Sommario
About the Role
Major accountabilities:
- Oversee and lead all activities of assigned teams /projects; meet customer needs.
- Work according to appropriate standards for quality, ethics, health, safety, environment, protection and information security; lead initiatives to ensure continuous improvement; all activities have to be aligned with organizational workflows and procedures.
- Evaluate and interpret results, draw relevant conclusions; supervise project related activities; perform complex tasks without having established procedures.
- Oversee and also write protocols, scientific reports, lab procedures or process, related SOPs; write scientific documents intended for external partners or for generation of registration documents; interact with authorities.
- Communicate, address and solve problems within own and broader area of responsibility; communicate effectively across organizational interfaces; lead the transfer of know how to other departments or external contractors, including troubleshooting and on site training.
- Develop analytical control strategies and collaborate with formulation development team to provide analytical solutions to complex challenges; lead the optimization of project related scientific /technical activities or processes, coordinate local team(s); guide development and implementation of new technologies.
- Provide scientific and technical guidance; actively foster knowledge exchange. Develop, mentor and coach other scientific associates; present scientific /technical results internally and contribute to publications, presentations and patents.
- Lead assigned teams; represent own technical function in teams and fulfill all project tasks and responsibilities related to the own discipline.
- Broadly use professional concepts in accordance with company objectives to solve complex problems in creative and effective ways.
- Contribute to many cost center goals and objectives; may contribute to service line goals.
- Responsible for providing scientific leadership and project management for multiple projects.
- Plan, coordinate, implement and take full responsibility for all designated tasks associated with Analytical R&D for the formulation development unit.
- Develop detailed plans and timelines, develop Analytical strategies and plans for designated projects from development to cGMP labs.
Minimum Requirement:
- Full time Doctorate in Pharmaceutical Sciences/Analytical or Organic Chemistry with 10+ years’ experience
- Operations Management and Execution
- Project Management
- Collaborating across boundaries
- Functional Breadth
- People Matters
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network
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? https://www.novartis.com/about/strategy/people-and-culture
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Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
Accessibility and accommodation
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
