摘要
About the Role
Your key responsibilities
• Provide scientific guidance and lead GMP-related analytical activities within the global project analytical sub-team for assigned projects in the clinical phase.
• Independently or under minimal supervision design, supervise and coordinate analytical activities, manage multiple tasks simultaneously, meet customer needs.
• Independently or under minimal supervision manage key tasks for release, stability studies, validation, transfer and implementation of analytical methods.
• Write analytical documentation, e.g. scientific protocols and reports intended for internal and external partners and support the preparation of registration documents.
• Contribute to budget and resource forecast, ensure cost awareness and manage project timelines.
• Actively drive knowledge sharing and present scientific results across organization and contribute to optimization of work processes.
• Ensure compliance of activities with quality standards (GMP), safety standards (HSE) and other Novartis standards.
Minimum requirements:
What you will bring to the role:
- University degree (preferable PhD) in pharmaceutical technology, biotechnology, biochemistry, chemical engineering or other relevant natural science discipline
- At least 3 years of working experience, preferably in pharmaceutical industry, biotechnology or other relevant industry.
- Excellent collaboration skills (ability to effectively work with others to achieve common goals through communication, teamwork, and problem solving).
- Quick learner, able to quickly grasp new concepts, passion for learning new things.
- Proficiency in oral and written English.
Desirable Requirements:
• Knowledge of Project management and GMP standards and regulations would be highly desirable.
• Strong proficiency in digital technologies would be an advantage.
We are looking for responsible, objective-driven candidates who value collaboration, teamwork and are open to new challenges and expanding their knowledge and expertise.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? http://www.novartis.com/about/strategy/people-and-culture
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: http://talentnetwork.novartis.com/network
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: http://www.novartis.com/careers/benefits-rewards
Adjustments for Applicants with Disabilities
If because of a medical condition, physical disability or a neurodiverse condition you require an adjustment during the recruitment process, please reach out to [email protected] and let us know the nature of your request as well as your contact information. The support which we can provide will include advice on suitable positions as well as guidance at all stages of the application process. Austrian law provides candidates the opportunity to involve the local disability representative, Behindertenvertrauensperson (BVP), in the application process. If you would like to request this, please let us know in advance as a note on your CV.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
