Senior Validation Consultant

QbD Group is a pioneering company in the life sciences industry, offering tailored solutions for companies active in Pharma, ATMP, and Medical Devices/IVD.

We are seeking a highly skilled Senior Validation Consultant to join our team. As a CSV Specialist, you will play a critical role in managing and overseeing project deliverables for cutting-edge applications, including Automated systems, Software as a Medical Device (SaMD), and Mobile apps.

• Prepare and design projects from scratch to implementation and follow-up.
• Provide full-cycle support to clients, ensuring successful project delivery.
• Contribute to the integration and implementation of our proprietary QbD quality management software at client sites.

To be successful in this role, you will need:

• A master's degree in a scientific or engineering field (e.g., bio-engineering, bioinformatics, industrial engineering, civil engineering, etc.).
• Some experience in the Life Sciences industry or with software-related projects.
• A strong affinity with IT, software, and systems.
• Knowledge of data integrity.
• Detail-oriented, eager to learn, and adaptable to new challenges.
• Strong technical and project management skills.

At QbD Group, we offer an attractive and competitive salary package, tailored to individual needs, considering legal requirements and local laws and regulations.

You can expect a salary range of $80,000 - $110,000 per year, depending on your experience and qualifications.

In addition to a comprehensive compensation package, you will have the opportunity to work with a dynamic team, contribute to the development of innovative solutions, and enjoy a joyful community where you can be yourself.