.Quality Customer Project Expert (m/f/d) page is loadedQuality Customer Project Expert (m/f/d)Apply locations ES - Porriño time type Full time posted on Posted 30+ Days Ago job requisition id R56543Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.Here in Porrino (situated 20min from Vigo), we are looking for an experienced Quality Customer Projects Expert to join our ever expanding, highly successful team.You will be responsible for managing customer projects within Quality Unit (QU) area, Representing the Quality Unit in multi-disciplinary customer project teams ensuring that all the projects fulfills quality standards, adherence to timeline and scope and on time and in full deliverables during the project lifecycle and acting as a liaison between the customer and different departments within QU and other project ´s stakeholders, coordinating technical SMEs throughout all stages of the projects balancing customer needs and business goals.Key responsibilities:- Quality representative in the different multidisciplinary teams for customer projects being responsible for the actions follow-up and any deliverable for the project team.- Collaborate to ensure that tasks are prioritized, completed on time, and communicated in an effective and timely manner.- Create, review and approval of process documentation as required (i.E. specifications, sampling plans).- Creation, review and approval (as applicable) of Stability Protocols and Reports.- APR (annual product review) management.- Management of complaints and product recall- Lot Disposition- Monitoring of the final product from the quality perspective (ISAs/OOC/OOT management as applicable) and Continued Process Verification (CVP) contribution.- Lead/collaborate with Test method transfer managing master protocol and report.- In close collaboration with the program manager ensure that project amendments are accurate and workload estimation is correctly assessed.- Ensure regulatory and customer inspection readiness and represent the department and participate in audits/inspections as required.Key requirements:- Bachelor of Science (Pharmacy, Chemistry, Biology, Biotechnology, Biochemistry...Etc) or proven experience in Quality Field- Several years (at least 5 years) of work experience in the pharmaceutical industry (preferably within Quality Assurance) experience in a GMP environment and Quality systems.- Experience in the communication with external clients and projects management- Statistical knowledge (e.G