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Resumes 11 - 20 of 743 |
Santa Clara, CA
... the Regulatory team with preparation and assembling 510(K) and FDA Response Letters ●Received SAP training to submit POs for upcoming Notifying Bodies (NB) audits and procure the goods and services for the Quality Department Loral Space System, Mt. ...
- Mar 30
Pleasanton, CA, 94566
... ***-**** ad4jpj@r.postjobfree.com Experienced hands-on professional with specialties in high tech,bio-technology and bio-medical devices, knowledgeable in various logistics, export and manufacturing processes of medical devices, FDA,GMP,SOP's & ISO. ...
- Mar 24
Menlo Park, CA
... Designed test benches for functional simulation and completed documents used for FDA clearance submission Hardware Developer September 2015 – February 2016 Xilinx IP configuration & top-level integration 1 • AXI-DMA&-GPIO data transfer • Async. ...
- Mar 22
San Jose, CA
... •Support for resolution of FDA audit comment concerning supporting documentation for transporting of materials. •Write and execute shipping test plan for CDMO product. Baxter Healthcare & Lonza – Hayward, CA 05/08-07/19 Validation Engineering II ...
- Mar 19
Milpitas, CA
... • Experimented and contributed with writing a document on biomedical product requirement specification in accordance with FDA regulations, standards, and the Code of Federal Regulations (CFR). • Evaluated and analyzed information obtained from FDA ...
- Mar 17
Hayward, CA
... Department of Ag) SSOP (Standard Sanitation Operating Procedures) HACCP (Hazardous Analysis Critical Control Points) FDA (Food & Drug Administration) GMP (Good Manufacturing Practices) all safety policies and procedures and any other established ...
- Mar 16
Pleasanton, CA
... Worked closely with the Quality and Regulatory team, during the FDA audit. Monitored and maintained Help Desk tickets in the Remedy system. Imaged and deployed refurbished PC and mobile device hardware Setting up workstations Manage MS TEAMS ...
- Mar 13
Sunnyvale, CA
... Audio, video, digital conferencing, networks field system engineering Automotive safety and reliability standards, ISO 26262, FDA, IEC 61508 Creative thinking, agile and lean mindset, elegant works, fast learner, efficient communication and teamwork ...
- Mar 10
Redwood City, CA
... Managed developers around the globe to design, develop and deliver new software platforms following FDA guidelines. Led re-branding of department. Developed roadmaps and coordinated development activities for multiple GxP systems, (Quality Assurance ...
- Mar 07
San Bruno, CA, 94066
... South San Francisco, CA Labeling and Compliance Assistant in Regulatory Affairs, dealing directly with the FDA, JAMA, and the New England Medical Journal; and assisted with the Product Review Committee. Patent Litigation for the Legal Department: ...
- Mar 02