Regulatory Affairs Expert
6 godzin temu
At ManpowerGroup, we understand the importance of regulatory compliance in the pharmaceutical industry. As a global leader in workforce solutions, we provide cutting-edge recruitment and talent management services to help our clients succeed. Our commitment to excellence drives us to deliver top-notch professionals who can navigate complex regulatory landscapes with ease.
Job Description
We are seeking an experienced Regulatory Scientist to join our team. In this role, you will be responsible for providing crucial support to RSIL and RRL in navigating complex regulatory landscapes and optimizing product strategies. Your expertise will drive alignment between regional and global strategies by actively engaging in collaborative working groups and fostering strong relationships with regional stakeholders and LOCs.
Key Responsibilities:
- Develop and implement streamlined regulatory submission processes
- Lead the development of high-quality regulatory documents
- Collaborate with cross-functional teams to ensure seamless execution of regulatory requirements
- Provide expert guidance on CTA documents and clinical trial applications
- Support registration processes and maintain dossier readiness
Required Skills and Qualifications:
- Bachelor's Degree in Pharmacy, Chemistry, Medicine, or Biotechnology
- 2+ years of experience in regulatory affairs within the pharmaceutical industry
- Strong knowledge of regulatory submission requirements and compliance standards
- Proficiency in English (C1 level) and computer literacy
Benefits
As a valued member of our team, you will enjoy a stable job environment, international collaboration opportunities, and a comprehensive benefits package.
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