Engineer Ii, Quality Operations CRM
6 days ago
Engineer II, Quality Operations CRM
As one of the world´s leading manufacturers of cardio
- and endovascular medical devices, BIOTRONIK is headquartered in Berlin, Germany, and represented in over 100 countries by its global workforce. The work of our committed, highly specialized, exceptionally skilled employees results in crucial advancements in the world of cardiology and changes the lives of patients every day.
**Your Responsibilities**
- Assist Lead/Senior Quality Engineer in preparation and presentation of standard reports (Quality figures, trending and analysis results)
- Execution of root-cause analysis on non-conformities and to initiate preventive and corrective actions. Ensures that corrective measures meet acceptable reliability /quality standards and that documentation is compliant with requirements.
- Coordination and evaluation of analytical tests data
- Leading the coordination and investigation of Product Non Conformities with the usage of RCA tools
- Training of production personnel as trainer on inspection specifications in accordance to inspection specifications
- Plan, test and qualify quality-related software changes and updates.
- Implements methods and procedures for inspecting, testing and evaluating/verifying the quality characteristics of the products/processes.
- On-site supervision of first series for new and modified processes in collaboration with other supporting functions e.g Process engineers, MES team, and Risk Management group
- Implementation of opportunities for improvement in regulations and maintenance of inspection documents.
- Support product transfer activities as Quality function representative
- Creation of Inspection plan in SAP and leading the coordination and investigation of deviations with incoming materials.
- Supporting/Leading Continuous improvement (CI) projects.
- Act as Quality function representative in validation activities
**Y**
**our Profile**
- Diploma with at least 5 years experience/Degree in the field of mechanical, Electrical, Bioengineering discipline, Quality Certification or equivalent
- At least 3 years of experience in quality role in an regulated environment (eg: medical devices, component manufacturing, pharmaceutical industry) or prior work experience in a technical area with strong affinity for Quality Assurance
- Quality Inspections techniques Analysis
- Quality Inspections techniques and experiences in handling measuring instruments
- Experience in using Quality Tools
- Experience with SAP and MES preferred (Manufacturing Execution Systems))
- Comprehending Technical Drawings
- Experience in Cleaning and Hygiene Regulations
- Preferred ISO 13485 Internal auditor / knowledge in FDA will be an advantage
- Knowledge in process validation and computer system validation
- Continuous Improvement (CI) Project experience
- Project management/ transfer experience will be an advantage
**What we offer**
- being encouraged to think and act entrepreneurially.
- working in global teams and projects.
- developing yourself professionally.
Location: Singapore | Working hours: Full-Time
Job ID: 58088
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, genetic information, or any other characteristic protected by law.
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