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Date Posted: 2021-04-29 | Expires: 2021-05-29
Portuguese Quality Manager (Medical Devices) - POR
Job Description
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.
Requirements
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
Benefits
to be discussed
Skills
Class III Medical DevicesLanguage Requirements
EnglishEducation Degree
High SchoolVisa Support
No
Job Criteria
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