At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self:Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self:Care for Everyone, we are the people behind the brands you trust. We are Opill(R), Compeed(R), Solpadeine(R), NiQuitin(R), ACO(R), and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging. Join us on our One Perrigo journey as we evolve to win in self:care. Description Overview Scope of the Role - Represent QA in computer system validation projects including change controls, deviations and periodic reviews and Data integrity for CSCI - Provide support with guidelines and regulations such as GAMP 5, EU GMP Annex 11, and FDA CFR Part 11 - Act according to the Quality Assurance (QA) vision, strategy and standards for the integrated Perrigo CSCI group - Keep going awareness of new and developing regulations (different ISO regulations, GMP, GDP, MDR, MDD). - Support in the maintenance of Quality Systems, including electronical systems (Trackwise, LMS,...). - Provide QA training to the entire group (European branch of the Perrigo Company) regarding computer system validation and Data Integrity and evaluate training effectiveness, including the creation of powerpoint presentations, online recorded trainings, etc. - Ensure adherence to critical procedures and compliance to requirements for record retention. - Be part of third:party qualification and regular third:party auditing for all topics related to Computer System Validation and Data integrity. - Assist in performing internal QA audits. - Support in the maintenance of the Quality Management System by creating and updating Standard Operating Procedures, Best Practices and Working Instructions. related to Computer Systems and Data Integrity - Provide support in establishing and maintaining the ISO 9001 and ISO 13485 Quality Management System related to Computer Systems and Data Integrity. - Identify gaps and areas for improvement in QA processes related to Computer system and handling and lead remedial actions and initiatives. Experience Required - Bachelor degree in IT, engineering, biochemistry, chemistry or equivalent through experience. - You are fluent in spoken and written English, other languages are a benefit. - At least 2:5 years relevant experience in Computer system validation in Pharmaceutical and/or Medical Devices industry - Deep knowledge of FDA regulations (especially CFR Part 11), EU GMP Annex 11 and GAMP 5. - Knowledge of the relevant European regulations for pharmaceutical products (GMP specifically Annex 11, GDP), Medical Devices (MDR, MDD, ISO13485, ISO14971), Food, Food Supplements (HACCP, ISO 22000) Cosmetics (ISO 22716) is an asset Benefits We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally. Find out more aboutTotal Rewardsat Perrigo. Hybrid Working Approach We love our offices and the setting they provide for in:person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles. We are proud to be included in the Forbes list of Americas Best Employers by State 2024. Find out morehere Applicants please note: to this position please click the APPLY button at the bottom of the application.(The