A medical device company in Genova is seeking a Senior Clinical Research Associate responsible for monitoring clinical trials and ensuring data accuracy. This role requires a minimum of 5 years' experience in clinical monitoring and strong organizational skills. The ideal candidate will also conduct training sessions and ensure compliance with regulatory standards. The position offers opportunity...
What to Expect Conduct regulatory impact assessments for product changes, including determination of letter-to-file versus submission requirements. Manage annual registrations, license renewals, and ongoing regulatory notifications. Support the preparation, submission, and maintenance of FDA dossiers and related technical documentation. Coordinate the collection, review, and consolidation of data...
COMPANY Our client is a fast-growing and innovative startup operating at the intersection of plastics and medical technology. Backed by international investors, they are developing advanced solutions in the medical device space, particularly around injectable systems. With a strong foundation in mechanical engineering, team is working on cutting-edge pharmaceutical delivery systems that have the...
COMPANY Our client is a fast-growing and innovative startup operating at the intersection of plastics and medical technology. Backed by international investors, they are developing advanced solutions in the medical device space, particularly around injectable systems. With a strong foundation in mechanical engineering, their team is working on cutting-edge pharmaceutical delivery systems that...
A leading manufacturer of medical devices is seeking a Temporary Project Manager for regulatory compliance. The ideal candidate should have solid project management training, experience in medical device regulations, and strong communication skills in Italian and English. This role involves coordinating multidisciplinary teams and executing compliance action plans in a high-pressure environment,...
A global leader in medical technologies is seeking a Territory Manager in Italy. This role involves supervising sales, optimizing customer service, and managing a sales team. Candidates should have over 6 years of medical device sales experience, fluency in Italian (C2) and intermediate English (B2). The position requires significant travel (70%) and offers competitive salary and benefits. Join a...
A leading medical technology company in Italy is seeking a Field Service Engineer responsible for repairing and maintaining Stryker medical devices. This role requires technical expertise and customer interaction, ensuring compliance with specifications and quality standards. Ideal candidates will have a Bachelor's degree in engineering, experience in medical device repair, and fluency in Italian...
Entrare in PQE Group significa mettere la propria esperienza al centro di progetti strategici per i leader globali del settore Life Sciences. Dal **** PQE Group è un punto di riferimento internazionale nella consulenza per l'industria farmaceutica e deiMedical Device. Con una presenza consolidata in Europa, Asia e Americhe, 45 filiali e oltre ***** professionisti, supportiamo i principali player...
Territory Sales Manager – Inserta Italia (Veneto) Vendite sul campo | Nuovo business | Ruolo ad alta responsabilità In tutta Europa, Inserta sta trasformando l'implantologia grazie a tecnologie brevettate, a un ecosistema digitale avanzato e a uno dei flussi di lavoro full-arch più efficienti del mercato. Le nostre soluzioni aiutano i clinici a lavorare con maggiore precisione, efficienza e...
Work Flexibility: Field-based As Field Service Engineer you will be responsible for the repair and preventative maintenance of Stryker products in the Medical division, ensuring compliance with the quality system and manufacturer specifications. You will provide technical support and documentation to internal and external customers. Please apply with your CV in English. Geographical area:...
Biopharmed è la boutique di head hunting progettata per la ricerca e selezione di profili tecnici e specialistici del mondo Life Sciences & Chemical . Posizione Ricerchiamo una figura da inserire nel team Regulatory Affairs for Medical Devices per importante azienda operante nel settore farmaceutico e del medical device. Principali Responsabilità Coordinamento del team Regulatory Affairs per...
A leading medical device company in Bussolengo seeks a Junior Embedded Electronics Engineer to join their R&D team. The role requires expertise in electronics circuit design and programming in C/C++. Responsibilities include prototype development, product testing, and ensuring compliance with medical device regulations. The ideal candidate will have a master's degree and experience in a regulated...
Entrare in PQE Group significa mettere la propria esperienza al centro di progetti strategici per i leader globali del settore Life Sciences. Dal **** PQE Group è un punto di riferimento internazionale nella consulenza per l'industria farmaceutica e dei Medical Device . Con una presenza consolidata in Europa, Asia e Americhe, 45 filiali e oltre ***** professionisti, supportiamo i principali...
A leading medical device firm in Liguria seeks an experienced Temporary Project Manager to lead regulatory compliance initiatives for EU Class II and III medical devices. The successful candidate will be responsible for coordinating multidisciplinary teams, ensuring compliance with international regulations, and managing project timelines. Strong training in project management methodologies and...
As Field Service Engineer you will be responsible for the repair and preventative maintenance of Stryker products in the Medical division, ensuring compliance with the quality system and manufacturer specifications. You will provide technical support and documentation to internal and external customers. Please apply with your CV in English. Geographical area: Tuscany, Lazio and...
Mission Overview We are seeking an experienced Temporary Project Manager to lead, on a day-to-day basis, the definition, execution, and monitoring of a comprehensive regulatory compliance action plan for EU Class II and Class III medical device technical documentation. Operating in a high-pressure and time-critical environment, the Project Manager will play a pivotal role in ensuring full...
Mission OverviewWe are seeking an experienced Temporary Project Manager to lead, on a day-to-day basis, the definition, execution, and monitoring of a comprehensive regulatory compliance action plan for EU Class II and Class III medical device technical documentation.Operating in a high-pressure and time-critical environment, the Project Manager will play a pivotal role in ensuring full alignment...
A leading manufacturer of medical devices is seeking a Temporary Project Manager for regulatory compliance. The ideal candidate should have solid project management training, experience in medical device regulations, and strong communication skills in Italian and English. This role involves coordinating multidisciplinary teams and executing compliance action plans in a high-pressure environment,...
A leading medical device firm in Liguria seeks an experienced Temporary Project Manager to lead regulatory compliance initiatives for EU Class II and III medical devices. The successful candidate will be responsible for coordinating multidisciplinary teams, ensuring compliance with international regulations, and managing project timelines. Strong training in project management methodologies and...
A leading manufacturer of medical devices is seeking a Temporary Project Manager for regulatory compliance. The ideal candidate should have solid project management training, experience in medical device regulations, and strong communication skills in Italian and English. This role involves coordinating multidisciplinary teams and executing compliance action plans in a high-pressure environment,...