Senior Quality Engineer to Cochlear

Cochlear Bone Anchored Solutions AB is committed to hearing and facial rehabilitation.We are a rapidly expanding medical device company focusing on bone anchored solutions based around the principle of osseointegration.On our website you can find out more about how our product systems Baha® and VistafixT is improving the quality of life for people all over the world.Entific was created in 1999 as a spin off of the Swedish oral implant group, Nobel Biocare.Since its inception, Entific has shown healthy growth especially in the hearing rehabilitation market.Dynamic product development, well adapted products, a committed team who understand the medical environment and high patient satisfaction mean this success looks set to continue.New indications in hearing rehabilitation will further broaden in future. In March 2005 Entific Medical Systems AB was acquired by Cochlear Ltd of Australia, the world leader in cochlear implants.This has contributed to a highly enlarged sales organisation and will further strengthen the organisation.Entific has become Cochlear Bone Anchored Solutions AB in October 2006.Read more on website: www.cochlear.com The turnover for the total Cochlear group is 2,4 Billion SEK and the average number of employees are 1100. We now need to further strengthen the Quality & Regulatory team The main task as Senior Quality Engineer at Cochlear BAS will be the responsibility for the company's system for internal audits, including planning, implementation and follow up on non-conformities and CAPA s, thus ensuring that Cochlear continues to produce reliable and compliant products that satisfy customer requirements. Responsibilities .Responsible for planning and implementation of internal audits .Active participation in the making and implementation of quality procedures .Provide advice and training on quality system requirements .Responsible for the companies system for Corrective and Preventive Action .Act as project manager for various quality system related projects Below we have listed Previous Knowledge and Experience that we believe is a suitable background for a successful candidate, together with important Personal Skills : Knowledge and Experience .Experience of planning of and implementing internal audits .Knowledge of quality systems from medical devices (ISO 13485 / FDA QSR) .Experience from LEAN manufacturing is an advantage .Experience from automated systems for document handling .Report writing and documentation skills .Excellent English language skills together with MS Word and Excel Personal skills .High communication capabilities .Concern for order & quality .Relationship building .Training capabilities We cooperate with Proffice Life Science in this recruitment process.Apply before 10th of January