Internship: Regulatory Affairs – English Speaking

Über das Unternehmen

Takeda is a global, values-based, R&D-driven biopharmaceutical leader headquartered in Japan, committed to discovering and delivering life-transforming treatments. We are focused on four therapeutic areas: Oncology, Rare Genetic and Hematology, Neuroscience, and Gastroenterology, with targeted investments in Plasma-Derived Therapies and Vaccines. Our mission is to strive for better health and a brighter future for people worldwide through leading innovation in medicine. With a presence in over 80 countries, Takeda fosters a diverse and inclusive environment where our employees are empowered to make a meaningful difference in patients‘ lives.

Stellenbeschreibung

Takeda is seeking a motivated and detail-oriented Intern for our Regulatory Affairs team in Josefstadt, Vienna. This is an excellent opportunity for an English-speaking student or recent graduate to gain hands-on experience in the pharmaceutical industry’s regulatory landscape. You will support critical activities that ensure our innovative medicines reach patients safely and efficiently.

As an intern, you will work closely with experienced regulatory professionals, contributing to various aspects of regulatory submissions and compliance. This role offers a unique chance to develop a strong foundation in regulatory processes within a global biopharmaceutical company. This position is an On-site, Full-Time Internship.

Hauptverantwortlichkeiten

• Assist in the preparation, compilation, and submission of regulatory documents to health authorities.
• Support the team in maintaining regulatory databases and tracking submission statuses.
• Conduct research on regulatory guidelines and requirements in various markets.
• Help with the review and archiving of regulatory correspondence and documentation.
• Participate in team meetings and contribute to discussions on regulatory strategies.
• Collaborate with cross-functional teams to gather necessary information for regulatory dossiers.

Erforderliche Fähigkeiten

• Excellent command of the English language (written and verbal).
• Strong attention to detail and accuracy.
• Ability to work effectively both independently and as part of a team.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
• Demonstrated interest in the pharmaceutical industry and regulatory affairs.
• Good organizational and time management skills.

Bevorzugte Qualifikationen

• Currently enrolled in or recently graduated from a degree program in Pharmacy, Life Sciences, Law, or a related field.
• Basic understanding of regulatory processes or a strong willingness to learn.
• Previous administrative or office experience is a plus.

Vorteile & Zusatzleistungen

• Hands-on experience in a leading global biopharmaceutical company.
• Mentorship from experienced regulatory professionals.
• Opportunities for professional development and networking.
• Contribution to meaningful work that impacts patient lives.
• Subsidized public transport ticket for Vienna.
• Access to Takeda's internal learning platforms.
• Modern office environment in a vibrant district.

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