Quality Manager (Postmarket)

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Quality Manager - Post Market SurveillanceAre you an experienced Quality Professional looking to take the next step in your career? Would you like to work with a family owned Medical Device company, who are known for being one of the top employers locally, and prioritising the wellbeing and work life balance of their employees?I am currently recruiting for a Quality Manager to join one of my key clients in Limerick on a permanent basis, leading their Post Market Surveillance division. The Role:You will manage the Quality Engineering Post Market Surveillance group, which is comprised of the Regulatory Communications and Complaints Investigation (including post market Quality Engineering) teams.You will be responsible for the day to day performance management of team members, including agreeing objectives, generating training plans and providing coaching, performance appraisals, dealing with performance related issues and allocation of tasks according to workload.The Quality Manager in this role will have responsibility for implementing requirements in accordance with ISO13485, MDD 93/42/EEC, EU Medical Device Regulation 2017/745 and FDA QSP 21CFR Part 820 as required, and actively pursuing ways in which to improve the function of the Quality Engineering PMS Department.You will also act as delegate for the Senior Quality Engineering manager in their absence. The Package:You will receive a very competitive salary, and comprehensive benefits package, including annual bonus up to 12%, full family health insurance, pension, educational assistance, onsite gym and parking, subsidised canteen, sports and social clubs etc.This role also allows for very flexible hybrid working, requiring a minimum of one day per week onsite.The Company:You will be joining a leading family owned, global Medical Device company, who are well known to be one of the top employers in Limerick.They specialise in the manufacture of devices for minimally invasive procedures, working across a rang of clinical areas including Vascular Surgery, Urology, Oncology, General Surgery, etc. Requirements:You will be a Quality Engineering professional with at least 7 years of experience in an ISO 13485 regulated manufacturing environment, with proven team leadership experience and a proven history of working with ISO13485, ISO14971, the Medical Device Directive, EU Medical Device Regulation 2017/745 and the FDA QSR.A minimum of a Level 7 qualification in Science, Engineering, Quality or a related discipline is also essential.If you would like some more information on this role, please apply here, or contact me directly on 01 888 3478. To find out more about Real please visit www.realstaffing.comReal Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales