Quality Manager


Premium Job From Real Staffing

Recruiter

Real Staffing

Listed on

3rd August 2021

Location

Shannon

Salary/Rate

£63252 - £81324

Type

Permanent

Start Date

ASAP

This job has now expired please search on the home page to find live IT Jobs.

Title: Quality Engineering ManagerLocation: Shannon, Co. ClareBenefits: Excellent salary, pension, healthcare and yearly bonus. Summary:Quality Engineering Manager is responsible for leading quality engineering function for manufacturing processes, materials and products at my clients Shannon facility. This role is completed with support from the Quality Systems and Supplier Quality functions. Responsibilities:Manage and lead the Quality Engineering function at Aerogen Shannon driving process continuous improvements and providing manufacturing support, this includes:Process/manufacturing data analysis, trending, and assisting yield reporting.Investigation root cause analysis of quality issues in manufacturing and managing quality related NC's and CAPA'sEstablish analysis techniques and other quality control tools such as SPC, Cpk, PpkLead the Materials Review Board (MRB) process.Champion continuous process improvement and, in conjunction with other functions, analyse feedback and identify and implement appropriate problem solving and statistical techniques to improve quality of manufactured product and overall effectiveness and efficiency of processesAppropriately train, develop and manage all of the resources within the Aerogen Shannon Quality team to ensure objectives are communicated and delivered within agreed requirementsEstablish inspection plans, frequencies and test methods for incoming material/partsOverall responsibility for GMP standards and compliance within manufacturing areaLead Master Validation Process Plans and Process ValidationsDrive risk management activities in manufacturing (Process FMECA)Manage process quality control system to ensure all manufactured product meets defined specifications prior to shipment.Manage assigned aspects of the quality system in compliance with ISO 13485:2016: FDA QSR, MDSAP requirementsConduct internal audits as defined by audit schedules and ensure ongoing high level of readiness for all external audits.Perform other assigned tasks and support all aspects of the Quality System as directed by the Senior QA/RA Director Education/Experience:Degree in Engineering, Technology or Science. A Post-graduate qualification in Quality Assurance is preferable although not mandatory.6-10 years Quality/Quality Engineering experience or a related role within the medical device industry Would you be interested in hearing more about this new opportunity? If you would like to apply or have any questions forward me an up to date CV or email me to set up a call. 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

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