Specialist quality assurance qualification & validation (f/m/d)

Your responsibilities:Responsible, as QA representative in multidisciplinary teams, to oversee and review/approve qualification/validation documents and risk assessments for the following topics:Qualification of Equipment, Facilities, UtilitiesComputer System Validation (CSV)In this role the QA Specialist:leads the implementation of the qualification/validation strategysupports the transfer from project into commercial production phaseis the QA representative during qualification/validation workensures that the allocated quality-systems are compliant with regulatory expectationsestablishes and continuously improves quality procedures within the area of responsibilitycontinuously improves the allocated quality systemssupports changes and corrections for the area of responsibilityparticipates in audits and inspection within the area of responsibilityWhat you bring to the table:Master’s degree in Engineering, Biotechnology, or related field.Minimum of 5 years relevant experience in a Gx P regulated pharmaceutical/biotechnology industry.Minimum of 3 years validation and qualification experience requiredSolid computer skills including MS Office required.Analytical thinking and problem-solving attitudeMultilingual – at least German and English, written and spokenWe provide an opportunity to be a part of an international company that boasts exceptional technology and a determined team. Join our dedicated and agile IT team if you share our enthusiasm and have a desire to create an impact. You can expect a vibrant and adaptable work environment that supports the growth of your personal and academic skills. Additionally, we offer an extensive benefits package and a competitive compensation package.Caught your interest?We look forward to receiving your application directly on our recruiting portal: Init.aspx?cid=1576& Project Id=146796& Department Id=18964& Skip Advertisement=true