2334 Qa Manager jobs in Milpitas,CA

QA Specialist

CCIntegration

San Jose, CA 95193

TE Connectivity

Milpitas, CA 95035

Master's degree in mechanical engineering, electrical engineering, industrial engineering, or closely related field (or foreign equivalent).
Plus 3 years of experience in the job offered, or in a related occupation.
Requires 3 years of experience with the following: 1. Navigating ISO 9000, IATF 16949, ISO 13485, ISO 14971 and FDA manufacturing systems and regulations.
2. Supplier Management.
3. Quality engineering toolkit including advanced understanding and application of statistics, sampling plans, data analysis, non-conformance management, DOE (Design of Experiment), GR&R; (Gage Repeatability & Reproducibility), verification, validation, SPC, control plans, risk management, CAPA (Corrective and Preventive Action), root cause analysis and tools (to include fishbone/Ishikawa diagrams, 8D problem-solving process and DMAIC - Define, Measure, Analyze, Improve, Control).
4. Application of lean manufacturing and six sigma tools and processes.
5. Project Management (scope, resources, cost, risk and communication).
6. Transfer of manufacturing processes from small scale development to large scale commercial manufacturing.
7. Computer applications: Minitab, MS Office, MS Project and MS Visio.
Generally requires Bachelors degree in appropriate field with a minimum of 8 years of experience

AMAX

Fremont, CA 94539

Bachelor's degree in Engineering or related field
5-7 years of experience in quality management within hardware, electronics, or manufacturing environments
Strong knowledge of QMS (ISO 9001 or similar)
Experience with root cause methodologies (8D, 5 Whys, Fishbone)
Familiarity with manufacturing of servers, storage systems, or similar hardware

Adecco

Cupertino, CA 95014

Bachelor's degree or equivalent relevant experience
2–5 years of experience in medical device labeling or regulatory labeling support
Strong understanding of global medical device labeling regulations, including 21 CFR 801 and EU MDR
Knowledge of Quality Management Systems (QMS), including design control, document control, and regulatory approval processes
Excellent written and verbal communication skills
Strong interpersonal skills with experience working across multiple cross-functional teams
Highly organized with strong attention to detail and time management skills
Ability to work independently and manage multiple priorities
Technical writing experience preferred