Join to apply for theQualification & Validation Specialistrole atQbD GroupQbD 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 adviceto 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.Atrue QbD'ercan be recognized by the following qualities:QbD Group offers you anattractive and competitive salary package, that will be tailored to individual needs, considering legal requirements and local laws and regulations.Be part of our integral success story.
Seniority levelAssociateEmployment typeFull-timeJob functionConsulting, Project Management, and ScienceIndustriesPharmaceutical Manufacturing and Business Consulting and Services#J-*-Ljbffr

📌 Ingénieur Validation (España)
🏢 QbD Group
📍 España