Persönlich zum Erfolg beitragen als Quality Manager / Regulatory Affairs Manager (m/w/d) in Kempen Als mittelständisches Unternehmen im Bereich der Medizintechnik mit Hauptsitz in Planegg bei München feierten wir 2016

einen Umsatz von 12,8 Mrd. Euro (13,3 Mrd. US-Dollar) im Jahr 2021. Unser Team in Essen hat momentan eine freie Position als Manager Regulatory Affairs (m/w/d) zu besetzen. • Gefahrenanalysen HAZOP und Sicherheitsberichte

regulatory database. Our team provides product-specific data globally. • As substance coordinator, you are responsible for dedicated substances as main contact for questions related to Chemical Regulations within and outside BASF

: Minimum of a Bachelor university degree in the life sciences Graduate degree or certification in EU Regulatory Affairs is a definite asset Minimum 5 years of regulatory experience which included hands-on work in EU CTAs Hands-on

Job Title: Medical Affairs Manager Location: Remote (Germany) Rate: Competitive in line with skills / experience Type: Permanent My client, a rapidly expanding organisation currently seek a skilled Medical Affairs Manager

regulatory database. Our team provides product-specific data globally. • As substance coordinator, you are responsible for dedicated substances as main contact for questions related to Chemical Regulations within and outside BASF

regulatory database. Our team provides product-specific data globally. • As substance coordinator, you are responsible for dedicated substances as main contact for questions related to Chemical Regulations within and outside BASF

regulatory database. Our team provides product-specific data globally. • As substance coordinator, you are responsible for dedicated substances as main contact for questions related to Chemical Regulations within and outside BASF

regulatory database. Our team provides product-specific data globally. • As substance coordinator, you are responsible for dedicated substances as main contact for questions related to Chemical Regulations within and outside BASF

regulatory database. Our team provides product-specific data globally. • As substance coordinator, you are responsible for dedicated substances as main contact for questions related to Chemical Regulations within and outside BASF

regulatory database. Our team provides product-specific data globally. • As substance coordinator, you are responsible for dedicated substances as main contact for questions related to Chemical Regulations within and outside BASF

. Dir, Clinical Affairs and Programs, EMEA & APAC. This role entails training, managing, and developing CRAs and CTCs to ensure the controlled, compliant execution of clinical trials, prioritizing subject safety, privacy, and

Qualitätsmanagement (QM), Regulatory Affairs (RA), Forschung und Entwicklung (R&D) Ausarbeitung kundenspezifischer Lösungen zur Time-to-Market optimierten (agilen) Entwicklung, Prüfung und globalen Zulassung Vollumfängliche Verantwortung

Collaboration: Collaborate closely with cross-functional teams including Clinical Development, Regulatory Affairs, Medical Affairs, and Commercial to develop and implement strategic clinical development plans Vendor Management: Manage

: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications