J. Wagner GmbH
SAP Program Manager(m/w/x)
Full-time/Part-timeWith HomeofficeSenior
Markdorf
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EUEurofins
GMP Project Manager Pharma(m/w/x)
Konstanz
Full-timeWith Home OfficeExperienced
Nejo AI Summary
You will drive pharmaceutical projects from start to finish, balancing technical document approval with LIMS configuration to ensure analytical services meet the highest GMP standards.
Requirements
- Degree in life sciences or vocational training with 3+ years experience
- Experience in pharmaceutical QC or analytical development
- Strong customer orientation and confident communication
- Very good IT literacy and Office skills
- Demonstrated project management capability
- Excellent organizational and problem-solving skills
- High responsibility, reliability, and team spirit
- Very good German and good English
Tasks
- Lead end-to-end Pharma Analytics projects
- Manage analytical development and method validation
- Oversee dissolution, chromatography, and particle testing
- Coordinate stability storage and subcontracted services
- Define project plans and track milestones
- Manage purchase orders and project risks
- Report project status to stakeholders
- Review and approve technical documents and results
- Ensure GMP compliance for analytical work
- Contribute to audit readiness and continuous improvement
- Map and configure projects within LIMS
- Support data integrity best practices
- Coordinate interfaces between labs, clients, and partners
- Support the acquisition of new projects
- Author and maintain SOPs and GMP documentation
- Assist with client and regulatory audits
- Implement improvements to increase site efficiency
Work Experience
3 years
Education
Vocational certificationORBachelor's degree
Languages
German – Business FluentEnglish – Business Fluent
Tools & Technologies
ISO 17025GLPGMPOfficeLIMSPMPIPMA
Benefits
Flexible Working
- •Flexible working hours
- •Partial remote work
Learning & Development
- •Professional development opportunities
- •Training and certifications
Career Advancement
- •Internal mobility opportunities
Diverse Work
- •International project exposure
Modern Equipment
- •Modern workplace and tools
Competitive Pay
- •Competitive compensation
Other Benefits
- •Attractive social benefits
Informal Culture
- •Inclusive culture
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Eurofins 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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EUEurofins
GMP Project Manager Pharma(m/w/x)
Konstanz
Full-timeWith Home OfficeExperienced
Nejo AI Summary
You will drive pharmaceutical projects from start to finish, balancing technical document approval with LIMS configuration to ensure analytical services meet the highest GMP standards.
Requirements
- Degree in life sciences or vocational training with 3+ years experience
- Experience in pharmaceutical QC or analytical development
- Strong customer orientation and confident communication
- Very good IT literacy and Office skills
- Demonstrated project management capability
- Excellent organizational and problem-solving skills
- High responsibility, reliability, and team spirit
- Very good German and good English
Tasks
- Lead end-to-end Pharma Analytics projects
- Manage analytical development and method validation
- Oversee dissolution, chromatography, and particle testing
- Coordinate stability storage and subcontracted services
- Define project plans and track milestones
- Manage purchase orders and project risks
- Report project status to stakeholders
- Review and approve technical documents and results
- Ensure GMP compliance for analytical work
- Contribute to audit readiness and continuous improvement
- Map and configure projects within LIMS
- Support data integrity best practices
- Coordinate interfaces between labs, clients, and partners
- Support the acquisition of new projects
- Author and maintain SOPs and GMP documentation
- Assist with client and regulatory audits
- Implement improvements to increase site efficiency
Work Experience
3 years
Education
Vocational certificationORBachelor's degree
Languages
German – Business FluentEnglish – Business Fluent
Tools & Technologies
ISO 17025GLPGMPOfficeLIMSPMPIPMA
Benefits
Flexible Working
- •Flexible working hours
- •Partial remote work
Learning & Development
- •Professional development opportunities
- •Training and certifications
Career Advancement
- •Internal mobility opportunities
Diverse Work
- •International project exposure
Modern Equipment
- •Modern workplace and tools
Competitive Pay
- •Competitive compensation
Other Benefits
- •Attractive social benefits
Informal Culture
- •Inclusive culture
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Eurofins 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
Eurofins
Industry
Pharmaceuticals
Description
Das Unternehmen ist die führende Labor-Gruppe weltweit für Analyse- und Serviceleistungen in der Lebensmittel-, Pharma-, Umwelt- und Konsumgüterindustrie.
Not a perfect match?
- J. Wagner GmbH
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Full-timeWith HomeofficeSeniorNürnberg, Konstanz - BLACKROLL®
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Consultant SAP PS (Project System) & Project Management(m/w/x)
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