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Engineering Site Lead / Director(m/w/x)
Leading engineering operations and cGMP compliance at a global biopharma site. Extensive pharmaceutical manufacturing leadership experience required. Annual bonus, shares and savings program.
Requirements
- Bachelor or Master of Engineering degree
- Extensive experience in pharmaceutical or related manufacturing & engineering industry
- Leadership expertise in multinational or matrix organization
- Fluency in English
- Knowledge of EHS, cGMP rules, standards, guidelines
- Excellent knowledge of legal framework, standards, regulations
- Leadership expertise
- Internal and external customer orientation, negotiation skills in multinational environment
- Ability to identify, avoid, eliminate business risks
- Confident, determined, courteous appearance towards business partners
- Fluency in German (preferred but not mandatory)
Tasks
- Lead the Engineering function at the Marburg site
- Ensure operational excellence and cGMP compliance
- Ensure Health, Safety, Environmental, and Sustainability compliance
- Shape strategy as a member of the Site Leadership Team
- Drive continuous improvement in Sustainability
- Drive continuous improvement in Facilities/Utilities
- Drive continuous improvement in Capital Projects
- Drive continuous improvement in Engineering Compliance
- Drive continuous improvement in Automation
- Drive continuous improvement in Production Engineering
- Lead and develop an efficient Engineering organization
- Align Engineering organization with GSK objectives
- Drive optimization of business processes within Engineering
- Drive optimization of business processes across cross-functional teams
- Oversee technical outsourcing
- Oversee service agreements
- Oversee resource allocation
- Manage CAPEX planning
- Manage OPEX planning
- Ensure project delivery meets timelines
- Ensure project delivery meets budget
- Review technical projects
- Assess technical projects
- Contribute to technical project approval processes
- Ensure compliance with internal standards
- Ensure compliance with legal standards
- Ensure compliance with regulatory standards
- Implement harmonized engineering processes
- Implement harmonized engineering documents
- Implement harmonized engineering tools
- Support global engineering initiatives
- Foster best practice sharing
- Fulfill delegated responsibilities under German law
- Fulfill delegated responsibilities under Marburg DH matrix
- Champion site risk management
- Champion continuous improvement
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Native
- German – Business Fluent
Tools & Technologies
- EHS
- cGMP
Benefits
Competitive Pay
- Competitive salary
- Shares and savings programme
Bonuses & Incentives
- Annual bonus
Healthcare & Fitness
- Healthcare and wellbeing programmes
Retirement Plans
- Pension plan membership
Flexible Working
- Hybrid working model
- Flexible work hours
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Engineering Site Lead / Director(m/w/x)
Leading engineering operations and cGMP compliance at a global biopharma site. Extensive pharmaceutical manufacturing leadership experience required. Annual bonus, shares and savings program.
Requirements
- Bachelor or Master of Engineering degree
- Extensive experience in pharmaceutical or related manufacturing & engineering industry
- Leadership expertise in multinational or matrix organization
- Fluency in English
- Knowledge of EHS, cGMP rules, standards, guidelines
- Excellent knowledge of legal framework, standards, regulations
- Leadership expertise
- Internal and external customer orientation, negotiation skills in multinational environment
- Ability to identify, avoid, eliminate business risks
- Confident, determined, courteous appearance towards business partners
- Fluency in German (preferred but not mandatory)
Tasks
- Lead the Engineering function at the Marburg site
- Ensure operational excellence and cGMP compliance
- Ensure Health, Safety, Environmental, and Sustainability compliance
- Shape strategy as a member of the Site Leadership Team
- Drive continuous improvement in Sustainability
- Drive continuous improvement in Facilities/Utilities
- Drive continuous improvement in Capital Projects
- Drive continuous improvement in Engineering Compliance
- Drive continuous improvement in Automation
- Drive continuous improvement in Production Engineering
- Lead and develop an efficient Engineering organization
- Align Engineering organization with GSK objectives
- Drive optimization of business processes within Engineering
- Drive optimization of business processes across cross-functional teams
- Oversee technical outsourcing
- Oversee service agreements
- Oversee resource allocation
- Manage CAPEX planning
- Manage OPEX planning
- Ensure project delivery meets timelines
- Ensure project delivery meets budget
- Review technical projects
- Assess technical projects
- Contribute to technical project approval processes
- Ensure compliance with internal standards
- Ensure compliance with legal standards
- Ensure compliance with regulatory standards
- Implement harmonized engineering processes
- Implement harmonized engineering documents
- Implement harmonized engineering tools
- Support global engineering initiatives
- Foster best practice sharing
- Fulfill delegated responsibilities under German law
- Fulfill delegated responsibilities under Marburg DH matrix
- Champion site risk management
- Champion continuous improvement
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Native
- German – Business Fluent
Tools & Technologies
- EHS
- cGMP
Benefits
Competitive Pay
- Competitive salary
- Shares and savings programme
Bonuses & Incentives
- Annual bonus
Healthcare & Fitness
- Healthcare and wellbeing programmes
Retirement Plans
- Pension plan membership
Flexible Working
- Hybrid working model
- Flexible work hours
About the Company
GSK
Industry
Pharmaceuticals
Description
GSK is a global biopharma company focused on preventing and treating diseases through innovation in specialty medicines and vaccines.
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