Your personal AI career agent
Global Head of Quality Systems(m/w/x)
Governing data integrity and QMS architecture for specialty pharmaceuticals. Master's degree and GxP leadership experience required. Work from EU country (2 months/year), 30 days holiday.
Requirements
- Master's degree in natural science, pharmaceutical or GxP background
- Disciplinary and functional leadership experience in regulated GxP environments
- Expertise in QMS design, eQMS platforms, data integrity governance, global regulatory compliance
- Analytical and strategic thinking for quality risk assessment and improvement
- Experience collaborating with regulatory authorities and managing external partners
- Familiarity with science IT systems, CSV, digital quality management tools
- Master's degree in natural science, pharmaceutical or GxP background
Tasks
- Ensure robust, compliant Quality Management System
- Lead CP quality interfaces and system architecture
- Govern data integrity for consistency and reliability
- Develop global cross-functional organization
- Allocate resources and plan budgets
- Act as central escalation point (SPOC)
- Design and implement Quality Management System
- Continuously improve core processes (Deviation, CAPA, Change Control, Management Review)
- Ensure compliant, future-ready quality system architecture
- Select, maintain, and evaluate eQMS solutions
- Align IT systems with Science Function
- Govern data integrity across systems and documentation
- Oversee computerized system validation (CSV)
- Ensure compliance with global regulatory requirements
- Lead quality governance initiatives
- Enhance system effectiveness with improvement programs
- Foster cross-functional alignment across departments
- Engage with regulatory authorities, CMOs, suppliers, and external partners
- Design and implement training programs
- Develop internal team capabilities
Work Experience
- 10 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- eQMS platforms
- GxP
- GMP
- GVP
- GCP
- QMS
- CSV
Benefits
Flexible Working
- Customizable working models
- Working time account
Workation & Sabbatical
- Work from EU country (2 months/year)
More Vacation Days
- Compensatory time off
- 30 days of holiday
Additional Allowances
- Flexible benefits budget
- Subsidies for meal costs
Retirement Plans
- Increased company pension provision
Healthcare & Fitness
- Fitness and health offers
Public Transport Subsidies
- Subsidies for travel costs
Corporate Discounts
- Corporate benefits platform with discounts
Learning & Development
- Tailored training courses
Team Events
- Company and team events
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
Not a perfect match?
- CHEPLAPHARM Arzneimittel GmbHFull-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen
- CHEPLAPHARM Arzneimittel GmbH
Global Head of Knowledge Hub(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Product Operations(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Regulatory Affairs(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Science Affiliates(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen
Global Head of Quality Systems(m/w/x)
Governing data integrity and QMS architecture for specialty pharmaceuticals. Master's degree and GxP leadership experience required. Work from EU country (2 months/year), 30 days holiday.
Requirements
- Master's degree in natural science, pharmaceutical or GxP background
- Disciplinary and functional leadership experience in regulated GxP environments
- Expertise in QMS design, eQMS platforms, data integrity governance, global regulatory compliance
- Analytical and strategic thinking for quality risk assessment and improvement
- Experience collaborating with regulatory authorities and managing external partners
- Familiarity with science IT systems, CSV, digital quality management tools
- Master's degree in natural science, pharmaceutical or GxP background
Tasks
- Ensure robust, compliant Quality Management System
- Lead CP quality interfaces and system architecture
- Govern data integrity for consistency and reliability
- Develop global cross-functional organization
- Allocate resources and plan budgets
- Act as central escalation point (SPOC)
- Design and implement Quality Management System
- Continuously improve core processes (Deviation, CAPA, Change Control, Management Review)
- Ensure compliant, future-ready quality system architecture
- Select, maintain, and evaluate eQMS solutions
- Align IT systems with Science Function
- Govern data integrity across systems and documentation
- Oversee computerized system validation (CSV)
- Ensure compliance with global regulatory requirements
- Lead quality governance initiatives
- Enhance system effectiveness with improvement programs
- Foster cross-functional alignment across departments
- Engage with regulatory authorities, CMOs, suppliers, and external partners
- Design and implement training programs
- Develop internal team capabilities
Work Experience
- 10 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- eQMS platforms
- GxP
- GMP
- GVP
- GCP
- QMS
- CSV
Benefits
Flexible Working
- Customizable working models
- Working time account
Workation & Sabbatical
- Work from EU country (2 months/year)
More Vacation Days
- Compensatory time off
- 30 days of holiday
Additional Allowances
- Flexible benefits budget
- Subsidies for meal costs
Retirement Plans
- Increased company pension provision
Healthcare & Fitness
- Fitness and health offers
Public Transport Subsidies
- Subsidies for travel costs
Corporate Discounts
- Corporate benefits platform with discounts
Learning & Development
- Tailored training courses
Team Events
- Company and team events
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
CHEPLAPHARM Arzneimittel GmbH
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein globales und wachsendes Specialty Pharmaunternehmen mit einem außergewöhnlichen, nachhaltigen Geschäftsmodell.
Not a perfect match?
- CHEPLAPHARM Arzneimittel GmbH
Global Head of Quality(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Knowledge Hub(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Product Operations(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Regulatory Affairs(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Science Affiliates(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen