CHEPLAPHARM Arzneimittel GmbH
Global Head of Pharmacovigilance(m/w/x)
Full-timeWith HomeofficeSenior
Greifswald, Berlin, Binningen
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CHCHEPLAPHARM Arzneimittel GmbH
Senior Portfolio Owner Pharmacovigilance(m/w/x)
Greifswald, Berlin, Binningen
Full-timeWith Home OfficeSenior
Nejo AI Summary
End-to-end ownership of pharmacovigilance product strategy for global pharmaceutical brand availability. 8+ years in pharmacovigilance and 10+ years leadership experience required. Work from EU country (2 months/year), 30 days holiday.
Requirements
- Master’s degree in scientific or related discipline
- 10+ years professional and leadership experience in complex, matrixed, cross-functional organizations
- 8+ years professional experience in Pharmacovigilance
- Proven ability to lead teams in complex environments
- Effective coordination across departments and stakeholders
- Strong leadership and communication skills
- Ability to motivate teams and build relationships
- Ability to evaluate solution approaches
- Work within partially defined frameworks
- Develop robust concepts based on market practices
- Experience handling complex, uncertain problem situations
- Decision-making based on incomplete information
- High degree of autonomy in adapting processes
- Achieve operational and strategic objectives
Tasks
- Provide end-to-end ownership of pharmacovigilance product-related activities
- Ensure strong product strategy for compliance, availability, and patient safety
- Act as central point of accountability and escalation
- Coordinate operations and provide leadership to the product team
- Organize and prioritize work
- Foster cross-functional alignment
- Involve relevant experts when needed
- Ensure effective collaboration and high-quality outcomes
- Manage core pharmacovigilance activities
- Process cases and assess causality and labeledness
- Detect signals and evaluate safety
- Mitigate risks and manage crises
- Implement risk management measures
- Deliver regulatory requirements (e.g., PSURs, safety variations)
- Align with global GVP requirements
- Define and drive global product safety strategy
- Integrate safety insights into product lifecycle
- Ensure regulatory PV compliance
- Prepare for inspections
- Align with global health authority expectations
- Provide disciplinary and functional leadership to PV team
- Allocate resources and manage budget
- Prioritize tasks and develop capabilities
- Make final decisions
- Align with internal stakeholders (e.g., SCM, Therapeutic Areas, Quality, Regulatory)
- Act as central escalation point (SPOC)
- Manage external partners, vendors, and service providers
- Monitor global regulatory developments
- Evaluate new PV tools and processes
- Drive continuous improvement of safety systems and methodologies
- Collaborate with medical and scientific functions
Work Experience
- 10 years
Education
- Master's degree
Languages
- English – Business Fluent
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
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CHEPLAPHARM Arzneimittel GmbH 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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CHCHEPLAPHARM Arzneimittel GmbH
Senior Portfolio Owner Pharmacovigilance(m/w/x)
Greifswald, Berlin, Binningen
Full-timeWith Home OfficeSenior
Nejo AI Summary
End-to-end ownership of pharmacovigilance product strategy for global pharmaceutical brand availability. 8+ years in pharmacovigilance and 10+ years leadership experience required. Work from EU country (2 months/year), 30 days holiday.
Requirements
- Master’s degree in scientific or related discipline
- 10+ years professional and leadership experience in complex, matrixed, cross-functional organizations
- 8+ years professional experience in Pharmacovigilance
- Proven ability to lead teams in complex environments
- Effective coordination across departments and stakeholders
- Strong leadership and communication skills
- Ability to motivate teams and build relationships
- Ability to evaluate solution approaches
- Work within partially defined frameworks
- Develop robust concepts based on market practices
- Experience handling complex, uncertain problem situations
- Decision-making based on incomplete information
- High degree of autonomy in adapting processes
- Achieve operational and strategic objectives
Tasks
- Provide end-to-end ownership of pharmacovigilance product-related activities
- Ensure strong product strategy for compliance, availability, and patient safety
- Act as central point of accountability and escalation
- Coordinate operations and provide leadership to the product team
- Organize and prioritize work
- Foster cross-functional alignment
- Involve relevant experts when needed
- Ensure effective collaboration and high-quality outcomes
- Manage core pharmacovigilance activities
- Process cases and assess causality and labeledness
- Detect signals and evaluate safety
- Mitigate risks and manage crises
- Implement risk management measures
- Deliver regulatory requirements (e.g., PSURs, safety variations)
- Align with global GVP requirements
- Define and drive global product safety strategy
- Integrate safety insights into product lifecycle
- Ensure regulatory PV compliance
- Prepare for inspections
- Align with global health authority expectations
- Provide disciplinary and functional leadership to PV team
- Allocate resources and manage budget
- Prioritize tasks and develop capabilities
- Make final decisions
- Align with internal stakeholders (e.g., SCM, Therapeutic Areas, Quality, Regulatory)
- Act as central escalation point (SPOC)
- Manage external partners, vendors, and service providers
- Monitor global regulatory developments
- Evaluate new PV tools and processes
- Drive continuous improvement of safety systems and methodologies
- Collaborate with medical and scientific functions
Work Experience
- 10 years
Education
- Master's degree
Languages
- English – Business Fluent
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
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CHEPLAPHARM Arzneimittel GmbH 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.
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
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