QA Validation

Do you want to be part of a world wide organization recognized as World's Best Workplace with the mission of saving patients through advanced biotech technologies?Our client's products reach over 10 million patients worldwide, that is why we are supporting them in looking for a Quality (Validation) specialist. In this role, you are mainly responsible to provide QA oversight for validation of equipment and packaging qualification in multiple international projectsContract Length: 12 months (possibility of extension or permanent contract after)Payrate: Min Pay rate- € 24,11 & Max Pay rate- € 25,38 (around 4.170 - 4.376/month)Hybrid: 2-3 days in the officeResponsibility:Provide QA oversight for equipment and packaging validation, ensuring compliance with corporate and regulatory standards.Review and approve validation documentation and master data in the PASX electronic batch record system.Support quality investigations and testing strategies.Review and approve equipment changes and technical change controls.Act as QA SME for deviation records and change control assessments.QualificationsMBO or Bachelor’s degree in Life Sciences, Process Technology, or Engineering (or equivalent).Minimum 2 years of experience in pharmaceutical or medical device industry, with a focus on equipment and automation validation.Solid understanding of GMP, Annex 11, Part 11, and computer system compliance.Fluent in English.