You ensure safety compliance and regulatory readiness by managing documentation, conducting inspections, and overseeing CAPAs, while continuously improving processes in the pharmacovigilance department.
Anforderungen
- •Advanced degree in life sciences
- •Expert knowledge of pharmacovigilance regulations
- •At least 5 years in Pharmacovigilance
- •Experience with GxP audits and inspections
- •Expertise in authoring procedural documents
- •Proactive, solution-oriented mindset
- •Ability to work in cross-functional teams
- •Good communication skills
- •Fluency in written and spoken English
- •Ability to accept shared responsibility
Deine Aufgaben
- •Oversee safety compliance tracking and reporting.
- •Manage and update safety procedural documents.
- •Ensure alignment with quality standards and regulations.
- •Perform process gap assessments and implement risk registers.
- •Support safety compliance and inspection readiness activities.
- •Prepare for and follow up on GxP inspections and audits.
- •Conduct mock inspections and lessons learned sessions.
- •Process and document non-conformities and CAPAs.
- •Monitor and analyze deviations and CAPAs.
- •Act as contact person for Veeva module issue management.
- •Support regulatory intelligence and improve procedural documents.
Deine Vorteile
Flexible hours
Vacation account
Digital learning
Performance development
Leadership development
Apprenticeships
LinkedIn Learning
Voice at the table
Equal culture
Opportunities to shape impact
Support for potential
Company bike
Job ticket
Deutschlandticket
Employer-funded pension
Childcare
Original Beschreibung
# Associate Director PV Compliance (m/w/d)
Mainz, Germany; London, United Kingdom; Munich, Germany | full time | Job ID: 9214
The Associate Director Safety Compliance performs specific duties in the Medical Safety & Pharmacovigilance (MSPv) department to ensure compliance with BioNTech’s quality standards and global regulations. The Associate Director Safety Compliance is assigned to support the set-up and maintenance of safety compliance activities to ensure audit and inspection readiness.
**Your main responsibilities are:**
* Oversee safety compliance tracking and reporting
* Manage and update procedural documents related to safety processes, ensure all medical safety and pharmacovigilance activities are aligned with BioNTech’s quality standards, global regulations, and ethical requirements
* Perform process gap assessment as required and implement risk registers
* Support safety compliance and inspection readiness activities
* Active involvement in the preparation, conduct and follow-up of GxP regulatory inspections and audits impacting MSPv
* Conduct of MSPv focused mock inspections and lessons learned sessions as required from audit and inspection preparation perspective
* Process and document of non-conformities and CAPAs for the MSPv department
* Overall monitoring, tracking and analysis of deviation and CAPAs
* Contact person within the MSPv department for the relevant Veeva module for issue management
* Support BioNTech's Regulatory Intelligence activities and oversee PV Intelligence to develop, implement and continuously improve procedural documents and processes.
**What you have to offer.**
* Advanced degree in life sciences / healthcare (or clinically relevant degree)
* Expert knowledge of global pharmacovigilance regulations and processes, strong understanding of ICH, GVP/GCP modules as well as EU- and US- legislations
* At least 5 years of experience in Pharmacovigilance and/or Quality Assurance in biotech or pharmaceutical industry
* Experience with GxP audits and inspections and deviation and CAPA management
* Expertise in authoring procedural documents
* Proactive, solution-oriented with a collaborative mindset
* Ability to work effectively in global, cross-functional teams
* Good communication skills; is able to express complex matters in concise, clear language
* Fluency in written and spoken English
* Ability to accept shared responsibility with other team members to achieve results
**Your Benefits:**
It's our priority to support you:
* Your flexibility: flexible hours | vacation account
* Your growth: Digital Learning | Performance & talent development | leadership development | Apprenticeships | LinkedIn Learning
* Your value: Your voice at the table | Culture on an equal footing | Opportunities to shape & impact | Support for your full potential
* Your health and lifestyle: Company bike
* Your mobility: Job ticket | Deutschlandticket
* Your life phases: Employer-funded pension | Childcare
**Inspired? Become part of #TeamBioNTech.**
**BioNTech, the story**
At BioNTech, we are more than just a biotechnology company – we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cutting-edge science into survival. Your contributions here have the potential to improve the health of people worldwide, especially by addressing diseases with high medical needs like cancer and various infectious diseases.
Experience a dynamic workplace that embraces diversity in all its forms. We foster innovation, encourage creativity, and develop business strategies driven by our shared passion for advancing medicine.
Working at BioNTech means striving to achieve medical breakthroughs while growing your career in a meaningful way.
BioNTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. BioNTech is committed to creating a diverse and inclusive work environment. We are proud to be an equal opportunity employer. The main thing is that you suit us, and we suit you!
**BioNTech - As unique as you**