QRC Specialist UKI

With a passion for lifeJoin our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers.  Are you looking for an inspiring career? You just found it.Location: Remote role with travelJob OverviewQRC Specialist provides support to the QRC Director UKI for maintaining and improving a compliant Quality Management System (ISO9001, ISO 13485), including audits, CAPAs, regulatory monitoring, product registrations, and ensuring adherence to quality and compliance targets.Job Responsibilities and Essential DutiesA list of the main responsibilities and percentage of time spent in each responsibility or group of responsibilities:Support in Maintaining and controlling a Quality Management System based on ISO9001, ISO 13485 and Global proceduresAssisting in the investigation of NC handling in various tracking systems and following up on the corrective actionsAssist in (FSCA) Field Safety Corrective Actions Support and/or performing internal and external audits and support the QMS Manager with the follow up of these auditsSupport on all related CAPA’s and non-conformitiesAssisting in monitoring and maintaining quality and compliance targetsPreparing and analysing information for the purpose of Management ReviewStay alert on all regulatory changes, analyze the changes, and communicate, implement the applicable requirementsSupport in ensuring products are registered with the authorities (MHRA) within the required deadlinesAssist in any Regulatory changes, analyse, communicate, anticipate and implement the applicable requirementsInteract with the Authorities to provide requested feedback.Support the sales organisation with the complaint handling, ensure that the SSU’s are recording the complaints through the associated tools, within the time limitsSupporting the implementation of Field actions and Quality HoldsSupport and organise trainings and awareness to the SSU’s in Regulatory Affairs, Post-Market Surveillance, QMS Collecting and monitoring KPIs across the Quality Management SystemMinimum RequirementsA degree is desirable but not essential.Experience working with Quality Management System requiredExperience in the medical device industry is desirableKnowledge of ISO 13485 / ISO 9001Knowledge of NC and CAPA process desirableExcellent language skills in English – verbal and writtenRequired Knowledge, Skills and AbilitiesGood knowledge of Microsoft packagesSharePoint, E-learning, TrackWise experience is desirableKnowledge in Medical device regulation (MDR, UKMDR), MDD and EUMDR is desirableAbility to work unsupervised / remotely Ability to work well with others across UK and Ireland and other global locationsAbout us  With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.