Description:

 
335023BR
Mar 31, 2022
USA

Job Description

12,000. The number of associates worldwide working together to reimagine medicine!

What you'll be doing:
• Advances complex downstream process development efforts as a technical lead within a cross-functional team across sites.
• Independently designs and executes gene therapy downstream process development studies.
• Performs experiments at both large-scale and small-scale to support pre-clinical, clinical and commercial programs. Ensures these experiments are done in a timely fashion with high quality.
• Stays current with the latest scientific and engineering developments in the field.
• Leverages strong understanding of biologics downstream process to evaluate and introduces new technologies and innovative ideas related to downstream process development.
• Analyzes and interprets experimental data from process studies with strong statistical mindset. Makes decisions based on statistically sound conclusions. Presents study results internally and externally in a cross-functional setting.
• Independently authors technical reports of studies of process development activities and laboratory experiments, such as development report, study report, investigational summary report, etc.
• Collaborates with cross-functional groups to advance pipeline programs. Provides support for regulatory filings and author sections in IND filings.

Diversity & Inclusion / EEO

The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.

Minimum Requirements

What you'll bring:
• Bachelor's, biological sciences, pharmaceutical sciences or related technical field with 8 years relevant experience or Master's with 6 or PHD with 4.
• Comprehensive experience with a variety of biopharmaceutical purification processes such as chromatographic separation, depth filtration, precipitation & flocculation, tangential flow filtration, adventitious viral clearance, ultracentrifugation, and impurity clearance.
• Proficient in statistical analysis principles and approaches. Working knowledge and experience with Design of Experiment (DoE).
• Ability to analyze data to make date-driven decisions and further progress development strategies.
• Proven team leader with previous experience of effectively leading technical group.
• Innovative with a continuous improvement mindset.
• Good communication skills with project management experience in cross-functional setting.
• Knowledge of current Good Manufacturing Practices (cGMP) requirements and their indication in process development environment.
• Knowledge of viral gene therapy and previous experience with AAV downstream process development is preferred

Why Novartis?
766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.
We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.
We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!
Imagine what you could do here at Novartis!

Commitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Accessibility and reasonable accommodations
The Novartis Group of Companies are 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 application process, or in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

https://www.novartis.com/careers/careers-research/notice-all-applicants-us-job-openings
Global Drug Development
TECHNICAL R & D GDD
USA
San Diego, CA
Research & Development
Full Time
Regular
No

About Novartis:

Our purpose is to reimagine medicine to improve and extend people's lives. We use innovative science and technology to address some of society's most challenging healthcare issues. We discover and develop breakthrough treatments and find new ways to deliver them to as many people as possible. We also aim to reward those who invest their money, time and ideas in our company. For more information on career opportunities at Novartis, visit: https://www.novartis.com/careers. Join our Talent Pool by visiting https://talentnetwork.novartis.com/careerfair?projectId=94&source=Career+Fair&tags=sacc.dc.2022

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