Description
Medical Devices Quality EngineerLocation: London
Rate: £32.00 - £38.00
Job Type: Contract 6 Months
Our client, a global pharmaceutical company, seeks a Medical Devices Quality Engineer to join their growing team to produce and maintain quality throughout the development and implementation of new products.
As a Quality Engineer, you will be responsible for: .Producing & maintaining quality process specifications as required during the development & implementation of new products (Incl. on-site production & purchased resale goods). .Program coordinate measuring machines (CMM) and carrying out program verification activities. .Developing & improving inspection strategies for manufactured products. .Ensuring maintenance of quality assurance sections of device history files (DHR) and device master records (DMR) as directed by document control. .Assisting & leading in the collation & execution of validation protocols for new products / processes & software, including re-validation as required due to engineering change, deviation analysis or upgrade in systems & materials. .Managing QA change control. .Coordinating product / technology transfer between facilities including utilising DFMEA / PFMEA and other QA risk analysis techniques in order to limit potential risk. .Producing automated verification solutions. .Introduction & correct use of statistical QA methods into the production environment and providing technical resource for production teams on relevant IQ/OQ/PQ protocol issues. .Supporting adequate product specific microbial assurance activities via appropriate liaison with Microbiologist and product packaging group. .Ensuring compliance with all Documented Quality system, FDA QSR's and ISO 9001 requirements during day to day and assigned audit / CAPA activities. As a Quality Engineer, you will have the following qualifications, skill sets & experience: - A qualification or apprenticeship in an Engineering discipline (or equivalent) or equivalent experience. - Demonstrated experience in a Quality (QA) Engineer function including an understanding of quality systems and techniques such as SPC, AQL, FMEA,ISO9001, FDA QSR's and CGMP's. - CMM operating and programming experience. Gauge design and a good understanding of geometric tolerancing would be advantageous but not essential.
This is a great opportunity for a contractor to add a house hold name to their C.V, and to work within one of the most talented teams within the Medical Devices industry.
To apply please respond with an up to date C.V for consideration.
If you have any quires please call Oliver Percy on