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Quality Engineer Job Purpose:    Quality Engineer to maintain ISO/TS 16949 Program and provide support for current and future growth initiatives - OE/OES and aftermarket business.  Assist Quality Manager in maintaining the Prestone Quality Management System (Specifications) and support continuous improvement initiatives at Prestone manufacturing plants and contract packager locations. Position Responsibilities:   Maintain TS-16949 Program which include the following: Conduct TS Internal Audits of ...

I have a position available as a Web Application Developer. It is a full time position located in Brewster, NY. Position Overview As a member of the Application Development and Support team, the person will be responsible for the development and support of web based and mobile applications. The role requires interaction and coordination with teams in different time zones. The individual needs to be self-motivated, flexible, and independent. The individual would also play a critical role in ...

Job Description QA Documentation Associate supports functional objectives of assigned unit or team by performing a variety of activities in support of the functional processes, programs and/or services. Responsibilities: • Working on advanced department projects • Compiling and analyzing data • Creating reports • Providing information regarding function specific policies and procedures for applied use by management • Tracking and control of processes, projects and activities. • Use of new ...

QUALITY ASSURANCE MANAGER NEEDED ASAP!!! (Nyack) QUALITY ASSURANCE MANAGER NEEDED ASAP! COMPETITIVE SALARY + BONUS & EXCELLENT BENEFITS!!~ Directs and manages all aspects and functional areas of the NY Site QA Department, ensuring compliance with all regulatory and cGMP requirements. Provides oversight of quality functions and makes quality related decisions in the following areas: compounding, packaging, inspection, product disposition. Directly responsible for the management of QA ...

    Responsibilities     *           Organize and manage teams of engineering personnel for the purpose of verifying and validating product designs according to FDA requirements and internal quality standards to meet project delivery commitments. *           Accountable for ensuring execution against project schedules and Testing and Validation (T&V) standards/processes *           Manage automated tools to support product development documentation and engineering process improvement *           ...

Job Ref: #1610 Location: Danbury CT Relocation: No Salary: High Salary Summary: We need someone from a medical device, medical equipment, avionics, robotics type background. Electric vehicle could be a fit for example. It needs to be electro mechanical type hard equipment. Need a strong test and validation person with project management and medical equipment or something else that is highly complex. Duties and Responsibilities: 1. ...

QA MANAGER - MUST HAVE LEAN/SIX SIGMA EXPERIENCE (ORANGEBURG AREA, NEW YORK) Directs and manages all aspects and functional areas of the NY Site QA Department, ensuring compliance with all regulatory and cGMP requirements. Provides oversight of quality functions and makes quality related decisions in the following areas: compounding, packaging, inspection, product disposition. Directly responsible for the management of QA inspectors and Documentation Review Group. Reviews and approves all ...

 Summary of Duties and Responsibilities       * Organize and manage teams of engineering personnel for the purpose of verifying and validating product designs according to FDA requirements and internal quality standards to meet project delivery commitments.   * Accountable for ensuring execution against project schedules and Testing and Validation (T&V) standards/processes   * Manage automated tools to support product development documentation and engineering process improvement   ...

Seeking at least 5 years directing and coordinating quality assurance activities for good clinical practices, coordinate and oversee inspections to ensure compliance to FDA regulations, IRB and IEC regulations and guidelines, site SOPs, protocols, and industry standards. Shall: *** Direct and coordinate GCP quality assurance activities. *** Author GCP documentation: protocols, case report forms, tables, listings, reports, and investigational brochures. *** Plan and execute document audits and ...

SENIOR TECHNICAL PROJECT MANAGER POSITION SUMMARY: The Senior Technical Project Manager is responsible for coordinating multi-site development activities through the company's Design Control and Idea to Market process. This includes aligning and setting the project scope and objectives with all relevant stakeholders. He or she is setting and holding the team accountable for deliverable timelines, meeting performance requirements, and achieving project and development cost objectives. Development ...