Onsite Regulatory Affairs Consultant — CTD Module 3 Expert

Amaris Consulting | Part of Mantu is seeking a Regulatory Affairs Consultant for a fully onsite position in Latina, Italy. You will draft and review CTD Module 3 quality sections, prepare documentation for new marketing authorisations and support clients through registrations and responses to deficiency letters.You should have a degree in a relevant...

Would you like to start a new professional adventure as a Regulatory Affairs Consultant in one of our opportunities in the Life Sciences industry in Latina (fully onsite position) ? 👉 Your missions? • Draft and review Quality and CMC sections of regulatory dossiers, with a focus on Module 3 of the CTD. • Prepare and update pharmaceutical quality...

Sei pronto ad entrare in una realtà internazionale che sta ridefinendo gli standard dell’industria farmaceutica e dei Medical Device? In PQE Group, la nostra divisione di Regulatory Affairs è sempre in una fase di grande crescita grazie ad un mercato in continua evoluzione che sempre più richiede la qualità dei nostri servizi. Per questo motivo abbiamo...

Would you like to start a new professional adventure as a Regulatory Affairs Consultant in one of our opportunities in the Life Sciences industry in Latina (fully onsite position) ? Draft and review Quality and CMC sections of regulatory dossiers, with a focus on Module 3 of the CTD. Prepare and update pharmaceutical quality documentation for new marketing...

Would you like to start a new professional adventure as a Regulatory Affairs Consultant in one of our opportunities in the Life Sciences industry in Latina (fully onsite position) ? Draft and review Quality and CMC sections of regulatory dossiers, with a focus on Module 3 of the CTD. Prepare and update pharmaceutical quality documentation for new marketing...

Amaris Consulting | Part of Mantu is seeking a Regulatory Affairs Consultant for a fully onsite position in Latina, Italy. You will draft and review CTD Module 3 quality sections, prepare documentation for new marketing authorisations and support clients through registrations and responses to deficiency letters.You should have a degree in a relevant...

Would you like to start a new professional adventure as a Regulatory Affairs Consultant in one of our opportunities in the Life Sciences industry in Latina (fully onsite position) ? Draft and review Quality and CMC sections of regulatory dossiers, with a focus on Module 3 of the CTD. Prepare and update pharmaceutical quality documentation for new marketing...