Lavori attuali relativi a Quality Assurance R&D Pharmacovigilance Specialist - turbigo - Recordati
-
Pharmacovigilance Specialist
6 giorni fa
Turbigo, Italia Viatris A tempo pienoA global healthcare company is seeking a Pharmacovigilance Analyst in Turbigo, Italy. This role involves assisting in the review of pharmacovigilance SOPs, training team members, and performing local quality and compliance tasks. The ideal candidate should possess a Bachelor's degree in a scientific discipline, have at least three years of pharmacovigilance...
-
Pharmacovigilance Analyst
3 settimane fa
Turbigo, Italia Viatris Italia A tempo pienoA global healthcare company in Italy seeks a professional for a pharmacovigilance role. The candidate will be responsible for reviewing procedures, training teams, and ensuring compliance with legal standards. A minimum of 3 years of experience in pharmacovigilance and proficiency in both English and Italian are essential. This role offers competitive...
-
Quality Assurance Manager
3 settimane fa
Turbigo, Italia BTO Research A tempo pienoJoin to apply for the Quality Assurance Manager role at BTO Research
-
Quality Assurance Manager
1 settimana fa
turbigo, Italia BTO Research A tempo pienoJoin to apply for the Quality Assurance Manager role at BTO Research
-
Quality Assurance Manager
2 settimane fa
Turbigo (MI), Italia BTO Research A tempo pienoJoin to apply for the Quality Assurance Manager role at BTO Research Vuoi fare la differenza e lavorare dove il cambiamento si costruisce ogni giorno? Unisciti a noi! Chi è BTO? Siamo un centro di ricerca e consulenza indipendente del Gruppo Relatech, attivo in Italia e all'estero, dove affianchiamo organizzazioni e realtà complesse nei loro percorsi di...
-
Rif. 3768 – R&D SR SPECIALIST
2 settimane fa
Turbigo, Italia Arethusa A tempo pienoPer importante Azienda chimica, specializzata nella formulazione e produzione di soluzioni per la detergenza stiamo cercando un/una Senior R&D Specialist. Inserito/a all’interno del team Ricerca & Sviluppo e riportando alla Responsabile di Sviluppo Prodotto, la figura ricercata sarà il motore dell’innovazione formulativa. Non si occuperà solo di...
-
Quality Assurance GMP Assistant
2 settimane fa
Turbigo, Italia Fondazione Telethon A tempo pienoFondazione Telethon ETS is committed to developing therapeutic options for patients affected by rare genetic disorders. Fondazione Telethon pipeline consists in various programs at different development stages (from pre-clinical to commercial). For such programs, Fondazione Telethon is responsible, among others, for the production and distribution of...
-
Quality Assurance Manager
3 settimane fa
turbigo, Italia Generali Italia A tempo pienoThe role manages the overall testing strategy, tool selection, reporting, interfaces with providers and local contact, overseeing the activities of the quality assurance department and staff, developing, implementing, and maintaining a system of quality and reliability testing for the organization's products.Define, own, and implement the global Test...
-
Global Pharmacovigilance Support Specialist
3 settimane fa
Turbigo, Italia Viatris A tempo pienoA leading pharmaceutical company in Turbigo, Italy is seeking a Pharmacovigilance Support professional. The role involves managing inbound information and calls from healthcare professionals while liaising with relevant stakeholders to ensure data availability. Candidates should hold a Bachelor's degree in Scientific Disciplines and possess essential skills...
-
Project Quality Specialist
3 settimane fa
Turbigo, Italia Hitachi A tempo pienoAt Grid & Power Quality Solutions and Service businessat Hitachi Energy in Europe (HBUEU) Inclusiondrives our culture of innovation and collaboration. Our leading technology and strong market position enable us to achieve growth targets in the energy transition acrosscurrent and growing market segments such as hydrogen data centers and e-mobility.The Quality...
Quality Assurance R&D Pharmacovigilance Specialist
22 ore fa
OverviewWith its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro 2bn. We are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries. At Recordati, our mantra is simple. We’ve always believed that health, and the opportunity to live life to the fullest, is a right, not a privilege. Whether that is for common diseases or the rarest – we want to give people the opportunity to be the best version of themselves. This drive will never stop. Together, we will always be reimagining tomorrow – with new ideas, new technologies and new innovations to fight diseases. Recordati. Unlocking the full potential of life.Job PurposeThe primary objective of this function is to assure the development, implementation, and maintenance of Recordati's Quality Management System in relation to Pharmacovigilance, in alignment with Group and R&D quality standards. The role involves interaction with pharmacovigilance personnel at Headquarters, the PV contact person at each SPC Affiliate, and RRD PV personnel as required.The resource will coordinate the activities of Affiliates’ QA R&D for Pharmacovigilance and liaise with local QA teams. Additionally, the resource will manage the activities of its reporting personnel at RRD Sarl - Group QA R&D – PV RRD. The resource will report directly to the Group R&D – R&D QA Manager.ResponsibilitiesManagement of Quality Assurance activities to assure the compliance with Good Pharmacovigilance Practice and Pharmacovigilance applicable regulationManagement of SOPs/WIs on PV processesPharmacovigilance Audits managementQA Revision/approval of Deviations, CAPA, Change on PV topicsContribute of Training on GVP/Quality topicsContribute to Pharmacovigilance System Master File updates and reviewContribute to Quality Management system periodic reviewCollaborate to budget preparation and revision for PV activities and invoice verificationQuality oversight and support of the Pharmacovigilance teams with regard GVPCoordinate the activities of Local PV QAActive interaction and support within Group R&D QAPreparation of Group R&D SOPs/WIs on QA PV processesRevision of SOPs/WIs issued Recordati Departments/AffiliatesCollaborate with QA R&D Document Management and Affiliates QA for the revision and update of SOPs/WIs MatrixHQ PV system, Affiliates, Service Providers, Business Partners Audit managementManage/oversight /coordinate Affiliates’ PV auditsHQ and Affiliates Risk assessment management for audit prioritization (Affiliate, Partners, Service Providers, PV System)Strategic and Annual PV Audit Programme managementEnsure HQ and Affiliates inspection readinessRevision /approval of HQ and Affiliates Audit Plan/Report, Deviations, Audit/Inspection CAPA, Change controls on PV topicsRequired EducationLife science or other relevant qualificationsRequired Skills And Experience6-8 years experience in the same role in Pharmaceutical companies and/or PV CROsProject ManagementMicrosoft Word, Excel, PowerPoint, Teams and OutlookSoftware knowledge (e.g. eDMS)Computer System Validation knowledgeKnowledge of QA StandardsAbility to propose solutions, take decisions and/or refer to managerAbility to work across culturesFlexible and adaptableInitiatives and self-motivation capacitiesPositive thinking and enthusiasmAbility to travel on a periodic basisStrict on confidentiality, rules, procedures and timelinesPositive attitude and ability to interact and communicate diplomatically and professionally with internal and external customers in a global environmentExcellent organization skills and ability to handle multiple competing priorities within tight timelinesManagement / Leadership skillsRequired LanguagesFluent in English (spoken and written).At Recordati we believe in people Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential. We are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief. If you are looking to join a company where you can try new things, speak openly, and be bold, we invite you to apply today.#J-18808-Ljbffr
