摘要
About the Role
Your responsibilities include, but are not limited to:
1. Meet quality, quantity and timelines in all assigned projects; Perform and document scientific experiments ; Plan & organize scientific experiments under minimal guidance from more experienced team members. Seeks proactively for support and coaching from Project Leader, Scientific Expert or other team members during the whole process if necessary. (I)
2. Provide documentation of raw data (I) ;evalsuate and Contribute to interpretation and report results under minimal guidance from more experienced team members. (I) ; Propose and provide input for the design of next experiments. (I); Optimize existing methods (lab or plant) or contribute to new method development and reproduce published methods and develop more efficient ones. (I)
3. Generate lab procedures, reports and/or instructions and/or SOP’s. (I, N) ; Actively transfer procedures/instructions to pilot plant or production, including troubleshooting, process steering controls etc. (I) ; Communicate and address problems, perform safety and literature searches under moderate guidance from more experienced team member. (I)
4. Keep record of and manage chemicals, intermediates, excipients and solvents within own area of responsibility. (I)
5. Collaborate with other team members to facilitate deliveries of DS and/or DP. (I) ; Act as mentors for new joinees.
6. Utilize special tools/equipments and/or specialized facilities e.g., containment/sterile labs. (I) ; evalsuate new lab equipment. (I) ; Schedule and perform routine maintenance and calibration of lab instruments/equipment & contribute to maintenance of infrastructure/equipment. (I)
7. Actively participate in project teams/meetings/networks. (I) ; Actively contributes to team goals. (I)
8. Ensure all own activities are aligned with overall drug development process. Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISEC & Novartis Guidelines ;Strategic and scientific contribution to Networks, target achievements according to net-work charter and annual objectives (I)
WHAT YOU’LL BRING TO THE ROLE:
- PhD on technical subject with 4yrs of relevant experience. or Master of Science with 8+ years of relevant experience Fluency in English language.
- Awareness for safe handling of chemicals, potentially dangerous materials and equipment. Broad theoretical and scientific knowledge in the relevant area (e.g. manufacturing, analytical, pharmaceutical).
- Skilled scientist with expertise in gas chromatography-based quantification methods using various detectors including GC-FID.
- Experience on dealing OOS/OOE and deviations involving above mentioned analytical techniques
- Proficient with laboratory and/or technical tools. Good knowledge of software and computer tools. Good documentation skills.
- Good knowledge of current Good Manufacturing Practices (cGMP) ;Advanced scientific/technical writing skills Wide experience on de-formulation studies of the drug products , especially in the microscopic evalsuation of drug component.
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
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.
