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Global Manufacturing Sciences BioProcess Lead (Sr. Manager)(m/w/x)
Leading technical investigations for biologics drug substance manufacturing for therapies in immunology, oncology, and neuroscience. 10+ years biopharma development/manufacturing experience, with mammalian upstream/downstream process expertise required. Global coordination across manufacturing sites.
Requirements
- Bachelor’s degree in Engineering, Life Sciences, or related field
- 10+ years of experience in pharmaceutical/biopharmaceutical development and/or manufacturing
- Advanced degree (MS or PhD) preferred
- Technical experience in mammalian upstream and/or downstream drug substance process development
- Experience in a global, matrixed organization
- Ability to analyze complex technical problems and drive data-based decisions
- Experience contributing to regulatory filings for biologics
- Ability to lead cross-functional technical projects
- Strong interpersonal and communication skills
Tasks
- Provide technical expertise and leadership for biologics portfolio
- Ensure continuity of biologics drug substance manufacturing processes
- Serve as a subject matter expert in mammalian cell culture and antibody production
- Lead technical investigations and process improvement projects
- Partner with Manufacturing Sciences teams on process improvement projects
- Collaborate with Biologics Process Development on lifecycle management projects
- Shape and align CMC content for multi-site products
- Drive knowledge sharing across sites for consistent execution
- Propose and implement process improvements and lifecycle management initiatives
- Represent Bio Process Sciences on cross-functional governance teams
Work Experience
- 10 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- Chinese – Basic
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Global Manufacturing Sciences BioProcess Lead (Sr. Manager)(m/w/x)
Leading technical investigations for biologics drug substance manufacturing for therapies in immunology, oncology, and neuroscience. 10+ years biopharma development/manufacturing experience, with mammalian upstream/downstream process expertise required. Global coordination across manufacturing sites.
Requirements
- Bachelor’s degree in Engineering, Life Sciences, or related field
- 10+ years of experience in pharmaceutical/biopharmaceutical development and/or manufacturing
- Advanced degree (MS or PhD) preferred
- Technical experience in mammalian upstream and/or downstream drug substance process development
- Experience in a global, matrixed organization
- Ability to analyze complex technical problems and drive data-based decisions
- Experience contributing to regulatory filings for biologics
- Ability to lead cross-functional technical projects
- Strong interpersonal and communication skills
Tasks
- Provide technical expertise and leadership for biologics portfolio
- Ensure continuity of biologics drug substance manufacturing processes
- Serve as a subject matter expert in mammalian cell culture and antibody production
- Lead technical investigations and process improvement projects
- Partner with Manufacturing Sciences teams on process improvement projects
- Collaborate with Biologics Process Development on lifecycle management projects
- Shape and align CMC content for multi-site products
- Drive knowledge sharing across sites for consistent execution
- Propose and implement process improvements and lifecycle management initiatives
- Represent Bio Process Sciences on cross-functional governance teams
Work Experience
- 10 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- Chinese – Basic
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Takeda
Industry
Pharmaceuticals
Description
Das Unternehmen fokussiert sich darauf, lebensverändernde Therapien in den Bereichen Magen-Darm- und Entzündungskrankheiten, seltene Krankheiten, Onkologie, Neurowissenschaften und Impfstoffe zu entdecken und bereitzustellen.
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