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Associate Director Science & Technology(m/w/x)
Drug product development for regulatory submissions at a global pharma research organization, focusing on oligonucleotide-based therapies. Expert knowledge in oligonucleotide drug product development and 3-6 years parenteral drug experience required. Strategic impact on global drug discovery.
Requirements
- Ph.D. in Pharmaceutical Sciences, Chemical engineering, Chemistry or related disciplines
- Minimum of 3 – 6 years of experience in parenteral drug development
- Experience with oligonucleotides (mRNA, siRNA, ASO)
- Master's degree with a minimum of 5 - 8 years of relevant experience
- Expert knowledge in the development of oligonucleotide drug products
- Ability to lead technology development programs
- Proactive problem-solver
- Experience driving digital transformation
Tasks
- Represent scientific and technical excellence in the drug product sub-team
- Author source documents for regulatory submissions
- Review CMC modules
- Lead and manage project and cross-functional team activities
- Drive long-term strategies in science and technology
- Generate and implement impactful procedures and guidelines across teams
- Scout, evaluate, and implement innovative drug delivery technologies in xRNA development
Work Experience
- 3 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
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Associate Director Science & Technology(m/w/x)
Drug product development for regulatory submissions at a global pharma research organization, focusing on oligonucleotide-based therapies. Expert knowledge in oligonucleotide drug product development and 3-6 years parenteral drug experience required. Strategic impact on global drug discovery.
Requirements
- Ph.D. in Pharmaceutical Sciences, Chemical engineering, Chemistry or related disciplines
- Minimum of 3 – 6 years of experience in parenteral drug development
- Experience with oligonucleotides (mRNA, siRNA, ASO)
- Master's degree with a minimum of 5 - 8 years of relevant experience
- Expert knowledge in the development of oligonucleotide drug products
- Ability to lead technology development programs
- Proactive problem-solver
- Experience driving digital transformation
Tasks
- Represent scientific and technical excellence in the drug product sub-team
- Author source documents for regulatory submissions
- Review CMC modules
- Lead and manage project and cross-functional team activities
- Drive long-term strategies in science and technology
- Generate and implement impactful procedures and guidelines across teams
- Scout, evaluate, and implement innovative drug delivery technologies in xRNA development
Work Experience
- 3 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
About the Company
Novartis Pharma AG
Industry
Pharmaceuticals
Description
The company is a global pharmaceutical research organization focused on discovering innovative new drugs that will change the practice of medicine.
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