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Quality Assurance Jobs in Coronado, California

678 jobs

NDT Inspector II/III Requirements: RT Level II certification required (RT, Radiographic, X-Ray) Digital x-ray experience highly preferred. UT, Ultrasonic Level II preferred Plusses: Certification in PT, MT, UT. Primary Responsibilities: Assures that material and parts are properly processed to the applicable NDT Method Specification. Reads and interprets indications and evaluates discontin...
NDT Inspector II/III Requirements: RT Level II certification required (RT, Radiographic, X-Ray) Digital x-ray experience highly preferred. Plusses: Certification in PT, MT, UT. Primary Responsibilities: Assures that material and parts are properly processed to the applicable NDT Method Specification. Reads and interprets indications and evaluates discontinuities referencing quality document...
Description There are 4 openings: one each in Melbourne, FL: Wichita, Kansas; Chicago, Illinois and Long Island, NY. The positions in Kansas, Illinois and NY will be telecommuting only. Plans, organizes, directs and reports on all supplier quality -related activities to assure fulfillment of contract /purchase order requirements. Assures that customer quality-imposed requirements are adhered to ...
RESPONSIBILITIES: - Perform HVAC, Electrical and general inspection for energy upgrades to Federal facilities. - Complete daily logs describing the work, crew size, conditions, and issues - Review work for compliance with submittals, plans and specifications, quality of materials and workmanship of installation - Coordinate with Construction Management team for utility shutdowns, after hours w...
Title: Software Quality Engineer Location: San Diego, CA (92121) Duration: 12+ Months The Software Quality Engineering department provides independent software verification and validation services to assure the quality of software products prior to manufacture and/or customer release. Department team members work as a team to assure quality compliance by following the business unit’s Standard O...
Amec Foster Wheeler (www.amecfw.com) designs, delivers and maintains strategic and complex assets for its customers across the global energy and related sectors. Employing around 40,000 people in more than 55 countries and with 2015 revenues of £5.5 billion, the company operates across the oil and gas industry – from production through to refining, processing and distribution of derivative produc...
SAP Specialist Discover the Difference You Can Make at Gate Gourmet Gate Gourmet, a gategroup company, is the world’s largest independent provider of catering and provisioning services for the airline industry. For the past 70 years, we have served over 250 carriers in more than 30 countries. Gate Gourmet combines culinary expertise with the highest standards of food safety and production to del...
Description The System Test Engineer synthesizes customer contractual needs and requirements into system test solutions that acknowledges technical, schedule and cost constraints. Develops and directs preparation and execution of comprehensive test plans, procedures and schedules for completing systems. Coordinates integrated testing activities. Reviews and evaluates test requirements to insure c...
Company Overview Western Environmental Consultants, Inc. (Western ECI) is a leading provider of vegetation and asset management consulting services to the utility industry. Successful professionals at Western ECI have come from a variety of backgrounds, including: forestry, arboriculture, natural resource management, biology, landscape maintenance, horticulture, nursery management, environmental ...
This position is responsible for the review of batch records. In addition, incumbent performs physical release of Final Product and maintains metrics for the review turnaround times. The position may have interactions with internal departments. The QA Associate performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting data and documentation re...
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Responsible for implementing, maintaining and monitoring the compliance and workplace environmental, health, and laboratory safety objectives for a highly technical research organization. Conduct compliance reviews, employee training, and maintain regulatory reporting. Interprets and adapts policies, procedures, and regulatory standards to ensure compliance with applicable regulations. Has a lead ...
Biotheranostics, Inc. Quality Assurance Specialist Reports To: Senior Director, Regulatory Affairs and Quality Systems Overview Responsible for managing the development, implementation and maintenance of Biotheranostics’ documentation systems in compliance with FDA’s QSR (21CFR820) and CLIA regulations (42CFR493).These systems include document and product change management, training programs ...
Position Description Purpose of position: HSE Program - develops/adopts and supports the implementation of all HSE policies and programs to enhance occupational health, environmental protection and workplace safety. Maintain ISO 14001 and 18001 Management System The Safety Manager is responsible for supporting the employer (e.g. Managing Director), his line management and the people accountabl...
Description: For those who want to invent the future of health care, here's your opportunity. We're going beyond basic care to health programs integrated across the entire continuum of care. Join us and help people live healthier lives while doing your life's best work.(sm) Primary Responsibilities Serve as an integral member of the administrative service organization’s leadership team Provide...
Description: For those who want to invent the future of health care, here's your opportunity. We're going beyond basic care to health programs integrated across the entire continuum of care. Join us and help people live healthier lives while doing your life's best work.(sm) Primary Responsibilities Manage day to day operations and Quality Improvement staff. Manage QI staff workloads to ensure c...
Position Overview: Drive all elements of software quality assurance support to manufacture a range of medical devices; including product development, manufacturing operations, information systems and quality systems activities. Ensure external and internal quality system requirements are adhered to throughout product and process lifecycles. Develop and implement software design plans, detailed d...
Summary: Able to work independently, with responsibility for documenting, and evaluating complaints for USA Medical Device Reports (MDRs), EU Vigilance/Incidence Reports, or EU Mandatory Problem Reports filings. Provide direction to junior staff regarding reportability. Complete MDR filings and FDA updates as necessary, including follow-up activities. Follow up with internal and external sources ...
Summary Works as part of the Regulatory Affairs department with direct responsibility for developing regulatory plans with high level of complexity. Plans and prepares documentation for international and domestic product registrations for new and modified products. Interacts with governmental regulatory agencies, other third party accrediting bodies, and US trade associations. Tasks and responsi...
Summary Works as part of the Regulatory Affairs department with direct responsibility for developing regulatory plans with high level of complexity. Plans and prepares documentation for international and domestic product registrations for new and modified products. Interacts with governmental regulatory agencies, other third party accrediting bodies, and US trade associations. Tasks and responsi...
Description Help the development, modification and application of the quality/engineering Design Assurance (DA) processes for the purpose of reducing and/or eliminating escapes or omissions linked to design and to ensure design integrity and robustness while maintaining efficiency. This role requires collaboration with engineering, manufacturing, program management and many other functions to ens...