PV Quality Assurance Manager (m/f/d)
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Before you apply
Salary€52k
LocationVienna, Vienna, Austria
Typefull-time
SeniorityMid
Experience2+ yrs
Department11238
Company size501–1,000 people
PostedOct 19, 2026 · 2w ago
Verified live13h ago
At a glanceSummarised by Seekless from the posting.
Completed education in Life Sciences (Bachelor's degree or higher)
At least 2 years experience in the pharmaceutical industry, preferably in a global role
Excellent verbal and written skills in German and English are mandatory
Strong communication skills with internal and external stakeholders
Highly organized, with the ability to manage priorities effectively in a fast-paced, dynamic environment
Proactive team player with a collaborative and solution-oriented mindset
Experience in medical writing is an asset
Benefits
Flexitime
Performance bonus
Lunch vouchers
Sports activities
About the company
We are a specialty vaccine company that develops, manufactures, and commercializes prophylactic vaccines for infectious diseases addressing unmet medical needs. We take a highly specialized and targeted approach, applying our deep expertise across multiple vaccine modalities, focused on providing either first-, best- or only-in-class vaccine solutions.
Responsibilities
About the role
The Pharmacovigilance Quality Assurance Manager is a strategic role that drives enhanced compliance throughout the PV domain to support the obligation of the Marketing Authorization Holders and appointed QPPV, to maintain and improve a Global PV system in accordance with international regulations and Valneva standards.
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Maintain and continuously improve the Pharmacovigilance (PV) Quality Management System in compliance with global regulations and internal standards
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Provide QA support for operational PV activities, including document control, archiving, deviation management, and CAPA oversight
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Coordinate and deliver PV trainings while managing PV-related documentation and SOPs
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Plan and conduct internal PV audits as well as partner qualifications and audits to ensure regulatory and contractual compliance
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Support PV inspections, PASS activities, and maintenance of the PSMF
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Support the QPPV with PV operational matters
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Act as a key contact for internal stakeholders, fostering collaboration and PV compliance across departments
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Drive continuous improvement initiatives related to PV quality, processes, and compliance
Requirements
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Completed education in Life Sciences (Bachelor’s degree, or higher)
•
At least 2 years experience in the pharmaceutical industry, preferably in a global role
•
Experience in medical writing is an asset
•
Excellent verbal and written skills in German and English are mandatory
•
Strong communication skills with internal and external stakeholders
•
Highly organized, with the ability to manage priorities effectively in a fast-paced, dynamic environment
•
Proactive team player with a collaborative and solution-oriented mindset
Benefits
Working with Valneva means being part of a global biotech company with a clear vision to make a meaningful impact in the world. At Valneva, you can expect a dynamic and innovative work environment characterized by an open, appreciative company culture and exciting, impactful assignments. Enjoy the benefits of flat hierarchies, an international atmosphere, and regular company events that foster collaboration and connection.
Additionally, we offer:
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Work Life Balance: Flexitime & Compensation days
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Financial perks: Performance-related bonus & Lunch vouchers
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Health & Wellbeing: Free access to sports and fitness activities via myClubs & Office Massages
Join us and shape the future of biotechnology!
Due to legal reasons we are obliged to disclose the minimum salary for this position, which is € 52.000 gross per year based on full-time employment. However our salaries are market oriented and in line with your qualifications and experience.