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Teva Intern - R&D Biologics CMC 
United States, Michigan 
170745938

26.01.2025

Embark on an experience with an international pharmaceuticals company, contributing your creative energy to high-impact projects from the moment you arrive through the course of this 12-week experience. You will take part in meaningful work and real-life projects that will help you grow both professionally and personally throughout the program.

How you’ll spend your day

• During the 12-week program, you will gain in-depth insight into the Biologics CMC department.
• Supported by a mentor and experienced colleagues, you will be directly involved in our daily business and be assigned tasks within diverse projects.
• You will also play an important role in the development of concepts and initiatives within the Material Sciences business unit.
• Use various coding software to develop a webpage that will contain current technical documents such as project specific Bill of Materials (BOMs), Materials Risk Assessments, impact memos, Regulatory Guidelines, and other critical documents that can be accessed across Teva’s Global Network.
• Create and develop an original centralized document management system for the Material Sciences organization that will be used as a repository for Extractables and Leachables data, BSE/TSE assessments, Nitrosamine and Melamine Statements.


Your experience and qualifications

• Currently enrolled in a Bachelor of Science program in Biology, Computer Science, Biotechnology, Data Science, Biochemistry, Chemistry or a related field of study.
• Fundamental understanding and experience in Microsoft Office Suite and related Software.
• Some experience in coding languages such as Python, Java Script, HTML or other coding software for webpage development, not mandatory.
• Experience managing large data files.
• Strong organizational skills and attention to detail.
• Excellent time management skills with ability to meet deadlines.
• Ability to function well in a high-paced environment, Self-starter.
• Some knowledge of the manufacturing processes, usage, and regulatory requirements associated with materials for pharmaceutical and biological products is not required, but beneficial.

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