摘要
About the Role
Major accountabilities:
1. Plan, organize, execute, and document scientific experiments (e.g., analytical
method developments/ validations/ transfers/ stability/ release testing,
formulation development analytics etc.) according to the agreed timelines and
appropriate quality standards.
2. Accountable for documentation and submission of raw data in appropriate data
system (for e.g., LIMS test activation and results entry).
3. Responsible for good documentation practices (GDP) and good laboratory
practices (GLP) during execution of laboratory activities.
4. Support in evaluation and interpretation of results including investigations on
SST failures, OOX/Deviations/Change controls as needed.
5. Responsible for assigned laboratory related area/activities (e.g.,
chemical/reagents/consumables/samples/column/ glassware management
etc.).
6. Responsible for implementation and maintenance of
lean/efficient/environmentally sustainable practices in the laboratory.
7. Proactively communicate key issues and any other critical topics in a timely
manner to the manager and/or to any other relevant project team member(s).
8. Responsible to meet KQI (Key quality indicators) and KPI (Key performance
indicators) for all assigned activities.
9. Support internal and external audits and ensure no critical findings within the
assigned scope.
10. Actively contribute to team and organization goals.
11. Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISRM & Novartis
Guidelines.
12. Additional specific roles/tasks: See Up4Growth training assignments for the business roles for the associate
as per the team matrix and completion of trainings in transcript of learning
system (e.g., Up4Growth).
Minimum Requirements:
- Technician or Bachelors/Masters in Life Science (e.g., analytical / organic chemistry / pharmacy / pharmaceutical development) or equivalent.
- Knowledge in quality principles driving drug development such as GMP.
- Understanding of general regulatory and quality expectations.
- Good scientific background, communication skills including presentation and scientific/technical writing.
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
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: https://talentnetwork.novartis.com/network
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.
