ISO Jobs in Hartford

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...

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...

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: 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...

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...

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...

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...

Job: Application Developer 4 Location : Remote or Boise Idaho Duration : Long Term Contract Candidate must pass standard contractual requirements (as listed on the Compliance tab) as well as the ILETS Fingerprinting/Background Check to be able to begin work. Once contractor is se More...

Please send me a word copy of your resume and your contact information if you are interested in below mentioned opportunity. Lab Technician IV St. Joseph MI 12months contract on W2 US Citizenship or Permanent Resident is required Must Have Skills Computer Skills: Prefer 2 More...

For further inquiries regarding the following opportunity please contact one of our Talent Specialists Sivanesan at Divya at Rashi at Title: Systems Engineer 2 (EARS)REMOTE Location: Remote (Candidate needs to be West Coast) Duration: 1.5 Years Job Summary: We are seeking a high More...