Quality Engineering Manager
- Recruiter
- Anonymous
- Location
- Essex
- Salary
- Competitive
- Posted
- 14 Apr 2018
- Closes
- 09 May 2018
- Sectors
- Engineering
- Contract Type
- Permanent
- Hours
- Full Time
Your Responsibilities:
• Supervision and management of 7 direct reports and a team of Quality Engineers, Technicians and Quality Controllers
• Ensures quality assurance procedures, processes, practices and controls are properly developed, implemented and maintained
• Ensures that all products represent the maximum quality and reliability attainable.
• Routinely provides guidance and leadership to engineers, inspectors and/or technicians for the duration of a project assignment
• Active participation in ensuring product issues are promptly investigated and adequate corrective/preventive action implemented e.g. customer complaints, out of specification components, etc.
• Resource planning
• Generate control plans
• Review and approval of technical documents
• Problem solving
• Supply chain development
• Project management
• Drive regulatory compliance strategies
• Develop and ensure quality, regulatory and management reports are accurate and delivered within agreed timelines.
Your Qualifications:
• Degree, or equivalent, in an Engineering or Life-Sciences Discipline.
• Five years experience in a Quality Systems and/or Engineering role within an Electro-Mechanical or Electronics or Sterile Medical Devices Manufacturing environment.
• Experience in a Medical Device facility and knowledge of FDA Quality System Regulations (21 CFR 820), EU MDD, JPAL, ISO13485 and ISO9001 highly desired
• Proven track record in a supervisory role.
Your Competencies:
The interview will be competence based and the following competencies will be assessed:
• Communication
• Continuous improvement
• Leadership & responding to change
• Teamworking
• Supervision and management of 7 direct reports and a team of Quality Engineers, Technicians and Quality Controllers
• Ensures quality assurance procedures, processes, practices and controls are properly developed, implemented and maintained
• Ensures that all products represent the maximum quality and reliability attainable.
• Routinely provides guidance and leadership to engineers, inspectors and/or technicians for the duration of a project assignment
• Active participation in ensuring product issues are promptly investigated and adequate corrective/preventive action implemented e.g. customer complaints, out of specification components, etc.
• Resource planning
• Generate control plans
• Review and approval of technical documents
• Problem solving
• Supply chain development
• Project management
• Drive regulatory compliance strategies
• Develop and ensure quality, regulatory and management reports are accurate and delivered within agreed timelines.
Your Qualifications:
• Degree, or equivalent, in an Engineering or Life-Sciences Discipline.
• Five years experience in a Quality Systems and/or Engineering role within an Electro-Mechanical or Electronics or Sterile Medical Devices Manufacturing environment.
• Experience in a Medical Device facility and knowledge of FDA Quality System Regulations (21 CFR 820), EU MDD, JPAL, ISO13485 and ISO9001 highly desired
• Proven track record in a supervisory role.
Your Competencies:
The interview will be competence based and the following competencies will be assessed:
• Communication
• Continuous improvement
• Leadership & responding to change
• Teamworking