Qualification & Validation Specialist
QbD Group team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD.
What do we expect from you as a Qualification and Validation Specialist?
Provide quality and validation oversight to ensure that validation, qualification and other life cycle activities are consistent with company validation policies, procedures and federal regulations;
Proceed according to the company's quality policy in all business activities;
Provide advice to improve the quality policies and validation procedures;
Provide coaching, training and guidance on validations;
Implement controls to ensure data integrity and traceability of Quality records;
You have an academic background related to areas such as pharmacy, chemistry, biology, engineering and related fields.
You have at least 2 years of experience in qualifications/validations within validation departments in the pharmaceutical sector,



medical devices, biotechnology...
You have an advanced level of English: you should be able to write technical documentation in English.
Spoken English will also be an advantage as you will be joining a multinational company.
You have user-level computer skills: word processing, spreadsheet and database.
You are able to adapt to high quality standards, data integrity, GMP.
can be recognized by the following qualities:
that will be tailored to individual needs, considering legal requirements and local laws and regulations.
knowledge-based company
, you're guaranteed to embark on a continuous journey of learning and development.
Be part of our integral success story.
award-winning company
ambitious and pioneering company
, Full-time
Consulting, Project Management, and Science
Pharmaceutical Manufacturing and Business Consulting and Services
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📌 Ingénieur Validation (H/F) (Barcelona)
🏢 QbD Group
📍 Barcelona