Jobs für fda bei Genf

Location: Geneva, Switzerland (Minimum 4 days office presence per week) Travel Requirements: 20-30% (Includes site visits to European, US, and Asian manufacturing partners) Reporting To: Head of Industrial Affairs Position Summary We are seeking a highly skilled Drug Product Outsourcing Lead to serve as the primary point of contact for our Contract...

Drive compliance for innovative healthcare products. Grow in a collaborative, cross-functional R&D environment. About Our Client Our client is a global leader in the life sciences and bioprocessing industry, delivering innovative technologies. Operating in a highly regulated environment, the company is committed to quality, compliance, and continuous...

Select how often (in days) to receive an alert:At Sonova, we envision a world where everyone can enjoy the delight of hearing. This vision inspires us and fuels our commitment to developing innovative solutions that improve hearing health and human connection - from personal audio devices and wireless communication systems to hearing aids and cochlear...

DNDi and Medicines for Malaria Venture (MMV) have joined forces to create a shared Regulatory Sciences Platform. We seek a senior, strategic Regulatory Sciences Manager with global experience to lead regulatory strategy across development, registration, lifecycle management and access.The role interfaces with EMA, FDA, Swissmedic, WHO and regulators in...

A leading pharmaceutical company in Switzerland is seeking a highly skilled professional for their R&D department. The role involves developing and characterizing prototype formulations for small molecules and conducting analytical assessments. Candidates need a Master's degree in a relevant science field and a minimum of ten years' experience in the...

## QA Operations SpecialistApplylocations: CHE - Plan-les-Ouatestime type: Full timeposted on: Posted Yesterdaytime left to apply: End Date: September 1, 2026 (30+ days left to apply)job requisition id: JR100215**Contract type:**PermanentBracco is an international Group active in the healthcare sector and a leader in diagnostic imaging. The...

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait. We started in 1984 with a modest investment, 20 employees and a...

How You'll Make An ImpactProvide technical consulting services that leverage Ecolab’s expertise in chromatography resin performance, downstream purification, and regulatory change management to help commercial teams understand customer needs and increase account revenue.Act as a pre-sales and customer-facing technical expert for Biopharma opportunities,...

DNDi and MMV are seeking a Senior Regulatory Sciences Manager to lead regulatory strategies for a joint platform spanning early development to access. The role is embedded across DNDi and MMV, reporting to the Directors of Regulatory Sciences, with interactions across EMA, FDA, Swissmedic and WHO, and a focus on patient access in LMICs.The candidate will...

Fortil, groupe international d’ingénierie, recherche un ingénieur senior CQV pour renforcer son activité en Suisse (Genève). Vous piloterez la stratégie CQV des projets conformes GMP/FDA/EMA, tout en assurant l’interlocution client et le pilotage technique.Vous superviserez la documentation de qualification (VP, IQ/OQ/PQ, DQ, RAP) et les campagnes...

Groupe international d’ingénierie et d’expertise en technologies, fortil repose sur un modèle indépendant et rassemble plus de 2 500 collaborateurs. Avec 30 agences réparties dans 14 pays, fortil cultive la liberté d’entreprendre et la libération des potentiels. Description Du Poste Dans le cadre du développement de nos activités en Suisse,...

Drive compliance for innovative healthcare products. Grow in a collaborative, cross-functional R&D environment. About Our ClientOur client is a global leader in the life sciences and bioprocessing industry, delivering innovative technologies. Operating in a highly regulated environment, the company is committed to quality, compliance, and...

JUNIOR REGULATORY AFFAIRS & QUALITY SPECIALIST Help bring innovative medical technology to patients around the world. Join Medimaps Group and become part of our growing Regulatory Affairs & Quality team, supporting the compliance and quality of innovative AI-powered medical imaging software used internationally. This is an excellent opportunity...

Anteris® Technologies is a global structural heart company dedicated to revolutionizing cardiac care. With offices in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia, we have a growing and inclusive team. Our mission is to forge new frontiers in cardiac care by pioneering science-driven and measurable advancements...