BioNTech SE
Director Manufacturing Sciences & Technology(m/w/x)
Full-timeOn-siteSenior
Mainz
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BOBoehringer Ingelheim
Senior Commercial Process Manager(m/w/x)
Ingelheim am Rhein, Biberach
Full-timeOn-siteSenior
Nejo AI Summary
Shaping commercial manufacturing processes for innovative pharmaceuticals, including product launches and lifecycle support. Extensive pharmaceutical industry experience, including API manufacturing under cGMP, required. Support for product lifecycle management and interdisciplinary team leadership.
Requirements
- University degree with PhD in chemistry or related field
- Extensive experience in pharmaceutical industry (Operations, Regulatory Affairs, Drug Substance Development)
- Proven ability to lead cross-functional matrix teams internationally
- Strong project management expertise
- Practical experience in API manufacturing under cGMP conditions
- Practical experience in GMP process development
- Experience in solid-phase peptide synthesis is an advantage
- Experience in preparative HPLC is an advantage
- Experience in solid-phase oligonucleotide synthesis is an advantage
- Experience in ADCs is an advantage
- Strong regulatory and compliance expertise
- Team-oriented mindset
- Strategic thinking
- High level of commitment
- Flexibility
- Willingness to travel for business
- Very good command of English, written and spoken
- Several years of experience in international business environment
- Applications from persons with severe disabilities warmly welcomed
- Preferential consideration for severely disabled applicants in case of equal qualifications
Tasks
- Shape efficient commercial manufacturing processes
- Drive transfer of innovative pharmaceutical products
- Support products throughout their lifecycle
- Lead interdisciplinary project teams
- Prepare and execute product launches
- Manage technology transfers between sites
- Ensure manufacturing process compliance and change management
- Represent Drug Substance function in development departments
- Contribute to strategic initiatives for future improvements
- Ensure stable, cost-efficient, registration-compliant supply
- Maintain GMP-compliant supply to global markets
Work Experience
- approx. 4 - 6 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Tools & Technologies
- cGMP
- GMP
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Boehringer Ingelheim and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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BOBoehringer Ingelheim
Senior Commercial Process Manager(m/w/x)
Ingelheim am Rhein, Biberach
Full-timeOn-siteSenior
Nejo AI Summary
Shaping commercial manufacturing processes for innovative pharmaceuticals, including product launches and lifecycle support. Extensive pharmaceutical industry experience, including API manufacturing under cGMP, required. Support for product lifecycle management and interdisciplinary team leadership.
Requirements
- University degree with PhD in chemistry or related field
- Extensive experience in pharmaceutical industry (Operations, Regulatory Affairs, Drug Substance Development)
- Proven ability to lead cross-functional matrix teams internationally
- Strong project management expertise
- Practical experience in API manufacturing under cGMP conditions
- Practical experience in GMP process development
- Experience in solid-phase peptide synthesis is an advantage
- Experience in preparative HPLC is an advantage
- Experience in solid-phase oligonucleotide synthesis is an advantage
- Experience in ADCs is an advantage
- Strong regulatory and compliance expertise
- Team-oriented mindset
- Strategic thinking
- High level of commitment
- Flexibility
- Willingness to travel for business
- Very good command of English, written and spoken
- Several years of experience in international business environment
- Applications from persons with severe disabilities warmly welcomed
- Preferential consideration for severely disabled applicants in case of equal qualifications
Tasks
- Shape efficient commercial manufacturing processes
- Drive transfer of innovative pharmaceutical products
- Support products throughout their lifecycle
- Lead interdisciplinary project teams
- Prepare and execute product launches
- Manage technology transfers between sites
- Ensure manufacturing process compliance and change management
- Represent Drug Substance function in development departments
- Contribute to strategic initiatives for future improvements
- Ensure stable, cost-efficient, registration-compliant supply
- Maintain GMP-compliant supply to global markets
Work Experience
- approx. 4 - 6 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Tools & Technologies
- cGMP
- GMP
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Boehringer Ingelheim and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Boehringer Ingelheim
Industry
Pharmaceuticals
Description
The company is focused on delivering lasting value to patients through innovative therapies and early clinical development.
Not a perfect match?
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