Global Regulatory Affairs Lead

hace 5 días


España Sobi group A tiempo completo

Statistics show that women and underrepresented groups tend to apply to jobs only if they meet 100% of the qualifications. Sobi encourages you to change that statistic and apply. Rarely do candidates meet 100% of the qualifications. We look forward to your applicationAt Sobi, each person brings their unique talents to work as a team and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes from our team of people and our commitment to patients.Here at Sobi, our mission and culture get us excited to come to work every day, but here are a few more reasons to join our team:Competitive compensation for your workEmphasis on work/life balanceCollaborative and team-oriented environmentOpportunities for professional growthDiversity and InclusionMaking a positive impact to help ultra-rare disease patients who are in need of life saving treatmentsJob DescriptionKey Responsibilities and Accountabilities:Including, but not limited to the following:Single point of contact/single point of accountability within GRA on the Core Asset Team (CAT) and Medicines Development Team (MDT) for assigned program(s)Chairs a Global Regulatory Team (GRT) of regulatory Subject Matter Expert(s)Provides global regulatory leadership of assigned program(s)Develops global regulatory strategies, including risk assessment and mitigation strategies. Champions use of expedited regulatory pathways globally to accelerate patients’ accessAttends major/critical regulatory Agency meetings (US FDA, EMA/CHMP, PMDA, NMPA/CDE) for assigned program(s)May present to Senior Leadership regarding assigned program(s)Cooperates with other departments and affiliates within Sobi, regulatory authorities, partners and regulatory consultantsParticipates in strategic and regulatory evaluations of in-licensing mattersMay have direct oversight/management of Regulatory Affairs team members supporting assigned program(s)Authority to approve services and costs within budget and delegation from Sobi authorized signatoriesReview regulatory SOPs as neededParticipate in operational excellence work (improvement projects) as needed.Main contacts:Internal core interactions: All functions within Sobi, but in particular Commercial, Pharmacovigilance & Patient Safety, Supply Chain, Quality, Manufacturing & Supply, Clinical Development, Global Medical & Scientific Affairs, Project & Portfolio Management as well as Management Teams, Governance Teams and affiliates.External core interactions with: Regulatory Authorities, CROs, Consultants, Partners.May act as point of contact with US FDA or EMA.QualificationsDegree in Life SciencesExpert on all Regulatory Affairs processes, applications and regulatory environment to achieve and maintain marketing authorizationsGood knowledge of drug development and the rare diseases regulatory environmentExperience in haematology is preferredVery good knowledge in written and oral English, knowledge of other languages is an upside but not requiredAdditional InformationAll Sobi employees need to demonstrate behaviors in line with Sobi's core values: Care, Ambition, Urgency, Ownership and Partnership. Are you ready to be on the Sobi team? Come join a culture that empowers every person to be the person that makes a difference for rare disease.Why Join Us?We are a global company with over 1,700 employees in more than 30 countries and are committed to the societies where we operate. With a deeply skilled management team directing our day-to-day wins, and a Board with a stellar track record, we’re ready to take on the world’s diseases, ailments and adversity. Our people believe they have the power to make a positive impact in others’ lives because that’s exactly what we do here. If you’re seeking a career that taps into your talents in a way that makes the world a better, healthier place, we just may have a job for you.We know our employees are our most valuable asset, and our culture conveys that. We offer a competitive benefits package, to support the health and happiness of our staff.Sobi CultureAt Sobi, we refuse to accept the status quo. This is because we have witnessed first-hand the challenges facing those affected by rare diseases, and have used this knowledge to shape our business to find new ways of helping them.As a specialized biopharmaceutical company, we are dedicated to rare diseases. And we see this focus as a strength. By effectively turning our research into ground-breaking treatments, we help make medicine more accessible and open up more possibilities for patients and more opportunities for those caring for them. This has been our approach since day one, but we know we can’t change the world of rare diseases on our own. Accomplishing this requires strong partnerships with patients, partners and stakeholders across the entire value chain. Together, we define how our business can create solutions that serve the needs of those affected by rare diseases while facilitating sustainable growth.An Equal Opportunity EmployerSobi is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at Sobi are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity, protected veterans and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status or protected groups by the laws or regulations in the locations where we operate.Sobi is an affirmative action and equal opportunity employer. Disabled/Veterans. If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to use or access this website to apply for a vacancy as a result of your disability. You can request reasonable accommodations by sending an email to florencia.mendez@sobi.com.
#J-18808-Ljbffr



  • España Precision Medicine Group A tiempo completo

    Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific...


  • España AstraZeneca A tiempo completo

    The 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...


  • España Galderma Pharma S.A A tiempo completo

    Regulatory Affairs Associate With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that spans the full spectrum of the fast-growing dermatology...


  • España Sandoz A tiempo completo

    As Regulatory Affairs Associate Director, you will lead associates within Regulatory API (RAPI), accountable for driving and delivering high quality documentation supporting successful submission, within agreed timelines and project planes. Including preparation of registration documentation and assessment of appropriateness of registration documentation for...


  • España Global Life Science Hub A tiempo completo

    Global Life Science Hub has partnered with a one-of-a-kind, global CDMO that specializes in providing comprehensive development and manufacturing services. With an additional 50% growth expected in Europe site, we’re searching for a Regulatory Affairs Associate who will manage the relationships with key suppliers and build your own technical specialization...


  • España Cpl Healthcare A tiempo completo

    Job Title: Associate Director, Regulatory Affairs - Medical Device/Post-Market SurveillanceJob Type: Full Time, Permanent PositionLocation: Spain, Madrid – HybridRemuneration: Attractive salary and packageAn exciting opportunity to join a growing pharmaceutical company that specializes in Cancer and Supportive Care, Gastroenterology, and Hepatology. Due to...


  • España Galderma A tiempo completo

    With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that spans the full spectrum of the fast-growing dermatology market through Injectable...


  • España Sandoz A tiempo completo

    At Sandoz, quality is a key factor embedded in our purpose of pioneering access for patients. As Manager Regulatory Affairs API in our Palafolls site, you'll provide timely preparation of high-quality CMC regulatory documentation for active ingredients/intermediates under your responsibility; formulate and lead global regulatory strategy for drug substances...


  • España ADM A tiempo completo

    Job Description At ADM, we’re dedicated to improving global health and wellness through cutting-edge ingredient solutions for both humans and animals. Our robust portfolio includes prebiotics, botanicals, plant-based oils, and microbiome solutions. We are seeking a Regulatory Affairs Manager to help drive compliance, open new markets, and ensure our...


  • España The Zonal Group A tiempo completo

    Job Details: Regulatory Affairs Specialist- EBDFull details of the job. Vacancy Name Vacancy Name Regulatory Affairs Specialist- EBD Vacancy No Vacancy No VN309 Employment Type Employment Type Full-Time Location About the JobSinclair is looking for a Regulatory Affairs Specialist to manage the global product...


  • España Archer Daniels Midland A tiempo completo

    Archer Daniels Midland – Valencia, ValenciaLegal, Compliance, Regulatory Affairs, Corporate SecurityJob DescriptionAt ADM, we’re dedicated to improving global health and wellness through cutting-edge ingredient solutions for both humans and animals. Our robust portfolio includes prebiotics, botanicals, plant-based oils, and microbiome solutions. We are...


  • España Michael Page ES A tiempo completo

    Reporting to the Regulatory Affairs Director, the Regulatory Affairs Specialist will be primarily responsible for:The preparation, submission, monitoring and updating of regulatory dossiers.Prepare high quality regulatory dossiers (novel food, enzymes, GRAS, etc.) needed for the marketing of our products or those of our business partners in different...


  • España AstraZeneca GmbH A tiempo completo

    Regulatory Affairs ManagerLocation: London St PancrasCompetitive salary, bonus & benefitsJoin our Biopharmaceuticals Business Unit as a Regulatory Affairs Manager and play a pivotal role in identifying regulatory strategies to support commercial and business objectives. This role offers the opportunity to plan and execute workload for defined product...


  • España Michael Page A tiempo completo

    Multinational Company | Career development opportunityMultinational company specialized in health supplements and bio ingredients.Reporting to the Regulatory Affairs Director, the Regulatory Affairs Specialist will be primarily responsible for:The preparation, submission, monitoring, and updating of regulatory dossiers.Preparing high-quality regulatory...


  • España Kenvue A tiempo completo

    Description Kenvue is currently recruiting for Regulatory Affairs intern Start Date : December 2024 Who we are At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including Neutrogena, Aveeno, Tylenol, Listerine, Johnson’s and BAND-AID® Brand...


  • España Grifols SA A tiempo completo

    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...


  • España Grifols A tiempo completo

    Senior 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...


  • España DSM Nutritional Products A tiempo completo

    Apprentice Regulatory Affairs Raw Materials TTHDSM Nutritional Products – Barcelona, BarcelonaRegulatory Affairs Raw Materials TTH ApprenticeBarcelona, SpainHybridC11Join our Raw Materials Team in Regulatory Affairs, where we use technology to turn regulatory information into meaningful data. This crucial role involves performing global compliance...

  • Energy Sourcing

    hace 2 días


    España Essity AB A tiempo completo

    Energy Sourcing & Regulatory Affairs Manager - SpainAbout the RoleThis position supports the strategy for energy procurement in Spain by sourcing energy for high-consumption sites within the framework of the global energy risk policy. You will manage regulatory issues related to energy consumption in Spain, ensuring compliance and competitiveness.We're...


  • España AbleCloset A tiempo completo

    Job Details: Senior Regulatory Affairs Engineer (Pre-Market)Full details of the job.Vacancy Name: Senior Regulatory Affairs Engineer (Pre-Market)Vacancy No: VN179Employment Type: Full-TimeLocation: Esplugues del Llobregat (Barcelona)The RoleSinclair is currently looking for a Pre-Market Regulatory Affairs Engineer at its offices located in Esplugues del...