Trainee - Regulatory Affairs
hace 7 días
CONTRATO FORMATIVO PARA LA OBTENCIÓN DE LA PRÁCTICA PROFESIONALREQUISITOS:HABER FINALIZADO ESTUDIOS EN LOS ÚLTIMOS 3 AÑOSNO HABER TENIDO UN CONTRATO DEL MISMO TIPO CON ANTERIORIDADWho we are?Veterinary medicine manufacturersVetpharma is the veterinary division of Chemo, part of the Insud Pharma group, providing Animal Health solutions. We are located in Barcelona, where the group was founded in 1977.In Vetpharma we are a highly qualified team.We have extensive experience in development, registration and marketing veterinary medicinal products, API's and nutraceuticals.Overview:Compiles and manages the Registration dossier or the Variation packages and coordinates the submission and follow up until product approval and launch or change implementation. Organizes regulatory information, logs and tracking.Active participation in product development.Responsabilities:To stay updated on changes in legislation and regulations and advises and gives interpretation on the potential impact to the product registration, marketing, manufacturing or development.Participate in the product development and regulatory strategy of the new products.Prepare, review and approve protocols and reports from CMOs or CROs.Compilation of required information for registration dossiers and variations according to European legislation.Registration submission and follow up with Health Authorities until product approval and launch.Coordination and preparation of Answers to deficiencies letters received from Health Authorities.Maintains regulatory files/database and chronologies in good order. Establish and maintain system for tracking changes in documents submitted to agencies.Qualifications:Education: University Degree in life sciences (Veterinary, Pharmacy, Chemistry or Biology). Master is a plus.Languages: High level of English is a must; Knowledge of other European language is also a plus.Experience (years/area): No experience is required.Specific Knowledge: Very good knowledge of general pharmaceutical legislation and regulations and registration dossier format content. Proficiency with standard software tools (Word, Excel, PowerPoint, Project, etc.).Travels: OccasionallyPersonal skills: good communication skills, teamwork, results-oriented, autonomous, creative, and entrepreneurialOur benefits Flexible start time from Monday to Friday (full-time). Life and accident insurance.️ Ticket restaurant Benefits and Savings Club. Training and language learning platform Wellness platform with unlimited free psychologist sessions Cabify transportation service for employee use Development plans, internal mobility policy. Many moreWhat will the Selection process be like? ️ Stay tuned to your phone and email The first thing we will likely do is contact you through one of the two channels. Prepare well We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. Wait for the result We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. Do you think this offer is not for you? Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting#InsudPharma #Challenger #Insuder #InsudTalentCOMMITMENT TO EQUAL OPPORTUNITIESThe InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.
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Regulatory Affairs Manager
hace 21 horas
Catalonia, España Hezuo Ltd A tiempo completoAs Regulatory Affairs Manager, you'll play a pivotal role in supporting the geographical expansion of a dietary supplement ingredient business. Based in Barcelona, you'll coordinate regulatory activities that ensure timely and compliant product registrations, authorizations, marketing & scientific communication across international markets, while providing...
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Regulatory Affairs Manager
hace 1 semana
Catalonia, España G&L Scientific A tiempo completoThis role can be based in either our Barcelona, Belfast or London Office. We work on a hybrid basis.Ready to dive into some seriously meaningful science? We're looking for a seasoned CMC Regulatory Affairs pro who loves complex challenges, global coordination, and shaping regulatory strategy for a high-impact vaccine portfolio. You'll step in as our Senior...
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Trainee - Regulatory Affairs
hace 5 días
Catalonia, España Vetpharma A tiempo completoCONTRATO FORMATIVO PARA LA OBTENCIÓN DE LA PRÁCTICA PROFESIONAL REQUISITOS: HABER FINALIZADO ESTUDIOS EN LOS ÚLTIMOS 3 AÑOS NO HABER TENIDO UN CONTRATO DEL MISMO TIPO CON ANTERIORIDAD Who we are? Veterinary medicine manufacturers Vetpharma is the veterinary division of Chemo, part of the Insud Pharma group, providing Animal Health solutions. We are...
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Trainee - Regulatory Affairs
hace 5 días
Catalonia, España Vetpharma A tiempo completoCONTRATO FORMATIVO PARA LA OBTENCIÓN DE LA PRÁCTICA PROFESIONALREQUISITOS:HABER FINALIZADO ESTUDIOS EN LOS ÚLTIMOS 3 AÑOSNO HABER TENIDO UN CONTRATO DEL MISMO TIPO CON ANTERIORIDADWho we are?Veterinary medicine manufacturersVetpharma is the veterinary division of Chemo, part of the Insud Pharma group, providing Animal Health solutions. We are located in...
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hace 1 semana
Catalonia, España Oxford Global Resources A tiempo completoOxford Global Resources is seeking a Global CMC Regulatory Affairs Manager Consultant to support as external contractor on behalf of Oxford a top leading pharma company to support headquartered in Barcelona through our consulting services division.Key Responsibilities:Provide CMC regulatory insight and advice to multidisciplinary teams, as well as CMC...
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Senior Regulatory Strategist
hace 1 semana
Catalonia, España G&L Scientific A tiempo completoThis role can be based in either our Barcelona, Belfast or London Office. We work on a hybrid basis.Ready to dive into some seriously meaningful science? We're looking for a seasoned CMC Regulatory Affairs pro who loves complex challenges, global coordination, and shaping regulatory strategy for a high-impact vaccine portfolio. You'll step in as our Senior...
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Regulatory affairs associate
hace 1 semana
Catalonia, España Vetpharma A tiempo completoWho we are? Veterinary medicine manufacturers Vetpharma is the veterinary division of Chemo, part of the Insud Pharma group, providing Animal Health solutions. We are located in Barcelona, where the group was founded in 1977. In Vetpharma we are a highly qualified team. We have extensive experience in development, registration and marketing veterinary...
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Regulatory Affairs Associate
hace 2 semanas
Catalonia, España Vetpharma A tiempo completoWho we are? Veterinary medicine manufacturers Vetpharma is the veterinary division of Chemo, part of the Insud Pharma group, providing Animal Health solutions. We are located in Barcelona, where the group was founded in 1977. In Vetpharma we are a highly qualified team. We have extensive experience in development, registration and marketing veterinary...
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Quality regulatory manager
hace 1 semana
Catalonia, España Elemed A tiempo completoTitle: RAQA Lead - Spain and Portugal Location: Barcelona, Spain Contact: The company Are you someone who has Iberia-wide regulatory experiences and are looking for the next step in your medical devices career at the EMEA level? Are you someone who likes to think creatively and prioritizes medical devices that are always accessible to patients and surgeons...
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Quality and Regulatory Director
hace 4 días
Catalonia, España ARTO A tiempo completoPosition Overview The Director of Quality and Regulatory Affairs will play a central role in defining and executing the organization's overall quality and regulatory roadmap. This position oversees the Quality Control, Quality Assurance, and Regulatory Affairs functions, ensuring that operations, systems, and products consistently meet applicable GxP and...