摘要
About the Role
Major Accountabilities:
•Design, plan and perform scientific experiments for projects at different clinical phases of drug substance and drug product with minimal guidance.
Monitors degradation pathways and shelf-life of products.
Well versed with regulatory guidelines, scientific literature, technology transfer and interpretation of the results to draw conclusions in reports.
•Adhere to Quality metrics, Compliance and Good Documentation Practices following ALCOA+ principles, GLP, OQM, HSE, ISEC and Novartis guidelines.
•Should be a Team player by adding value in collaborating with other teams to support project deliverables within agreed timelines, mentoring new joiners, active participation in project meetings / networks / meetings and contributing to Team goals while meeting individual objectives.
•Responsible for Qualification of instruments / equipment’s (URS to Report) and periodic calibrations as per applicable site procedures.
Responsible for implementation and maintenance of lean/efficient/environmentally sustainable practices in the laboratory
•Ability to perform investigations, guide team members, communicate proactively and clearly to global stakeholders.
Cross-functional collaboration
What you bring to the role:
•Broad scientific or technical knowledge in a specific area.
•Adequate understanding of development processes in own function.
•Advanced knowledge of laboratory and/or technical tools.
•Good knowledge of software and computer tools.
•Proficient in literature searches
Good understanding about Regulatory Guidelines
Strong problem-solving and critical thinking
Knowledge on ICH guidelines (Q2(R1)), QbD principles etc
Minimum requirements:
•Minimum: M. Pharm./M.Sc. Good knowledge of English (oral and written).
•PhD on technical subject with 4+yrs of relevant experience. or Master of Science with 12+ years of relevant experience in testing of Solid oral dosage forms.
•Good presentation skills and scientific/technical writing skills.
•Good communication skills
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.
