Recherche Regulatory Diagnostics Senior Manager

Société: Novartis

Localisation: Bâle

Description de l’offre

Mandaté par une société établie en Suisse Romande, nous sommes à la recherche d’un / une Regulatory Diagnostics Senior Manager… Lire la suite

Job Description Summary #LI-Hybrid
Location: Basel, Switzerland
Relocation Support: This role is based in Basel, Switzerland. Novartis is unable to offer relocation support: please only apply if accessible.Are you ready to shape the future of regulatory precision medicine? As a Regulatory Diagnostics Senior Manager at Novartis, you’ll play a pivotal role in advancing our innovative medicines portfolio by driving regulatory strategies for in-vitro diagnostics, including companion diagnostics. Collaborating with cross-functional teams and global partners, you’ll ensure compliance and accelerate access to life-changing therapies. This is your opportunity to make a meaningful impact on global health while working at the forefront of in-vitro diagnostics innovation.Job DescriptionKey Responsibilities:– Design and implement regulatory strategies for precision in-vitro diagnostics and companion diagnostics globally– Lead submissions for investigational and pre-market in-vitro diagnostics in collaboration with regulatory therapeutics leads– Ensure integration of in-vitro diagnostics regulatory input into drug development strategies– Align with country regulatory teams to meet local requirements and deliver timely submissions– Prepare and coordinate briefing materials and participate in health authority meetings– Manage responses to health authority requests and oversee follow-up activities– Support compliance and training initiatives related to in-vitro diagnostics regulations and proceduresEssential Requirements:– Minimum 4–6 years of experience in the pharmaceutical industry with a focus on IVD/CDx– Proven track record contributing to regulatory projects involving in vitro diagnostics or companion diagnostics– Strong understanding of global regulatory pathways including IDE, NDA/BLA, 510(k), and PMA submissions– Familiarity with assay validation processes and Clinical Laboratory Improvement Amendments (CLIA) standardsWhy Novartis?Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?Benefits and rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:Accessibility & Accommodation : Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here:Skills Desired Clinical Trials, Cross-Functional Teams, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Problem Solving Skills, Regulatory Compliance, Risk Management Lire la suite

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✅ Recherche Regulatory Diagnostics Senior Manager
⚙️ Société: Novartis
🇨🇭 Lieu: Bâle

Identification de l’offre: A250–60PW-89

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Léa Harfi

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