ISO Jobs in Windsor

This position will provide technical support to silicone coating line for quality issues/concerns encountered on qualified grades troubleshooting/support for new products/grades oversee quality technicians as well as maintain corporate ISO program. Industry: Paper and Film Produc More...

Specialized Requirements Experience with data retrieval (SQL) scripting languages (Python Go Perl Linux) analysis and dashboarding Experience with security compliance frameworks controls and best practices: AICPA Trust Principles (SSAE 16 SOC 2 and 3) ISO 27000 Series CSA CCM P More...

Hello Trust this email finds you in good cheer!! Im Rupender from SiriInfo. I have an opportunity with me you might be interested please review the Job specifications below and let me know if you may be interested in this opening or may refer someone to me for this. For you referen More...

Quality Management ISO 13485 Medical Device Regulatory Standards Quality Compliance CAPA / NC Windchill PLM system Quality Engineer A minimum with 5 years of related experience Quality Management in Medical Device Industry Knowledge of Medical procedure and corresponding Medical Equi More...

Our client a successful manufacturer in the Indianapolis area (relocation will be provided) is seeking a Plastics Manufacturing Engineer who will be responsible for designing developing and optimizing plastic manufacturing processes and systems to ensure efficient production pro More...

Quality Engineer5 years of work experience in the Medical Device industry in Quality role Understanding on Medical Device Quality and Compliance Knowledge on ISO 13485: 2019 and 21 CR 820 Experience in Complaints Handling Post Market Surveillance Knowledge on Medical D More...

The Manufacturing Supervisor is responsible for overseeing and facilitating daily manufacturing activities ensuring the safe and efficient production of components and/or finished products. They provide leadership and motivation to technical and hourly associates focusing on achieving More...

Job Description: 5 years experience in Occupant Protection CAE working for an Automotive OEM or equivalent experience Execute simulations to evaluate full vehicle and sled level Occupant protection performance for frontal side and rear impact Capable of integrating various restraint More...

Job Description: JOB SUMMARYCoordinate validation activities for the clientPerform evaluate and analyze validation protocols and associated data for compliance with FDAand ISO guidelines.Assist with executing to the Validation Master Plan for the plant site.Identify schedule and perfo More...

This is a highlevel managerial position where the employee is responsible for organizing directing controlling evaluating and implementing through a functional management team the production operations of highquality mining accessories railroad snowplow System 2000 Boards custom machi More...

Required Qualifications 7 to 10 years of combined information security risk compliance and governance experience Knowledge of and experience in utilizing various methodologies and frameworks (NIST COBIT COSO ITIL ISO 27001/27002 and 27018) Strong knowledge and understanding of SOX an More...

Job description: Qualifications: Bachelors degree in computer science Information Technology or related field. Extensive experience in L2/L3 production support preferably within the Payment Domain. Strong understanding of payment processing systems and associated technologies. Pro More...

Fremont CA Contract Duration: 3036 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a QC Associate III in the Fremont CA area. Performs tasks and activities related to supplier/material qualifications and supplier change notifications (e.g. review of v More...

Our client a growing Cell Therapy company is looking for a Manufacturing Planning Supervisor. The job responsibilities are as follows: 1. Production and Warehouse Oversight: Manage and oversee both production and warehouse activities to ensure seamless operations. Manufactu More...

Job Description: JOB SUMMARYCoordinate validation activities for the clientPerform evaluate and analyze validation protocols and associated data for compliance with FDAand ISO guidelines.Assist with executing to the Validation Master Plan for the plant site.Identify schedule and perfo More...

This is a great opportunity in a beautiful upscale town outside of Springfield MA near Vermont and New Hampshire (no income tax) with nearby colleges. This 200person site produces a variety of extruded polymer films for medical devices electronic devices passport covers and use in the More...

Role : QA Engineer Location: Irvine CA (Onsite) Duration: Contract A minimum of 7 years of experience in Quality Engineering or Quality Assurance including data analysis risk assessment and risk mitigation is required. Working experience in good manufacturing practice regulated e More...

Project Manager Medical Device Experience Irvine CA or Danvers MA Onsite Hire Fulltime Hire Job Skills and Responsibilities: Project Management Professional (PMP) certification is required Must possess knowledge of theoretical and practical fundamentals and experimental en More...

Job Description: Position Summary:The Technical Writer II is responsible for supporting the Quality Assurance and Regulatory Affairs teams by creating revising and maintaining documentation related to IVDR submissions. This role works crossfunctionally with Manufacturing Operations an More...

Responsibilities/Duties: Perform all duties in accordance with requirements of ISO 9001:2015 and AS9100:2016 Rev. D Quality Management Systems. Accurately produce and diligently maintain all required quality inspection documentation on a daily basis. Read and interpret blueprints aer More...