Quality Control Manager
vor 2 Wochen
Valneva is a leading specialty vaccine organization dedicated to the development, production, and commercialization of prophylactic vaccines targeting infectious diseases with significant unmet medical needs. Our expertise has enabled us to successfully bring to market three vaccines, including the pioneering chikungunya vaccine, while also advancing a diverse portfolio of vaccine candidates through clinical trials, including those for Lyme disease and Zika.
With a presence in multiple countries, including Austria, Canada, France, Sweden, and the United Kingdom, we are committed to enhancing global public health. Our diverse and inclusive workforce fosters a collaborative environment, making Valneva an exceptional place to work.
Key Responsibilities
- Develop, maintain, and continuously enhance the quality assurance management framework for all operations at Valneva Austria, ensuring compliance with established Quality Assurance policies aligned with current Good Practices (GxPs), relevant Health and Safety Regulations, and applicable legislation.
- Lead and support initiatives aimed at the global harmonization of quality systems.
- Oversee and assist in computerized system validation projects in accordance with GAMP5 guidelines.
- Manage responsibilities within Valneva's electronic Quality Management System, including the enhancement of existing modules and the implementation of new modules on a global scale.
- Guide and support digital transformation projects aimed at replacing paper-based systems and processes.
- Facilitate the transition of electronic Quality Systems to Cloud-based solutions, integrating with other systems to enable data sharing.
- Actively contribute to Quality Assurance activities related to the administration and training of Quality Systems.
Qualifications
- HTL, Bachelor’s or Master’s Degree, or equivalent in a relevant discipline (e.g., Biotechnology, Bioengineering, Chemistry, Molecular Biology, Biology).
- A minimum of 2-5 years of experience in a QA/QC/GxP regulated environment, preferably within the Biotechnology or Pharmaceutical sector.
- Strong understanding of GMP guidelines and familiarity with regulatory bodies.
- Experience with electronic Quality Management Systems and Computerized System Validation.
- Proficient in knowledge transfer (training), with effective presentation skills for diverse audiences.
- Ability to organize and prioritize tasks in a dynamic office environment, with experience in developing and adhering to Standard Operating Procedures (SOPs).
- Excellent computer proficiency, communication skills, and fluency in both German and English (spoken and written).
- Capable of working cross-functionally, independently, and collaboratively within a team.
- Proactive and solution-oriented mindset in a rapidly evolving environment.
- Detail-oriented with a quick understanding of complex concepts.
Benefits
- Open and appreciative company culture that encourages innovation and offers engaging assignments.
- International work environment with flat organizational structures.
- Strong team spirit within a highly motivated team.
- A comprehensive benefits package including flexible working hours, compensation days, performance-related bonuses, meal vouchers, childcare services, company events, access to myClubs, and full access to LinkedIn Learning.
In compliance with legal requirements, we disclose the minimum salary for this position, which is € ,- gross per year based on full-time employment. However, our salaries are competitive and aligned with your qualifications and experience.
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