Regulatory Affairs Specialist
Salva questo lavoro e mantieni la tua ricerca organizzata
Crea un account gratuito per salvare lavori, creare avvisi e tornare a questa inserzione dalla tua dashboard.
Continuando accetti i nostri Termini & Informativa sulla privacy.
Department: Regulatory, Quality & Compliance
€35,000–€50,000 gross annually
Role Overview
Chematek is seeking a Regulatory Affairs Specialist to support regulatory compliance activities for chemical substances and mixtures, ensuring conformity with European and UK chemical regulations.
Key Responsibilities
Prepare, review, and update Safety Data Sheets (SDS) and Exposure Scenarios (ES).
Review supplier SDS and verify regulatory compliance.
Manage REACH and UK REACH compliance activities.
Prepare and submit C&L Notifications, PCN notifications, and manage UFI codes.
Verify classification and labeling of substances and mixtures according to CLP.
Support product registration activities and regulatory submissions.
Maintain regulatory databases and compliance documentation.
Monitor regulatory developments and assess their impact on products and business activities.
Requirements
Degree in Chemistry, Industrial Chemistry, Chemical Engineering, Environmental Sciences, or related field.
Experience in Regulatory Affairs and SDS management.
Good knowledge of:
REACH and UK REACH
CLP Regulation
Safety Data Sheets (SDS)
UFI and PCN requirements
C&L Notifications
Chemical classification and labeling
Product registration processes
Fluent Italian and good English.
Strong attention to detail, organizational skills, and ability to work independently.
What We Offer
International working environment.
Direct involvement in European and global regulatory compliance activities.
Professional development and training opportunities.
Long-term career growth within a growing organization.
-
Regulatory Affairs Specialist
2 giorni fa
San Vittore Olona, Lombardia, Italia Chematek SpA Tempo pienoDepartment: Regulatory, Quality & Compliance €35,000–€50,000 gross annually Role Overview Chematek is seeking a Regulatory Affairs Specialist to support regulatory compliance activities for chemical substances and mixtures, ensuring conformity with European and UK chemical regulations. Key Responsibilities * Prepare, review, and update Safety Data...
-
Regulatory Affairs Specialist
4 giorni fa
Castiglione Olona, Lombardia, Italia ZEISS Group Tempo pienoCastiglione Olona, Varese (3 days on-site - 2 days smart working)Dato l'elevato interesse per questa posizione, la preghiamo di candidarsi tempestivamente se il suo profilo è in linea con il ruolo.Permanent, Full TimeZEISS is technology and innovation. Founded in Germany in 1846, we’re an internationally leading technology enterprise operating in the...
-
Regulatory Affairs Specialist
3 giorni fa
Ponte San Pietro, Lombardia, Italia Azienda Cliente Tempo pienoRicerca di uno Specialista Affari Regolatori per azienda produttrice di dispositivi medici a Brescia. La figura gestirà le autorizzazioni CE e US-FDA, la documentazione
-
Regulatory Affairs Specialist
1 giorno fa
San Vittore Olona, Lombardia, Italia Chematek SpA Tempo pienopChematek SpA in Lombardy, San Vittore Olona, seeks a Regulatory Affairs Specialist to support European and UK regulatory compliance for chemical substances and mixtures. You will help ensure conformity with REACH, CLP, SDS, UFI/PCN requirements, and manage registrations and documentation. /ppThe role offers an international environment, professional...
-
Regulatory Affairs Specialist
3 giorni fa
Ponte San Pietro, Lombardia, Italia A2A Tempo pienoRicerca di uno Specialista Affari Regolatori per la sede di Milano, da inserire nella struttura di regolazione del mercato elettrico, gas e idrogeno. La figura
-
Regulatory Affairs Specialist
2 giorni fa
San Vittore Olona (MI), Provincia di Milano; Lombardia, Italia Chematek SpA Tempo pienoChematek SpA in Lombardy, San Vittore Olona, seeks a Regulatory Affairs Specialist to support European and UK regulatory compliance for chemical substances and mixtures. You will help ensure conformity with REACH, CLP, SDS, UFI/PCN requirements, and manage registrations and documentation. The role offers an international environment, professional...
-
Regulatory Affairs Specialist
3 giorni fa
Induno Olona, Lombardia, Italia Azienda Tempo pienoSpecialista Affari Regolatori per mercati Extra-UE, responsabile della conformità dei prodotti (integratori, nutraceutici, dispositivi medici) e della gestione
-
Regulatory Affairs Specialist Senior
3 giorni fa
San Donato Milanese, Lombardia, Italia Iqmselezione Tempo pienoSpecialista Affari Regolatori con esperienza in ambito farmaceutico, gestirà le attività regolatorie per il mercato italiano, interfacciandosi con AIFA ed
-
Senior Regulatory Affairs Specialist For Pharma
3 giorni fa
San Donato Milanese, Lombardia, Italia Iqm Selezione Tempo pienoSocietà farmaceutica cerca un esperto Affari Regolatori a Milano con 5-10 anni di esperienza, laurea scientifica, per gestire attività regolatorie e preparare
-
Regulatory Affairs Specialist
6 giorni fa
Ponte San Pietro, Lombardia, Italia Hays Tempo pienoSpecialista Affari Regolatori per azienda farmaceutica. Responsabile della preparazione e aggiornamento della documentazione per la registrazione e il mantenimento