QA - QA Expert Systems & Compliance

Job TitlepQA - QA Expert Systems Compliance /pbrWegens grote belangstelling verzoeken wij u snel te solliciteren als u een goede match bent voor deze functie.brLocationpAmsterdam, NLD, 1105 BJ /pDate PostedpPosting Start Date: 6/16/26 /pJob DescriptionpApply for the role in Amsterdam: QA - QA Expert Systems Compliance (Focus: Qualification/Validation). The QA Expert Systems Compliance reviews qualification/validation documents and coordinates and conducts QA activities. /pJob ResponsibilitiesulliReviews and approves qualification and validation documents in order to prepare the final QA release of equipment, systems, processes and computer systems; /liliEnsures, in cooperation with the responsible employees that errors in the documentation are corrected; /liliParticipates as a QA delegate in multidisciplinary project groups for the purchase, qualification and (re)validation of equipment, systems, processes and computerized systems; /liliReviews protocols, reports, test documents and other relevant documents in order to facilitate the final QA release of equipment, systems, processes and computerized systems; /liliRegister, calculate, check and assess data as needed to review relevant documentation; /liliParticipates in research and corrective actions related to quality issues at the request of QA management; /liliCarries out spot audits and formulates the follow‑up in collaboration with the relevant departments; /liliParticipates in external GMP audits and inspections of supply companies, customers and government agencies; /liliInvestigates reported deviations after a quality issue within production or QC. Coordinates follow‑up; /liliAssists in the preparation of annual reports and provides statistical overviews of the release data for the actual release; /liliParticipates in special interdisciplinary task forces where QA input is desired; /liliSupports QA management with regard to all developments in the field of quality, GMP and legal guidelines and plays an important role in further and wider integration of quality in the company. /li /ulQualifications RequiredulliMinimum Bachelor degree in the orientation of Analytical Chemistry, (Micro)Biology, Biochemistry or Pharmaceutical Sciences; /liliA minimum of 3 years experience in the pharmaceutical industry in the field of equipment qualification and related topics; /liliAbility to work with tight deadlines and handle multiple tasks; /liliComputer fluency in MS Office, e.g. Word, Excel, PowerPoint. Knowledge of Veeva and SAP is a plus; /liliExperience with FDA compliance is a plus; /liliProfound knowledge of Dutch and English language, verbal and written; /liliYou reside in and are eligible to work in The Netherlands (valid work permit). /li /ulWhat do we offer?ulliEmployment: A challenging and international position in a professional and informal working environment; /liliCompensation: Attractive salary, holiday allowance, home‑office travel allowance, participation in the company's success, subsidized pension plan; /liliWork‑life balance: Flexible working hours (where possible), 30 days of vacation; /liliVersatile development opportunities: Support for professional development, access to online learning platform GoodHabitz. /li /ulpAs an international company, we welcome the diversity of people. We consciously promote equal opportunities and a diverse, inclusive culture in our teams – this is what makes us successful. xgiwjmb /ppWe look forward to receiving your application! /ppbReference Code: 31168 /b /pbr