GMP CQV Consultant – Life Sciences Onsite

ALTEN cerca profilo qualificato per condurre attività di Commissioning, Qualification e Validation in ambienti GMP, con presenza sul campo presso siti produttivi.La figura supporterà redazione di protocolli IQ, OQ e PQ, e la qualificazione di apparecchiature e sistemi critici utilizzati in produzioni sterili. Si richiede 2–3 anni di esperienza nelle...

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...

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...

pWould you like to start a new professional adventure as a bRegulatory Affairs Consultant /b in one of our opportunities in the bLife Sciences /b industry in bLatina (fully onsite position) ? /b /p ul liDraft and review Quality and CMC sections of regulatory dossiers, with a focus on Module 3 of the CTD. /li liPrepare and update pharmaceutical quality...

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...

pWould you like to start a new professional adventure as a bRegulatory Affairs Consultant /b in one of our opportunities in the bLife Sciences /b industry in bLatina (fully onsite position) ? /b /p ul liDraft and review Quality and CMC sections of regulatory dossiers, with a focus on Module 3 of the CTD. /li liPrepare and update pharmaceutical quality...

CAI Overview Are You Ready? CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For Life Sciences and Mission Critical industries that need to deliver critical solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled performance at the highest...

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...

CAI Overview Are You Ready? CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For Life Sciences and Mission Critical industries that need to deliver critical solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled performance at the highest...