Regulatory Affairs Manager (f/m/d) für Mannheim gesucht

Arbeits- und Stellenangebot im Regiobizz Arbeitsmarkt

Job Kategorie: Medizin/Pharma/Biotech Medizin/Pharma/Pflege

Stellenangebot Basisdaten

Arbeitsort:: DE 68161 Mannheim
Umkreis:: keine Angabe.
Art der Arbeitsstelle:
Letze Aktualisierung:: 14.11.20242024-11-14

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Stellenausschreibung: Regulatory Affairs Manager (f/m/d)

Arbeitgeber bzw. Arbeitsvermittler: GULP Information Services GmbH in Eschborn, Taunus

Branche: Medizin/Pharma/Biotech

Kategorie: Medizin/Pharma/Pflege

Stellenbeschreibung: Time for change – time for a new job! You are a regulatory affairs specialist and looking for a new professional challenge? Then stop searching! We offer the job you are looking for: Our subsidiary Randstad professional solutions offers a secure job, fair compensation and exciting new tasks at an attractive pharmaceutical company in Mannheim. Apply online now! We welcome applications from all suitably qualified persons regardless of any disabilities. Das dürfen Sie erwarten - Attractive salary and long-term job security through group affiliation - Up to 30 days vacation per year - Contribution to company pension scheme after end of probationary period - Extensive social benefits, including Christmas and vacation bonuses - Generally an open-ended employment contract - Good chances of being taken on by our business partner - Tailored further training opportunities and free language courses - 3 days/week remote-based work possible Ihre Aufgaben - Leading and supporting regulatory strategies for global product submissions - Ensuring compliance with international regulatory requirements and standards - Collaborating with cross-functional teams, including R&D, Quality and Clinical to drive regulatory initiatives - Providing regulatory guidance to support product development and lifecycle management - Staying abreast of evolving regulatory trends and updates, and implementing best practices Unsere Anforderungen - Bachelor’s degree in Life Sciences, Regulatory Affairs or a related field/alternatively completed vocational training with comparable experience in the regulatory field - Profound work experience in Regulatory Affairs; preferred in Regulatory, R&D, Quality, and/or Clinical, with some experience in Healthcare regulatory affairs - In-depth knowledge of global regulatory requirements, guidelines, and procedures especially for IVD instruments & medical devices - Affinity for IT and good MS Office skills - Fluent in English (for international meetings), German skills are not necessarily required - Strong organizational and communication skills - Ability to multitask and effectively manage multiple projects simultaneously - Self-motivated and capable of working independently in a self-management environment

Qualifikation: Arbeitskräfte

Verdienst:: 32767.00 - 32767.00 EUR

Bewerbung an: GULP Information Services GmbH
Frankfurter Straße 100
De 65760 Eschborn, Taunus
Telefon: +49 61 967548186
Email: alisa.tugai@randstad.de

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