European MNC with manufacturing of medical parts
Location: Ang Mo Kio Area
5 day work week
- Collaborate with internal stakeholder and customers on inspection, testing, process capability support and inspection plans
- Own nonconformance issues raised and drive for disposition, investigation, CAPA and customer communication
- Lead in ERP and QMS System
- Coordinate internal and external audits with reference to ISO13485
- Communicate with customers on process changes
- Conduct training, demonstrated work experience and tracking and update training system
- Collate quality documentation in areas of failed processes, material returns, customer rejects and corrections action
- Ad-hoc assignment with Global Quality Team
Requirement
- Degree / Diploma in Engineering
- 6 years of working experience in a manufacturing plant with focus in QMS and quality audit function
- Familiar with ISO13485 and ISO9001 QMS
- ASQ certified Quality Engineer is preferred
- Documentation Control and proficient in problem solving tools Minitab, Geometric Dimensioning and Tolerancing, 7QC tools, 5Why, 8D and lean / six sigma
- Independent, team player and customer oriented
