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(Senior) Program Manager, Integrated Biologics(m/w/x)
Leading customer programs from tech transfer to GMP manufacturing for biologics. Strong understanding of GMP and drug substance development required. Relocation assistance, agile career path.
Requirements
- Degree in Chemistry, Biology, Biotechnology, or related field
- Project or program management experience in pharma or CDMO
- Strong understanding of technical, commercial, and organizational factors
- Ability to lead cross-functional teams and deliver complex programs
- Knowledge of GMP manufacturing and drug substance development
- Excellent communication, collaboration, and leadership skills
- Fluent English
Tasks
- Lead and deliver customer programs from technology transfer to GMP manufacturing and project closure
- Ensure quality, timelines, and cost-effectiveness of projects
- Act as the main point of contact for customers, fostering transparent communication and long-term collaboration
- Inspire and coordinate cross-functional teams in a matrix environment
- Promote shared ownership and high performance within teams
- Manage program scope, timelines, and financials
- Align project activities with strategic business goals
- Collaborate across functions to manage scope changes and support commercial strategies
- Contribute to future business opportunities
- Identify and proactively address project risks
- Ensure smooth issue resolution and continuous improvement
- Mentor and support team members
- Foster a culture of learning, inclusion, and professional development
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Benefits
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
- Inclusive workplace
Purpose-Driven Work
- Ethical workplace
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(Senior) Program Manager, Integrated Biologics(m/w/x)
Leading customer programs from tech transfer to GMP manufacturing for biologics. Strong understanding of GMP and drug substance development required. Relocation assistance, agile career path.
Requirements
- Degree in Chemistry, Biology, Biotechnology, or related field
- Project or program management experience in pharma or CDMO
- Strong understanding of technical, commercial, and organizational factors
- Ability to lead cross-functional teams and deliver complex programs
- Knowledge of GMP manufacturing and drug substance development
- Excellent communication, collaboration, and leadership skills
- Fluent English
Tasks
- Lead and deliver customer programs from technology transfer to GMP manufacturing and project closure
- Ensure quality, timelines, and cost-effectiveness of projects
- Act as the main point of contact for customers, fostering transparent communication and long-term collaboration
- Inspire and coordinate cross-functional teams in a matrix environment
- Promote shared ownership and high performance within teams
- Manage program scope, timelines, and financials
- Align project activities with strategic business goals
- Collaborate across functions to manage scope changes and support commercial strategies
- Contribute to future business opportunities
- Identify and proactively address project risks
- Ensure smooth issue resolution and continuous improvement
- Mentor and support team members
- Foster a culture of learning, inclusion, and professional development
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Benefits
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
- Inclusive workplace
Purpose-Driven Work
- Ethical workplace
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Lonza
Industry
Pharmaceuticals
Description
Lonza is a global leader in life sciences, committed to improving lives through innovative solutions and ethical practices.
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