PT. Beurer Indonesia Technology memberi kesempatan untuk bergabung bersama Quality Engineering di .
Deskripsi Pekerjaan
Responsibilities:
- Audit: Prepare requirement for external audit (ISO 9001, ISO 13485, CPAKB, FDA 21 CFR part 820), and follow up corrective and preventive action for any nonconformance founded during audit.
- Reporting: Preparing the quality report for all kind of defect raw material, components and final product including problem solving analysis for continues improvement by weekly and monthly.
- Customer Satisfaction: Provide quick response to customer complaints, resolve the issues quickly and effectively including follow-up to ensure customer satisfaction.
- Documentation: Maintain accuracy records of QMS, technical issue and reporting for quality product.
- Project Participation: Collaborate with cross functional teams on Quality project and continuous process improvement.
Qualifications:
- Bachelor’s/Diploma on Industrial Engineering/Electrical Engineering/Mechanical Engineering.
- Minimum above 3 years’ experience LEAN manufacturing.
- Able to operate Quality Management tools and methodologies.
- Familiar with continuous improvement/KAIZEN.
- Have experienced job with an international industry will be an advantage.
Skills:
- Proficiency with Microsoft Office.
- Have Lean Sigma Belt holder will an advantage.
- Have knowledge with ISO 9001, ISO 19011, GMP and 13485.
- Have experiences preparing manufacture to comply with CPAKB & FDA 21 CFR part 820 (medical devices) is a plus.
- Excellent presentation, problem-solving and communication.
- Good written and spoken English language.
