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- Aufgaben: Guide clients through complex pharmaceutical regulations in Germany and Switzerland.
- Arbeitgeber: Join a dynamic team focused on regulatory affairs in the EU.
- Mitarbeitervorteile: Enjoy flexible work options, whether from home or the office.
- Warum dieser Job: Make an impact in the pharmaceutical industry while collaborating with diverse teams.
- Gewünschte Qualifikationen: Fluent in German and English with experience in regulatory affairs required.
- Andere Informationen: Work on exciting projects and contribute to innovative product applications.
Das voraussichtliche Gehalt liegt zwischen 48000 - 84000 € pro Jahr.
Are you a fluent German speaker with expertise in regulatory affairs? Do you have a passion for navigating the complex world of pharmaceutical regulations in Germany, Switzerland, and the EU? We are seeking a talented and experienced Regulatory Affairs Consultant to join our dynamic team!
The role can be home or office based in various European locations.
Key Responsibilities:
- Provide strategic guidance on regulatory requirements and submissions in Germany and Switzerland
- Support national dossier filings and contribute to centralized dossier preparation
- Offer expert advice on new product applications and lifecycle maintenance
- Lead small-scale projects or work streams, ensuring client satisfaction and project success
- Collaborate with cross-functional teams to deliver high-quality regulatory solutions
Ideal Candidate Profile:
- University degree in a scientific area
- Several years of experience in regulatory affairs, specifically in German and Swiss markets
- Experience working with Swissmedic and BfArM
- In-depth knowledge of international regulatory requirements
- Strong understanding of EU regulatory landscape
- Excellent project management and client communication skills
- Ability to work independently and as part of a team
- Proactive problem-solver with keen attention to detail
- Fluent English and German speaker (required)
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Regulatory Affairs Consultant - Switzerland & Germany Arbeitgeber: Parexel
Kontaktperson:
Parexel HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Regulatory Affairs Consultant - Switzerland & Germany
✨Tip Number 1
Make sure to network with professionals in the regulatory affairs field, especially those who have experience with Swissmedic and BfArM. Attend industry conferences or webinars where you can meet potential colleagues and learn more about the latest trends in pharmaceutical regulations.
✨Tip Number 2
Familiarize yourself with the specific regulatory requirements for both Germany and Switzerland. This knowledge will not only help you in interviews but also demonstrate your commitment to understanding the nuances of the markets.
✨Tip Number 3
Prepare to discuss your previous experiences in regulatory affairs during the interview. Highlight any successful projects you've led or contributed to, especially those that involved cross-functional collaboration.
✨Tip Number 4
Showcase your language skills by being fluent in both German and English. If possible, practice discussing regulatory topics in both languages to ensure you're comfortable communicating complex information clearly.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Regulatory Affairs Consultant - Switzerland & Germany
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description and understand the key responsibilities and ideal candidate profile. Tailor your application to highlight your relevant experience in regulatory affairs, especially in the German and Swiss markets.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience with Swissmedic and BfArM, as well as any specific projects you've managed that relate to regulatory submissions in Germany and Switzerland.
Showcase Language Skills: Since fluency in German and English is required, make sure to clearly state your language proficiency in your application. If you have any certifications or relevant experiences that demonstrate your language skills, include those.
Personalize Your Cover Letter: Write a compelling cover letter that not only outlines your qualifications but also expresses your passion for regulatory affairs and your interest in the company. Mention how your proactive problem-solving skills can contribute to their team.
Wie du dich auf ein Vorstellungsgespräch bei Parexel vorbereitest
✨Showcase Your Regulatory Knowledge
Be prepared to discuss your experience with Swissmedic and BfArM. Highlight specific projects where you navigated regulatory requirements successfully, demonstrating your expertise in the German and Swiss markets.
✨Demonstrate Project Management Skills
Since the role involves leading small-scale projects, share examples of how you've managed projects in the past. Discuss your approach to ensuring client satisfaction and delivering high-quality results.
✨Emphasize Communication Abilities
Effective communication is key in regulatory affairs. Be ready to explain how you collaborate with cross-functional teams and maintain clear communication with clients. Provide examples of successful interactions.
✨Prepare for Language Proficiency Questions
As a fluent German and English speaker, be prepared to demonstrate your language skills during the interview. You might be asked to discuss complex regulatory topics in both languages, so practice articulating your thoughts clearly.
