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Process Engineer Small Molecules API Process Science (Associate Director)(m/w/x)
Process engineering for small molecules API platforms, integrating mechanistic modelling and process simulation at a biopharmaceutical company. MS/PhD in Chemical/Process/Pharmaceutical Engineering and 5+ years cGMP experience required. Focus on developing life-changing therapies for rare diseases and oncology.
Requirements
- MS/PhD in Chemical, Process, or Pharmaceutical Engineering
- At least 5 years cGMP environment experience
- Ideally 5 years small molecules pharmaceutical experience
- Self-motivation, interpersonal skills, and problem-solving
- Strategic enterprise thinking and innovative mindset
- Ability to inspire and enable people
- Priority focus and superior results delivery
- Capability elevation for present and future
Tasks
- Provide process engineering support for API platforms
- Apply chemical engineering and process chemistry fundamentals
- Integrate mechanistic modelling and process simulation
- Enhance process understanding through data analysis
- Identify and implement continuous improvement opportunities
- Support marketing applications for global markets
- Respond to inquiries from global health authorities
- Lead the Global Process Science team
- Serve as the company's small molecule API expert
- Manage technology transfers with internal and external sites
- Oversee process characterization and validation activities
- Conduct risk assessments and manage manufacturing costs
- Direct projects within the development and commercial portfolio
- Implement manufacturing strategies for key products
- Establish procedures for commercial technology transfer
- Facilitate knowledge sharing across global manufacturing sites
- Collaborate with quality, regulatory, and technical functions
- Define the vision for manufacturing technology projects
- Align local organizations with global manufacturing strategies
- Investigate process issues using root cause analysis
- Deliver sustainable corrective and preventative actions
- Provide expert support for due diligence and licensing
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- cGMP
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Process Engineer Small Molecules API Process Science (Associate Director)(m/w/x)
Process engineering for small molecules API platforms, integrating mechanistic modelling and process simulation at a biopharmaceutical company. MS/PhD in Chemical/Process/Pharmaceutical Engineering and 5+ years cGMP experience required. Focus on developing life-changing therapies for rare diseases and oncology.
Requirements
- MS/PhD in Chemical, Process, or Pharmaceutical Engineering
- At least 5 years cGMP environment experience
- Ideally 5 years small molecules pharmaceutical experience
- Self-motivation, interpersonal skills, and problem-solving
- Strategic enterprise thinking and innovative mindset
- Ability to inspire and enable people
- Priority focus and superior results delivery
- Capability elevation for present and future
Tasks
- Provide process engineering support for API platforms
- Apply chemical engineering and process chemistry fundamentals
- Integrate mechanistic modelling and process simulation
- Enhance process understanding through data analysis
- Identify and implement continuous improvement opportunities
- Support marketing applications for global markets
- Respond to inquiries from global health authorities
- Lead the Global Process Science team
- Serve as the company's small molecule API expert
- Manage technology transfers with internal and external sites
- Oversee process characterization and validation activities
- Conduct risk assessments and manage manufacturing costs
- Direct projects within the development and commercial portfolio
- Implement manufacturing strategies for key products
- Establish procedures for commercial technology transfer
- Facilitate knowledge sharing across global manufacturing sites
- Collaborate with quality, regulatory, and technical functions
- Define the vision for manufacturing technology projects
- Align local organizations with global manufacturing strategies
- Investigate process issues using root cause analysis
- Deliver sustainable corrective and preventative actions
- Provide expert support for due diligence and licensing
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- cGMP
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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