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About this PV Quality Assurance Manager (m/f/d) role at Valneva

Valneva · Onsite · Vienna, Vienna, Austria

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

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.

  • Maintain and continuously improve the Pharmacovigilance (PV) Quality Management System in compliance with global regulations and internal standards
  • Provide QA support for operational PV activities, including document control, archiving, deviation management, and CAPA oversight
  • Coordinate and deliver PV trainings while managing PV-related documentation and SOPs
  • Plan and conduct internal PV audits as well as partner qualifications and audits to ensure regulatory and contractual compliance
  • Support PV inspections, PASS activities, and maintenance of the PSMF
  • Support the QPPV with PV operational matters
  • Act as a key contact for internal stakeholders, fostering collaboration and PV compliance across departments
  • Drive continuous improvement initiatives related to PV quality, processes, and compliance

Requirements

  • 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:

    • Work Life Balance: Flexitime & Compensation days
    • Financial perks: Performance-related bonus & Lunch vouchers
    • 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.

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How this Quality Assurance salary compares

This role pays $58,516/yr — below the typical range for Quality Assurance roles.

$61,623 median $107,350 $157,391

Typical range $78,260–$134,100/yr, from 295 comparable Quality Assurance listings on JobsRadar (pay annualized to USD). See Quality Assurance salary insights →

About Valneva

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.

We have a strong track record, having advanced multiple vaccines from early R&D to approvals, and currently market three proprietary travel vaccines, including the world’s first and only chikungunya vaccine, as well as certain third-party vaccines.

Revenues from our growing commercial business help fuel the continued advancement of our vaccine pipeline. This includes the only Lyme disease vaccine candidate in advanced clinical development, which is partnered with Pfizer, as well as vaccine candidates against the Zika virus and other global public health threats.

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