Senior Regulatory Affairs Specialist
hace 3 semanas
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.We are looking for a Senior Regulatory Affairs Specialist to join Biopharma Regulatory department.What your responsibilities will bePrepare, review, and manage complex submissions and follow up of product registrations or any other regulatory activity, ensuring timeliness, accuracy, comprehensiveness, or compliance with regulatory standards.Communicate with affiliates, outside companies and Health Authorities.Represent the regulatory function on project teams as related to worldwide product registrations.Adapt licenses to current regulations.Maintain tracking of product registrations.Support other Departments, Affiliates and Third Parties in any required regulatory information.Create regulatory affairs policies and procedures.Who you areTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Bachelor's Degree in Life Sciences field is preferred.Minimum 2 years of related technical and/or regulatory experience in pharmaceutical industry or an equivalent combination of education and experience.Experience with applicable worldwide regulatory product registrations laws and regulations.Experience of eCTD/CTD submissions, and dossier lifecycle management.Advanced level of English.User of Microsoft Office tools.You are meticulous and detail-oriented.You have excellent communication and teamwork skills, as well as initiative and results orientation.What we offerIt is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.Information about Grifols is available at www.grifols.com. If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to applyWe look forward to receiving your applicationGrifols is an equal opportunity employer.Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h.Benefits packageContract of Employment: Temporary positionFlexibility for U Program: Hybrid
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Senior Regulatory Affairs Specialist
hace 3 semanas
España Grifols A tiempo completoSenior Regulatory Affairs Specialist Barcelona Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in...
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Senior Regulatory Affairs Specialist
hace 3 semanas
España Grifols, S.A A tiempo completoWould you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and...
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Senior Regulatory Affairs Specialist
hace 3 semanas
España Grifols A tiempo completoWould you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and...
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Regulatory Affairs Specialist- EBD
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist
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Senior Regulatory Affairs Director
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Regulatory Affairs Documentation Specialist
hace 3 semanas
España Grifols SA A tiempo completoWould you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and...
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España Ecolab A tiempo completoEcolab, Purolite Resins, the world leader in resin-based separation, purification and extraction technology, is seeking a Senior Regulatory Affairs Specialist. We manufacture products which help our customers around the globe, mainly in pharmaceutical and life science sectors, with technology which are critical to safe manufacture of their products. It’s...
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España Arxada A tiempo completoArxada is a global leader in specialty chemicals, committed to solving the world's toughest preservation challenges through innovative science. With a legacy of over a century, we strive to develop sustainable solutions that enhance the health and wellbeing of people, extend the life of vital infrastructure, and reduce ecological footprints. Sustainable...
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hace 7 minutos
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España AstraZeneca A tiempo completoThe Senior Regulatory Affairs Director (SRAD), Global Regulatory Strategy will be responsible for overseeing the development and implementation of global regulatory strategies for assigned products in the Cell Therapy Immunology area, with the intention of achieving successful registration and lifecycle management to serve patient needs.You will be...
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Regulatory Intelligence Specialist
hace 3 semanas
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Senior Regulatory Affairs Engineer
hace 3 semanas
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