Lavoro Product Development Manager - Salerno

Adecco Italia SpA seleziona per azienda cliente operante nel settore chimico farmaceutico un Regulatory Affairs Specialist The Regulatory Affairs Specialist is responsible for establishing and sustaining CE Technical files, and final review of deliverables for MDR regulatory compliance. Furthermore,...

Job DescriptionThe Regulatory Affairs Specialist is responsible for establishing and sustaining CE Technical files, and final review of deliverables for MDR regulatory compliance. Furthermore, this position will be responsible for gathering and establishing documentation relevant to international re...

JOB DESCRIPTION - As a Territory Manager on our GENERAL SURGERY team, you will be able to offer your customers a full range of products and solutions with a high technological profile. ConMed is committed to providing differentiated products that help physicians achieve superior outcomes for their p...

Description Product Specialist, GI - Campania About Astellas At Astellas we can offer an inspiring place to work and a chance to make your mark in doing good for others. Our expertise, science and technology make us a pharma company. Our open and progressive culture is what makes us Astellas. It’s a...

About AbboAbbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.PURPO...

Job Description:The Regulatory Affairs Specialist is responsible for establishing and sustaining CE Technical files, and final review of deliverables for MDR regulatory compliance. Furthermore, this position will be responsible for gathering and establishing documentation relevant to international r...

Adecco Italia SpA seleziona per azienda cliente operante nel settore chimico farmaceutico un Regulatory Affairs SpecialistThe Regulatory Affairs Specialist is responsible for establishing and sustaining CE Technical files, and final review of deliverables for MDR regulatory compliance. Furthermore, ...