Nu pierdeți cele mai bune locuri de muncă!
Abonează-te și săptămânal iți vom trimite un email cu ultimele locuri de muncă disponibile. Introdu adresa ta de email mai jos
Făcând click pe buton de mai sus, sunt de acord cu Termenii și Condițiile și confirm că am citit Politica de confidențialitate HelpGoAbroad.
Postat pe: 2021-04-29 | Expiră pe: 2021-05-29
Portuguese Quality Manager (Medical Devices) - POR
Descrierea jobului
QUALITY MANAGER - MEDICAL DEVICE - PORTO
Our Client is a medical device manufacturing company for class I and II devices looking to hire a Quality Manager, Medical Device to add technical depth to their team. This position reports to the CFO/CEO and is a highly autonomous role. Our client is part of an International group, you will be working in a dynamic international environment.
Main Responsibilities:
Provide technical direction, support and guidance for projects, qualifications and validations.
Manage the activities and performance of direct staff; this includes hiring, training, developing, addressing performance issues and evaluating performance.
Ensure a state of inspection readiness and meet business objectives.
Interface with auditors from regulatory agencies and customers.
Develop action plans, initiate, and employ training/development programs and assignments to further enhance technical skills and overall competencies of staff members.
Our Client is a medical device manufacturing company for class I and II devices looking to hire a Quality Manager, Medical Device to add technical depth to their team. This position reports to the CFO/CEO and is a highly autonomous role. Our client is part of an International group, you will be working in a dynamic international environment.
Main Responsibilities:
Provide technical direction, support and guidance for projects, qualifications and validations.
Manage the activities and performance of direct staff; this includes hiring, training, developing, addressing performance issues and evaluating performance.
Ensure a state of inspection readiness and meet business objectives.
Interface with auditors from regulatory agencies and customers.
Develop action plans, initiate, and employ training/development programs and assignments to further enhance technical skills and overall competencies of staff members.
Cerințe
Your profile:
Bachelor’s in Science or Engineering
5+ years in quality engineering within ISO 13485 regulated environment (MDD & MDR)
3+ years of management experience
Experience working with the European Notified Bodies
Bachelor’s in Science or Engineering
5+ years in quality engineering within ISO 13485 regulated environment (MDD & MDR)
3+ years of management experience
Experience working with the European Notified Bodies
Beneficii
to be discussed
Abilități
Class III Medical DevicesCerințe lingvistice
EnglishGradul de educație
High SchoolSuport viză
Nu
Criterii job
Companiile vor aplica la tine
Completează-ți CV-ul și companiile vor putea să-ți trimită invitații să aplici la joburile lor și te vom notifica prin email .