Die KI-Suchmaschine für Jobs
Senior Specialist, Global Regulatory Affairs(m/w/x)
Beschreibung
You will drive global compliance by managing product registrations and life cycle activities. Your day-to-day involves coordinating complex submissions and aligning regulatory strategies with portfolio goals.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •University degree in Veterinary Medicine
- •Multi-year regulatory experience in animal health
- •Excellent communication skills
- •Proficiency in English and MS Office
- •Proficiency with Veeva Vault
- •Result-oriented and well-structured working style
- •Strong interpersonal skills and sound judgement
- •Attentiveness to details
- •Experience in Drug Regulatory Affairs
- •Project Management skills
- •Ability to work across borders
Ausbildung
Berufserfahrung
ca. 4 - 6 Jahre
Aufgaben
- •Represent Global Regulatory Affairs in portfolio optimization projects
- •Implement new veterinary regulations and update packaging materials
- •Organize documents and data for marketing authorizations
- •Ensure materials align with the licensing strategy
- •Prepare technical statements with internal and external experts
- •Coordinate updates for product literature, leaflets, and labels
- •Manage regulatory submissions and respond to authority inquiries
- •Assess post-approval changes and provide filing strategies
- •Maintain regulatory information to ensure ongoing compliance
- •Develop technical knowledge of pharmaceutical product development
- •Communicate potential regulatory issues to management
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- •Flexible working hours
- •Hybrid working model
Sonstige Zulagen
- •13 monthly salaries
Boni & Prämien
- •Target bonus
Betriebliche Altersvorsorge
- •Attractive company pension scheme
Mehr Urlaubstage
- •30 days holiday entitlement
Weiterbildungsangebote
- •Internal training opportunities
- •Training on the job
Karriere- und Weiterentwicklung
- •Promotion opportunities
Sonstige Vorteile
- •International co-operations
- •Medicinal product development insights
- •Working across borders
Sinnstiftende Arbeit
- •Process design contribution
Parkplatz & Pendelvorteile
- •Free car parking
Großzügige Elternzeit
- •Paid Parental Time Off
- Merck & Co., Inc.Vollzeitmit HomeofficeSeniorSchwabenheim an der Selz
- Merck & Co., Inc.
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Senior Specialist, Global Regulatory Affairs(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
You will drive global compliance by managing product registrations and life cycle activities. Your day-to-day involves coordinating complex submissions and aligning regulatory strategies with portfolio goals.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •University degree in Veterinary Medicine
- •Multi-year regulatory experience in animal health
- •Excellent communication skills
- •Proficiency in English and MS Office
- •Proficiency with Veeva Vault
- •Result-oriented and well-structured working style
- •Strong interpersonal skills and sound judgement
- •Attentiveness to details
- •Experience in Drug Regulatory Affairs
- •Project Management skills
- •Ability to work across borders
Ausbildung
Berufserfahrung
ca. 4 - 6 Jahre
Aufgaben
- •Represent Global Regulatory Affairs in portfolio optimization projects
- •Implement new veterinary regulations and update packaging materials
- •Organize documents and data for marketing authorizations
- •Ensure materials align with the licensing strategy
- •Prepare technical statements with internal and external experts
- •Coordinate updates for product literature, leaflets, and labels
- •Manage regulatory submissions and respond to authority inquiries
- •Assess post-approval changes and provide filing strategies
- •Maintain regulatory information to ensure ongoing compliance
- •Develop technical knowledge of pharmaceutical product development
- •Communicate potential regulatory issues to management
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- •Flexible working hours
- •Hybrid working model
Sonstige Zulagen
- •13 monthly salaries
Boni & Prämien
- •Target bonus
Betriebliche Altersvorsorge
- •Attractive company pension scheme
Mehr Urlaubstage
- •30 days holiday entitlement
Weiterbildungsangebote
- •Internal training opportunities
- •Training on the job
Karriere- und Weiterentwicklung
- •Promotion opportunities
Sonstige Vorteile
- •International co-operations
- •Medicinal product development insights
- •Working across borders
Sinnstiftende Arbeit
- •Process design contribution
Parkplatz & Pendelvorteile
- •Free car parking
Großzügige Elternzeit
- •Paid Parental Time Off
Über das Unternehmen
3167 MSDAnimalHealthInnovation
Branche
Pharmaceuticals
Beschreibung
The company embraces the value of bringing diverse, talented, and committed people together to foster innovation in an inclusive environment.
- Merck & Co., Inc.
Senior Specialist Regulatory Affairs CMC(m/w/x)
Vollzeitmit HomeofficeSeniorSchwabenheim an der Selz - Merck & Co., Inc.
Senior Specialist Regulatory Affairs – CMC(m/w/x)
VollzeitBefristeter Vertragmit HomeofficeSeniorSchwabenheim an der Selz - SCHOTT Pharma AG & Co. KGaA
Expert Pharmaceutical Cleanroom Operations & Technology(m/w/x)
Vollzeitmit HomeofficeSeniorMainz - Ramboll
Regulatory Affairs Toxicologist REACH(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenMünchen, Bad Kreuznach, Frankfurt am Main, Berlin, Essen - Fusion Consulting
Senior Functional Consultant – Veeva Network Implementation(m/w/x)
Vollzeitmit HomeofficeSeniorMainz