System One Litchfield, Connecticut, 06759 Position Summary: The Quality Manager is responsible for developing and implementing quality assurance policies and systems, monitoring quality assurance processes. The Quality Manager is responsible for ensuring that quality standards are met. The Quality Manager is responsible for monitoring the working conditions of the entire facility to ensure that all activity is compliant with local, states |
Joulé Fremont, California, 94538 Job Title: Quality Assurance Location: Fremont, CA Compensation: $20.00- $30.00 Type: Contract Join one of the world's leading medical technology companies. Alongside their customers around the world, they impact more than 150 million patients annually. Responsibilities Conducts routine and non-routine analysis, including but not limited to biochemical and chemical analysis, of raw materials, in-p |
Joulé Princeton, New Jersey, 08540 Job Title: Global QA Event/CAPA Coordinator Location: Princeton onsite candidate preferred, potential for remote Shift: M-F 8:30 AM – 4:30 PM Type: Contract (1 year) Pay Range: $45-$90/hour -depending upon experience This is an outstanding opportunity to work with a global household products company- making many different brands that everyone knows and loves. Must Haves/Requirements: Top 3-4 Skill |
Joulé Kutztown, Pennsylvania, 19530 Job Title: Quality Control Manager Location: Kutztown, PA Type: Direct Hire Schedule/Shift: Monday-Friday 6 AM to 2:30 PM Start: Immediate Responsibilities: Tests and inspects products at various stages of production process and compiles and evaluates statistical data to determine and maintain quality and reliability of products by performing the following duties. Interprets engineering drawings, |
Joulé Santa Clara, California, 95050 Our client is looking for Title: Biological Regulatory Quality Assurance Specialist III Candidates should bring- Bachelors' degree in Biological Sciences, Engineering or related field, or equivalent combination of education and work experience. * 2-4 years related experience in relevant medical diagnostic/device industry, including 1-2 years of direct Quality operations. Experience focused on qual |