Bavarian Nordic Berna GmbH
Project Manager Engineering - CAPEX(m/w/x)
Full-timeOn-siteSenior
Bern
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Leading large-scale biotherapeutic production capacity projects from strategy to licensing at a global biotherapeutics leader. 10+ years pharmaceutical engineering or manufacturing experience with large-scale E2E program delivery required. Global program coordination across manufacturing and validation sites.
Requirements
- Degree in Mechanical, Electrical, Chemical Engineering or equivalent
- 10+ years pharmaceutical engineering or manufacturing experience
- Track record delivering large-scale E2E programmes
- Experience in Front-End-Loading (FEL)
- Understanding of cGMPs, Validation, and C&Q
- Knowledge of GEP and EHS-by-design
- Financial management of multi-million dollar investments
- Exceptional communication and remote team leadership
- Ability to navigate technical and regulatory challenges
- PMP or Professional Engineer (P.E.) certification
Tasks
- Translate strategic investments into physical production capacity
- Lead the project lifecycle from front-end-loading to licensing
- Align project decisions with global strategic goals
- Connect global engineering strategy with site-level delivery
- Coordinate large-scale programs across manufacturing and validation
- Integrate regulatory functions into project execution
- Manage cross-functional teams and remove operational roadblocks
- Convert conceptual definitions into executable plans
- Establish clear project timelines and budgets
- Direct daily activities for process engineering teams
- Oversee design, construction, and operational readiness
- Maintain accountability for ROI and capital budgeting
- Negotiate contracts to align with project value
- Evaluate technical interdependencies and mitigate risks
- Ensure adherence to safety and execution standards
- Present strategic recommendations to corporate leadership
Work Experience
- 10 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- Front-End-Loading (FEL)
- cGMPs
- Validation principles
- C&Q
- GEP
- EHS-by-design
- PMP
- Professional Engineer (P.E.)
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring 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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Leading large-scale biotherapeutic production capacity projects from strategy to licensing at a global biotherapeutics leader. 10+ years pharmaceutical engineering or manufacturing experience with large-scale E2E program delivery required. Global program coordination across manufacturing and validation sites.
Requirements
- Degree in Mechanical, Electrical, Chemical Engineering or equivalent
- 10+ years pharmaceutical engineering or manufacturing experience
- Track record delivering large-scale E2E programmes
- Experience in Front-End-Loading (FEL)
- Understanding of cGMPs, Validation, and C&Q
- Knowledge of GEP and EHS-by-design
- Financial management of multi-million dollar investments
- Exceptional communication and remote team leadership
- Ability to navigate technical and regulatory challenges
- PMP or Professional Engineer (P.E.) certification
Tasks
- Translate strategic investments into physical production capacity
- Lead the project lifecycle from front-end-loading to licensing
- Align project decisions with global strategic goals
- Connect global engineering strategy with site-level delivery
- Coordinate large-scale programs across manufacturing and validation
- Integrate regulatory functions into project execution
- Manage cross-functional teams and remove operational roadblocks
- Convert conceptual definitions into executable plans
- Establish clear project timelines and budgets
- Direct daily activities for process engineering teams
- Oversee design, construction, and operational readiness
- Maintain accountability for ROI and capital budgeting
- Negotiate contracts to align with project value
- Evaluate technical interdependencies and mitigate risks
- Ensure adherence to safety and execution standards
- Present strategic recommendations to corporate leadership
Work Experience
- 10 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- Front-End-Loading (FEL)
- cGMPs
- Validation principles
- C&Q
- GEP
- EHS-by-design
- PMP
- Professional Engineer (P.E.)
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring 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
CSL Behring
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein globaler Marktführer in der Biotherapeutik, der innovative Therapien für Patienten mit immunologischen, hämatologischen, kardiovaskulären und anderen Erkrankungen entwickelt.
Not a perfect match?
- Bavarian Nordic Berna GmbH
Project Manager Engineering - CAPEX(m/w/x)
Full-timeOn-siteSeniorBern - CSL Behring
Senior Engineer (Drug Delivery Lead)(m/w/x)
Full-timeOn-siteManagementBern - Bavarian Nordic Berna GmbH
Project Manager Engineering - Pharma & Biotech(m/w/x)
Full-timeOn-siteExperiencedBern - CSL Behring
Production Engineer Aseptic Processes(m/w/x)
Full-timeOn-siteExperiencedBern - CSL Behring
Associate Director, Quality Assurance Support(m/w/x)
Full-timeOn-siteSeniorBern