Microbiologist (m/f/d) - Regulatory Affairs

Ramboll; Bad Kreuznach; Vor Ort; EUR 50.000 - 80.000; Vollzeit

Zusammenfassung

Ein etabliertes Unternehmen sucht einen Mikrobiologen für die Abteilung Regulatory Affairs. In dieser spannenden Rolle werden Sie Teil eines dynamischen Teams, das sich mit der Bewertung und Genehmigung von Biociden beschäftigt. Ihre Hauptaufgabe besteht darin, die Wirksamkeit von Produkten zu bewerten und Genehmigungsdossiers zu erstellen. Sie profitieren von flexiblen Arbeitszeiten, intensiver Einarbeitung und einem unterstützenden Arbeitsumfeld. Wenn Sie eine Leidenschaft für Naturwissenschaften haben und in einem interdisziplinären Team arbeiten möchten, ist dies die ideale Gelegenheit für Sie.

Leistungen

Flexible Arbeitszeiten

Job Bike

Intensive Einarbeitung

Betriebliche Altersvorsorge

Essenszulage

Teamevents

Qualifikationen

• 5-7 Jahre Erfahrung in der Wirksamkeit von Biociden und deren Regulierung.
• Fähigkeit, komplexe Probleme effektiv zu koordinieren.

Aufgaben

• Bewertung der Wirksamkeit von Biociden und Management von Registrierungsprojekten.
• Vorbereitung von Dossiers für biocide Produkte in Europa.

Kenntnisse

Efficacy assessment

Project management

Regulatory compliance

Strong communication skills

Organizational skills

Ausbildung

Science degree in natural sciences

Tools

IUCLID

R4BP3

SPC

Jobbeschreibung

Microbiologist (m/f/d) - Regulatory Affairs

Employer: Ramboll
Location: Bad Kreuznach, Rheinland-Pfalz, Germany
Salary: Competitive
Closing date: 6 Apr 2025

Company Description
Welcome to SCC, part of the Ramboll Group, one of Europe's biggest consultancy companies in the regulation sphere, and a respected partner of the chemical and pharmaceutical industry. Our passion: managing registration and approval procedures for agrochemicals and biorationals, chemicals, biocides as well as pharmaceuticals and medical devices.

Job Description
Expand our scientific expertise as Microbiologist (m/f/d) - Regulatory Affairs

WHAT YOU CAN EXPECT

• Your path is taking you into a team of currently 28 people - and right into our enormous diversity of projects.
• Your tasks: assessment of efficacy of various substances and products mainly in the field of biocides and managing projects in the field of registration under the BPR and other biocidal regulations.
• Your mission: in collaboration with your colleagues, you will prepare biocidal active substance or product dossiers, plan and coordinate studies and engage in various regulatory projects.
• Your focus: to obtain approvals/authorizations for our client's active substances/biocidal products in the European market.

WHAT YOU OFFER

• Science degree in natural sciences (microbiology or related scientific disciplines).
• Preferably at least 5-7 years' experience in efficacy of biocide actives and/or products and in dealing with the BPR and other regulation of biocides.
• Ability to tackle and coordinate complex issues effectively.
• A talent for organisation, goal orientation and awareness of deadlines.
• Experience with regulatory software tools such as IUCLID, R4BP3 and SPC is of advantage.
• Strong communication and presentation skills in German and English.

WHAT WE OFFER

• Flexible working hours as well as the possibility of mobile working.
• Job Bike.
• Intensive on-the-job training and opportunities for personal and professional development.
• An appreciative working environment.
• An attractive salary with profit-sharing, bonuses and benefits (company pension plan, food allowance, etc.).
• A very good working atmosphere in a team supported by corporate events and socialising outside of work.

Do you thrive on challenging projects in an interdisciplinary team of ambitious professionals? Then apply online via the link below!

For any questions on job specifics, please contact Dr Henry von Rège (Team Lead Efficacy), Tel: [phone], [e-mail]

For questions relating to the application process, please contact our HR-Team, Tel: [phone], [e-mail]