About this role
Randstad is one of the world's leading talent companies with the ambition to be the world's most equitable and specialized talent company. Through our "partner for talent" corporate strategy, we find, develop and connect specialized talents with companies - worldwide, locally and always at a high speed. We build high-quality, diverse, and agile teams, while individuals can enjoy a rewarding career path with equitable opportunities. Randstad Professional is one of Randstad's four specializations and focuses on the placement of specialists and managers in the future-oriented sectors of IT, Engineering, Life Science and Office. Are you an experienced regulatory professional looking to advance your career with an industry leader in Penzberg's thriving healthcare sector? Join an innovative team where you will independently drive complex global registration projects and help deliver groundbreaking solutions to patients worldwide. If you excel in an agile environment and thrive at the intersection of science and global compliance, we would love to welcome you aboard. - Dossier & Submission Management: Lead the preparation and execution of complex regulatory submission dossiers for global markets while mentoring junior team members. - Strategy & Compliance: Formulate region-specific regulatory strategies, anticipate compliance hurdles, and mitigate risks to accelerate market entry. - Cross-Functional Stakeholder Engagement: Partner with key internal and external stakeholders—including R&D, QC, and international regulatory bodies—to drive alignment and support audits. - Agile Leadership & Innovation: Champion continuous improvement, adopt digital regulatory tools, and influence cross-functional project teams to foster an inclusive, solution-oriented culture. - Problem Solving & Decision Making: Independently resolve complex compliance issues, leverage data stewardship, and drive process optimization across all regulatory operations. - Degree in Life Sciences, Data Science, or equivalent technical qualification combined with relevant hands-on experience. - At least 5 to 7 years of experience in Regulatory Affairs, R&D, Quality, Operations, or Clinical environment. - Proven track record of independently managing complex global projects with minimal supervision. - Fluent in spoken and written English with excellent communication and conflict-resolution skills. - Experience with Chinese regulatory affairs is strongly preferred. - Attractive salary and long-term job security through affiliation with the Group - 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