Venture , a public listed company in SGX, is a leading global provider of technology services, products and solutions with established capabilities spanning marketing research, design, research and development. Over the years, Venture has built know-how and intellectual property with expertise in several technology domains. These include life science & genomics, molecular diagnostics, medical devices and equipment, healthcare and wellness technology, lifestyle consumer technology, health improvement products, instrumentation, test and measurement technology, networking and communications, fintech, as well as computing, printing and imaging technology.
Headquartered in Singapore, the Group comprises over 30 companies with global clusters in Southeast Asia, Northeast Asia, America and Europe, and employs over 12,000 people globally.
At Venture, our people are our most valuable asset. We are committed to unifying culture, encouraging innovation, and harnessing the collective strengths and synergies of our human capital to deliver compelling differentiation, advancing Venture’s position as a leading global provider of technology solutions, products and services.
We’re looking to add a Quality Engineer in Milpitas, California. The position will be based in our office at Milpitas, California.
As a Quality Engineer, you will:
- Support ISO 9001:2015, AS9001D, ISO 13485:2016 internal audit and implementation.
- Ensure quality related deliverables are met as defined by the product development process and project plans.
- Provide Quality Engineering and Assurance Services and Technical Expertise to support product quality and overall system compliance.
- Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements.
- Work with Manufacturing and Process Engineering to ensure product quality.
- Work with Customer SQEs and other related engineering fields in the completion of Product Qualification Process (PQP) and Production Part Approval Process (PPAP).
- Coordinate and manage the Corrective and Preventive Action system (CAPA).
- Lead Root Cause Investigations efforts using common Root Cause Analysis Methodologies (5 Whys, Fishbone Ishikawa, Pareto Charts, etc.)
- Active involvement in maintaining, reviewing and reporting Quality Performance Data (KPIs) and opportunities for improvement for management review.
- Evaluate product and process changes to assure compliance with regulatory, corporate, customer, and 3rd party safety requirements (UL, Intertek, CCC, Etc.).
- Participate in MRB/CPI to engage with process and yield improvement
- Monitor RMA return rate and support FA / Process improvement
- Ensuring that the quality management system conforms to the requirements of International Standard.
- Ensuring that the integrity of the quality management system is maintained when changes to the quality management system are planned and implemented.
What skills and experiences are we looking for?
- Bachelor’s Degree in Technical Discipline (Engineering, Math, Science or Equivalent Experience)
- At least 5 years of experience in contract manufacturing in PCBA and Box Build Assembly.
- Extensive knowledge and certified internal auditor in ISO 9001:2015, ISO14001:2016, ISO13485:2016 and AS9100D
- Familiar with DOE, FMEA, PPAP, SPC, PQP, TQM, ISO, Six Sigma
- Knowledge of the basic QA functions i.e. IQA, FQA, MRP, RMA, FAI, QCC, CAPA, SCAR, etc.
- Strong analytical skill and hands-on problem solver with decision making background.
- Strong Knowledge in Microsoft Office (Word, Excel, PowerPoint, Access Database)
- Understand SMT processes and quality requirements
- Good communication and writing skills
- Strong knowledge of PCBA (SMT and PTH) Box-Build and repair (RMA) business a must.
- Must be familiar with medical products requirements.
- Knowledge in IPC, Bellcore, and JEDEC standards.
- Statistical Process Control and / or Six-Sigma capabilities.
- Must be able to work independently with minimum supervision.
- Experience in PFMEA and Process Control Plans
- Experience in Eight Disciplines (8D) Problem Solving Methodology
- IPC-A-610 & J-STD-001 CIS or CIT Certification
- ISO9001, ISO13485 and AS9100 Internal Auditor Certification