Global Regulatory Lead: Medical Devices

Parexel is seeking an experienced Regulatory Affairs professional to lead regulatory strategy for medical devices and drug-device combinations across Europe. The role can be home or office based in various European locations.You will develop global regulatory strategies, interact with health authorities and notified bodies, and coordinate submissions while...

Parexel is seeking an experienced Regulatory Affairs professional to lead regulatory strategy for medical devices and drug-device combinations across Europe. Verifichi che le sue competenze e la sua esperienza corrispondano ai requisiti di questo ruolo, quindi si candidi con il suo CV qui sotto. The role can be home or office based in various European

Solventum is seeking a Territory Manager to drive sales of medical device solutions in the Operating Room and Intensive Care Unit for hospitals in the Campania region.Responsibilities include developing a sales plan, managing tenders, and maintaining relationships with key decision makers. The position requires a Bachelor's degree, at least 5 years of sales...

Hollister Incorporated is seeking a Sales Representative to drive growth in ostomy, continence, and critical care markets across a designated territory. The role emphasizes strategic selling, relationship building with distributors, hospitals, and clinicians, and achieving sales targets through education, contract management, and compliance with healthcare...

EVERSANA is seeking a Medical Information Content Developer to join our global Medical Information and Medical Content Development team. The role focuses on creating scientifically rigorous Medical Affairs materials, SRDs, FAQs, and training resources for clients, ensuring accuracy and alignment with MLR standards.The ideal candidate has a PhD or MSc in Life...

Tandem Health in Milan is hiring for a Global Medical Operations role. You will empower clinicians, scale Tandem’s AI OS, and roll out solutions to leading healthcare organizations worldwide.You’ll engage executives, medical leaders, and end-users to embed clinical insight into implementations. You will lead demos, design scalable workflows, and...

RISERVATO A CANDIDATI APPARTENENTI ALLE CATEGORIE PROTETTE - LEGGE 68/99 Lavorare presso QVC Group significa entrare a far parte di un’azienda di social shopping live con team incredibili, progetti ambiziosi e carriere straordinarie. QVC Group, Inc. è una società Fortune 500 con sei marchi leader nel settore retail – QVC®, HSN®, Ballard Designs®,...

Agilent Technologies in Italy is seeking a Lead Internal Auditor to plan, lead, and execute risk-based audits across regulated medical devices and pharmaceutical environments. You will act as a subject matter expert in quality systems and regulatory auditing, driving continuous improvement of the QMS within the Global Quality Organization.The role focuses on...

Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...