Quality & Documentation Specialist

**Aehr Test Systems** (NASDAQ: AEHR) is a market leader in the Semiconductor Capital Equipment Industry, providing advanced solutions for semiconductor Burn-In and Test for EV market. Our innovative single touchdown full wafer burn-in and massively parallel test systems are revolutionizing the power semiconductor industry. Come join our team! We are seeking...

Labelling and Documentation Specialist - 12 month contract - Fremont, CAOpportunity with a leading Medical Device companyAs part of Sustaining R&D, the Lead Analyst, R&D Technical Writing is responsible for creating end-user regulatory complaint product labeling. The specialist contributes to new product development and design change (sustaining) activities...

Labelling and Documentation Specialist - 12 month contract - Fremont, CAOpportunity with a leading Medical Device companyAs part of Sustaining R&D, the Lead Analyst, R&D Technical Writing is responsible for creating end-user regulatory complaint product labeling. The specialist contributes to new product development and design change (sustaining) activities...

Job DescriptionJob DescriptionSalary: $105-$120KAehr Test Systems (NASDAQ: AEHR) is a market leader in the Semiconductor Capital Equipment Industry, providing advanced solutions for semiconductor Burn-In and Test for EV market. Our innovative single touchdown full wafer burn-in and massively parallel test systems are revolutionizing the power semiconductor...

Job Title: Documentation specialist III - AutoCADLocation: Fremont, CA (Remote)Duration: 6 monthsMust have skills:Expert knowledge in AutoCAD and designSite facility knowledgeExperience in GMP manufacturing facilitiesAn ability to read, understand and modify Engineering drawings, including P&ID’sWork hoursCollaborative work must be performed in Pacific...

Job Title: Documentation specialist III - AutoCADLocation: Fremont, CA (Remote)Duration: 6 monthsMust have skills:Expert knowledge in AutoCAD and designSite facility knowledgeExperience in GMP manufacturing facilitiesAn ability to read, understand and modify Engineering drawings, including P&ID’sWork hoursCollaborative work must be performed in Pacific...

Job DescriptionJob DescriptionFremont, CAContract Duration: 5-24 monthsRate: NegotiableResponsibilities:Excellent employment opportunity for a Documentation Specialist I in the Fremont, CA area. This position leads all paper/electronic batch record review that is related to manufacturing of drug substance in a multi-product facility. The position performs...

**Position Summary**: ECS is a Documentation and Change Order (ECR/ECO) specialist responsible for engineering change control process as part of PLM. Beyond generating and processing Change Orders, duties will include data mining, POC for change related escalations, managing trackers, inter department reports and CIP activities in a high pace...

Documentation Specialist III / AutoCADDuties:The US Biopharma E&T (Engineering & Technology) Department is seeking a service partner to support revisions to our Facility and Engineering Drawings and Documentation database.These drawings are very critical to the site for design and maintenance activities.The drawings are maintained electronically in our CAD...

Job DescriptionJob DescriptionJob Title: Documentation Specialist IIILocation: Fremont CA 94555Duration: 7 MonthsJob Description:1st Shift: Mon-Fri, 8AM-5PMDuties:    The US Biopharma E&T (Engineering & Technology) Department is seeking a service partner to support revisions to our Facility and Engineering Drawings and Documentation database. These...

Overview: Processes and reviews underwriting requirements by conducting customer interviews to gather non-medical and medical information. Works with some supervision but is empowered to approve applications and other decisions within the limits of authority level, and coordinates workflow of cases outside authority limits with Senior Case Specialist....

Documentation Specialist III Location: Fremont, CA/Remote Duration: 6+ Months The US Biopharma E&T (Engineering & Technology) Department is seeking a service partner to support revisions to our Facility and Engineering Drawings and Documentation database. These drawings are very critical to the site for design and maintenance activities. The drawings are...

Description We're looking for a Quality Systems Specialist , working in Pharmaceuticals and Medical Products industry in Fremont, CA 94555, Fremont, California, 94555, United States . Job description: Support in the implementation and maintenance of our Inspection Readiness Program. Support process improvement initiatives for inspection readiness program,...

Duties: The US Biopharma E&T (Engineering & Technology) Department is seeking a service partner to support revisions to our Facility and Engineering Drawings and Documentation database. These drawings are very critical to the site for design and maintenance activities. The drawings are maintained electronically in our CAD (Computer Aided Design) database....

Overview: Summary of Responsibilities: Scans and indexes paper documents into the imaging system to trigger workflows for further electronic processing throughout the organization. Prioritizes imaging functions to fulfill requests in a timely and quality manner. All documents are to be handled in accordance with departmental standards including established...

Scans and indexes paper documents into the imaging system to trigger workflows for further electronic processing throughout the organization. Prioritizes imaging functions to fulfill requests in a timely and quality manner. All documents are to be ha Specialist, Transaction, Processing, Insurance, Healthcare, Training

Job DescriptionJob DescriptionRoleAs a Quality Technician (also known as Quality Control Specialist, Quality Assurance Technician), you'll compile and evaluate statistical data to maintain product quality and reliability. You'll perform both destructive and nondestructive tests on materials, parts, or products at various stages of the production...

The Senior Technical Publications Specialist will be responsible for creating end-user regulatory complaint product labeling that will support the EU MDR product.Accepting no less than the absolute best, our Client has climbed to the top, gaining a reputation for both excellence and satisfaction. Working at this company will give you the opportunity to work...

The Senior Technical Publications Specialist will be responsible for creating end-user regulatory complaint product labeling that will support the EU MDR product.Accepting no less than the absolute best, our Client has climbed to the top, gaining a reputation for both excellence and satisfaction. Working at this company will give you the opportunity to work...

Duration : 06+ monthsDescription: The Manufacturing Quality Engineering Technician will support the Manufacturing Engineering Team and work cross-functionally with Vehicle Engineering, Corporate Quality and Supplier Quality within. The Technician will use their technical background to perform root cause analysis on vehicles, record their findings, and...