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Rentschler Biopharma offers one-week internships for students in various fields, providing insights and experiences in their desired career areas with guidance from experienced mentors.

Rentschler Biopharma SE invites applicants for unlisted positions to contribute to biopharmaceutical production. The company values teamwork, offers flexible work arrangements, training, and benefits.

Lead and continuously develop the corporate website and digital experience, drive SEO and conversion optimization, manage CMS configurations and external agencies, coordinate content, campaigns and integrations with CRM/analytics, monitor KPIs and implement improvements to enhance digital discoverability and user engagement.

The Director of Business Development drives client acquisition for Rentschler's services in biopharmaceuticals, managing sales processes, territories, and cross-functional collaboration to achieve growth targets.

The program offers a dual study pathway in International Business, combining academic education with practical experience in a biopharmaceutical company.

This dual study program focuses on business informatics, combining IT concepts, programming, project management, and business management principles. Students will gain practical experience in a family-owned biotechnology company, with opportunities for personal development and career advancement.

The Quality Control Scientist will validate and qualify analytical methods for biologics in a GMP environment, ensuring compliance and executing analytical development activities.

The Director of Business Development is responsible for acquiring new clients, driving sales processes, and contributing to revenue growth in biotech and pharmaceutical sectors, while collaborating with cross-functional teams.

Rentschler Biopharma is offering positions for students seeking internships or theses. Candidates should express their area of interest and possible start dates.

The intern will assist with creating, controlling, and archiving equipment logbooks, support the development and revision of GMP documents, and aid in process optimizations and projects across departments.