QUALITY MANAGER MEDICAL DEVICE

Amstelveen

Permanent

Toegevoegd op 15/07/2010

Over onze client
Wright Medical Technology, headquartered in the US, is a global orthopedic medical device company specializing in the design, manufacture, and marketing of reconstructive joint devices and biologics. Wright's product offerings include large joint implants for the hip and knee; extremity implants for the hand, elbow, shoulder, foot and ankle; and both synthetic and tissue-based bone graft substitute materials.

Wright Medical Technology EMEA (WMT-EMEA) is the European Management structure covering a number of Wright Medical operations and third party distributorships within Europe, the Middle East and Africa. In order to fulfill European Regulatory Requirements as the Authorized Representative for Wright Medical Technology, as well as providing for a consistent Group business practice, WMT-EMEA operates an EMEA-wide Quality Management System, based on ISO13485. The EU Quality Assurance Manager therefore has a number of responsibilities defined by the Quality Management System (QMS) as well as by constraints imposed by regulations pertaining to the medical devices and biologics marketed within the EMEA region. In addition to the current team, we are recruiting a Quality Assurance Manager.

Omschrijving
Ensuring the continued operation and development of the QMS
Training of EMEA Group managers on the content and significance of the QMS
Analyze data and identify trends to improve the quality system's overall compliance, effectiveness, and efficiency
Implementation of continuous improvement plans in order to effectively update the QMS
Conduct, support or review failures, complaint investigations and corrective/preventive actions
Auditing of Group Companies and third party distributors for compliance against the QMS
Liaising with Wright Medical Technology - US with regards to Quality matters and Company strategy

Gezocht profiel
Bachelors Degree in technical field, preferably Science or Engineering
Three to five years experience required in medical devices or related field
A working knowledge of Quality Management Systems such as ISO9000 and ISO13485.
Plan and manage departmental activities in accordance with agreed budgets and timescales
Ability to develop and implement new systems and system level changes in the organization
Direct and lead teams to complete cross-functional projects
Willing to travel extensively, good investigative and organizational skills
Excellent communication skills in English, other major European languages are an advantage
Eager, structured, creative in problem solving, with strong social skills

Arbeidsvoorwaarden
A competitive package, based on education and experience level.

Michael Page Contact
Solliciteer online via onderstaand formulier of neem voor meer informatie contact op met Tessa Kramer op +31 (0) 33 4221550 onder vermelding van het ref.nr. UPTK149508.

Een referentieonderzoek kan onderdeel zijn van deze procedure

Referentie : UPTK149508

• 
•