Cefar-Compex Medical AB seeks a Quality Engineer

Cefar-Compex Medical AB is a growing medical-technology group with a leading position within the field of electrical nerve- and muscle stimulation.Cefar-Compex is owned by DJO and is represented in more than 30 different countries, with offices in Sweden, Norway, Switzerland, France and Spain.For more information: www.cefar.se Cefar-Compex Medical AB is currently seeking a Quality engineer that has a large interest to drive and development Cefar's quality management system and processes.Due to the fact that Cefar's products are sold globally, including the USA, Cefar must fulfil FDA global standards and strive after continuous improvement in their daily processes.Opportunities are abundant for a person who seeks a challenging and international working environment within the medical industry.Main responsibilities: . Maintain and support Cefar's quality system to ensure it meets global quality standards . Contribute and develop new and improved routines and procedures in Cefar's documentation process that support the organisation in delivering in a simple and effective manner .Responsible for reporting quality issues directly to Quality Director .Responsible for planning and implementation of internal and external audits as well as supplier audits, strong focus on follow-up of these processes .Registration of products within the EU and USA.Support distributors with registration in other countries . Analysis of customer input and complaints, report handling as well as feedback, communication and coordination with respective departments and suppliers to ensure correct follow-up procedures . General development and coordination within all issues of quality assurance You will report directly to the Director of Quality and Regulatory Affairs.The position is a one year temporary position during the current Quality engineer's maternity leave, and while one can not be promised permanent employment after the one year, there are many opportunities for the right person.Background You have a BSc or engineering degree with 3-5 years experience in a quality management environment or relevant area preferably within the medicine industry.Experience with quality systems and processes such as ISO 9001, ISO 13485 are an asset.You have strong skills in both oral and written English as well as strong computer/system knowledge, preferably knowledge of electronic documentation systems.You are structured, communicative and analytical.You thrive in a challenging and results oriented working environment and have the ability to carry out projects simultaneously.You are a strong collaborator when working with teams, as well as an effective team player and are extremely service minded in your way of working. To apply for the position, click the link below, fill in your contact details and attach your letter of intent together with your CV, written in English or Swedish.