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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
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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