Aktuelle Jobs im Zusammenhang mit Regulatory Affairs Support Intern - Zug - Opella
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Regulatory Affairs Manager
vor 2 Wochen
Zug, Schweiz Johnson & Johnson VollzeitJohnson & Johnson is currently seeking a Regulatory Affairs Manager to join our local Regulatory Affairs team located in Zug, Switzerland. This role will be working in a hybrid working model. We are looking for a highly motivated individual to join our team as a Regulatory Affairs Manager. In this position, you will play a crucial role in ensuring adherence...
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Executive Director, Regulatory Affairs
vor 19 Stunden
Zug, Schweiz Mirati Therapeutics Inc Vollzeit**Job Description Summary** Reporting to the SVP and Head of International, based in Zug, and the VP Regulatory Affairs & Quality, based in San Diego, this professional will be part of both the International Leadership and the Global Regulatory Affairs Teams with responsibility for oversight of EU and International Regulatory activities to support corporate...
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Senior Expert Regulatory Affairs
vor 1 Tag
Zug, Zug, Schweiz gloor&lang AG VollzeitShape CMC regulatory strategy for complex biologics in a fast-growing biotech environmentFor a fast-growing, internationally active biotech company focused on biosimilar development, we are currently looking for a Senior Expert Regulatory Affairs with a strong CMC focus. Workplace is Region Zug-Zurich in Switzerland, 3d office required.This is a key role...
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Senior Expert Regulatory Affairs
vor 1 Tag
Zug, Zug, Schweiz gloor&lang AG VollzeitShape CMC regulatory strategy for complex biologics in a fast-growing biotech environmentFor a fast-growing, internationally active biotech company focused on biosimilar development, we are currently looking for a Senior Expert Regulatory Affairs with a strong CMC focus. Workplace is Region Zug-Zurich in Switzerland, 3d office required.This is a key role...
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Senior Expert Regulatory Affairs
vor 3 Wochen
Zug, Schweiz gloor&lang AG VollzeitShape CMC regulatory strategy for complex biologics in a fast-growing biotech environment For a fast-growing, internationally active biotech company focused on biosimilar development, we are currently looking for a Senior Expert Regulatory Affairs with a strong CMC focus. Workplace is Region Zug-Zurich in Switzerland, 3d office required. This is a key role...
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Intern Regulatory Affairs
Vor 3 Tagen
Zug, Schweiz Viatris VollzeitViatris Pharma GmbH At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via: Access - Providing high quality trusted medicines regardless of...
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Senior Expert Regulatory Affairs
vor 3 Wochen
Zug, Schweiz gloor&lang AG VollzeitShape CMC regulatory strategy for complex biologics in a fast-growing biotech environment For a fast-growing, internationally active biotech company focused on biosimilar development, we are currently looking for a Senior Expert Regulatory Affairs with a strong CMC focus. Workplace is Region Zug-Zurich in Switzerland, 3d office required.This is a key role...
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Senior Expert Regulatory Affairs
Vor 2 Tagen
Zug, Schweiz gloor&lang AG VollzeitShape CMC regulatory strategy for complex biologics in a fast-growing biotech environment For a fast-growing, internationally active biotech company focused on biosimilar development, we are currently looking for a Senior Expert Regulatory Affairs with a strong CMC focus. Workplace is Region Zug-Zurich in Switzerland, 3d office required. This is a key role...
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Global Regulatory Affairs Manager, Vaccines
vor 2 Wochen
Zug, Schweiz GSK Vollzeit**Site Name**: Belgium-Wavre, Italy - Siena, Switzerland - Zug, UK - London - New Oxford Street, USA - Maryland - Rockville, Warsaw Rzymowskiego 53 **Posted Date**: Oct 31 2024 **Global Regulatory Affairs Manager, Vaccines Therapeutic Group**: Job purpose: As a **Global Regulatory Affairs (GRA) Manager**, you will join the GRA Vaccines Therapeutic Group in...
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Drug Regulatory Affairs Manager
vor 1 Woche
Zug, Schweiz nemensis ag VollzeitAt nemensis ag, we have connected thousands of applicants with their dream job and given them the opportunity to develop or re-enter the job market. For our client, an international pharmaceutical company in Rotkreuz, we are looking for a Drug Regulatory Affairs Manager. **Job Purpose**: Takes care of all drug regulatory affairs matters regarding the...
Regulatory Affairs Support Intern
vor 2 Wochen
Opella is the self-care challenger with the purest and third-largest portfolio in the Over-The-Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market globally.Our mission: to bring health in people's hands by making self-care as simple as it should be for over half a billion consumers worldwide.At the core of this mission is our 100+ loved brands, our 11,000-strong global team, our 13 best-in-class manufacturing sites and four specialized science and innovation development centers.Headquartered in France, Opella is the proud maker of many of the world's most loved brands, including Allegra, Buscopan, Doliprane, Dulcolax, Enterogermina, Essentiale and Mucosolvan.B Corp certified in multiple markets, we are active players in the journey towards healthier people and planet.Find out more about our mission to bring health in your hands at About The JobWe are looking for a student (all genders) for a 1-year contract, full-time (40h/week) to support the Regulatory Affairs team in Switzerland. The position is opened in Rotkreuz (Zug). The student will support in the submission and follow up of regulatory dossiers to Health Authority (variations and new registrations) and transversal activities (promotional material review, artwork process, database update...).Main ResponsibilitiesSupport for the Regulatory lifecycle management of existing portfolio in Switzerland (medicinal products (Rx and OTC) and medical devices)Contribution to labelling and CMC variationsContribution to Innovation projects (new registration, line extension...)Participation in and coordination of transversal regulatory projectsReview of promotional materialsSupport for the update and review of artworksOrganization of administrative documents (PoA, CPP, etc.)Regulatory database maintenanceAbout YouExperience: First experiences in working in a pharma or medical device company would be an advantage.Skills: Proficiency in MS Office package and interest in working with database systems, accurate and precise working attitude, strong time management and prioritization skills, Team player and good communication as well as project management and organizational skills.Education: University degree in pharmacy or other life science discipline such as Biology, Medicine, Chemistry, etc. is preferred. Knowledge in Regulatory Affairs and Swissmedic regulations would be an advantage.Languages: Fluent in German and English (French or Italian in addition would be an asset).Why us?At Opella, you will enjoy doing challenging, purposeful work, empowered to develop consumer brands with passion and creativity. This is your chance to grow new skills and be part of a bold, collaborative, and inclusive culture where people can thrive and be at their best every day.We Are Challengers.We Are Dedicated To Making Self-care As Simple As It Should Be. That Starts With Our Culture. We Are Challengers By Nature, And This Is How We Do ThingsAll In Together:We keep each other honest and have each other's backs.Courageous:We break boundaries and take thoughtful risks with creativity.Outcome-Obsessed:We are personally accountable, driving sustainable impact and results with integrity.Radically Simple:We strive to make things simple for us and simple for consumers, as it should be.Join us on our mission. Health. In your hands.
