Madrid, España Tbwa ChiatDay Inc A tiempo completoJob Description: Tbwa Chiat/Day Inc is seeking a highly skilled Regulatory Manager to join our team. As a key member of the Precision for Medicine team, you will play a crucial role in providing regulatory strategy and development guidance for clinical trials.Key Responsibilities:- Provides regulatory guidance throughout the clinical development life cycle-...