3 jobs found in Santa Clarita

Company Summary: At Arvato, we measure our success through the successes of our customers. Our DNA is built upon Customer Obsession, Ownership and Continuous Improvement (Hustle). We achieve our goals by means of experience, state-of-the-art technologies, creativity, passion and a commitment to quality, innovation and having fun Come and join our team today Position Summary: Arvato Supply Chain Solutions is hiring a Quality Assurance Automation Engineer. The Quality Assurance team is responsible for working with PO, developers and other QA engineers in an agile environment to ensure all quality aspects of our web applications with proper testing coverage and efficient testing solutions by on-time delivery and by adhering to development and quality standards. You will define automation test plans, test strategy, test scope and test scenarios based on requirements. General Roles and Responsibilities: The QA Automation Engineer is responsible for implementing and maintaining automated test scenarios and frameworks; support defect fix testing, including reporting, tracing and troubleshooting defects; perform automation code review and technical support to the development team; triage and troubleshoot on issues found during testing, deployment and releases; and report test results. Minimum requirements: BS in information technology, engineering or a related degree A minimum of5 years of experience is required in software testing and/or development, completing several major projects with multiple release cycles Preferred Skills and Experience: Solid experience working in Agile Solid experience with release management, SQL and test automation (e.g. Integration and UI) is required

To apply visit www.careersatfralock.com CMM Programmer Starting Salary - $20/HR DOE – Full Time Benefits Hours: 3:30PM-12AM Description Fralock is a well-established manufacturing company, based in the Santa Clarita Valley, that has a 50 year history of excellence. We are looking for people who exemplify strong work ethics, values, dedication and character with the ability to make independent, intelligent decisions. If you thrive in a fast paced environment, which is focused on exploring and developing the next generation technology while offering opportunities for advancement, apply today. We offer Paid Vacation/Sick/Holiday, 401K (after 6 months of employment), annual bonus program (conditions apply), Medical/Vision/Dental coverage growth opportunities, training assistance programs and many more EEO/AA EMPLOYER/VETS/DISABLED/RACE/ETHNICITY/GENDER/AGE If you are still reading… Check this out Culture Vision: Our results driven team strives to deliver extraordinary outcomes through our passionate commitment to each other, collaboration, courage and innovation Main Functions Program metrology equipment such as CMM, KEYENCE machine, and vision systems. Perform inspection per drawing requirements. This position requires access to information controlled under the International Traffic in Arms Regulations (ITAR) or the Export Administration Regulations (EAR), the successful candidate must be a "U.S. person" as defined in the ITAR and EAR (which generally means (i) be a citizen or national of the United States; or (ii) be a lawful permanent resident of the United States; or (iii) have been admitted to the United States as a refugee, or have been granted asylum, as specified under applicable law. Typical Duties • Program and operate the CMM • Follow procedures, work and inspection instructions in the job orders • Perform inspections using CMM, handheld instruments and templates • Collaborate with Production, Receiving Inspection, and Purchasing when parts are found out of tolerance • Document results of inspections using First Article Report AS9102, Fralock Dimensional Report, copies of CMM report or written results in the job order • Issue Certificates of Conformance (COC) • Maintain CMMs and inspection tools, and inspection stamps are in good condition. • Assist Quality Inspectors with in-process inspection of machined components as necessary • Develop and monitor continuous improvement programs aiming to reduce the number of defects, and improve the overall quality of products • Review engineering changes, product releases, and recommend gages and equipment needed to ensure parts meet tolerances and specifications • Manage interactions with Fralock personnel for quality related issues Required Skills • PC literate (Excel, PowerPoint, Word, e-mail) • Knowledge in blueprint reading basic geometrical tolerances; use of handheld instruments and templates • Good communication and presentation skills both oral and written • Strong initiative, high energy • Technically oriented • Valid Driver License, Auto Insurance & Acceptable Driving Record Preferred Skills 3-5 years CMM programming experience Thorough understanding of GD&T and blue print reading Knowledge in calibration Experience in aerospace, medical or automotive industry Education Requirements High School Diploma Experience Requirements 3 years minimum in a quality/inspection related field Physical Requirements Analyzing Data and Reports Sitting/Walking/Standing Must be able to lift a maximum of 25 lbs. This position must pass post offer drug test, Pre-work Screen, and background check. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of a position. Integrity test and English if applicant does not poses a BA or higher.

Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. With a relentless focus on quality and innovation, Q2 Solutions uses its global experience and scientific expertise to transform science and data into actionable medical insights that help customers improve human health. ?A joint venture of IQVIA (formerly QuintilesIMS) and Quest Diagnostics, Q2 Solutions combines the best of each parent organization?s clinical trials laboratory services capabilities to fulfill its mission of treating each sample as if a life depends on it. Purpose The LIMS Analyst will assist in managing the daily operations of the Laboratory Information Systems (LIS/LIMS).? Collaborates with laboratory end users, IT department, Instrument/LIS vendors, and management as necessary. Responsibilities Monitor system background processes on multiple LIS/LIMS platforms????? Monitor HL7 file transfers and resolve issues as may occur?on multiple LIS/LIMS platforms???? Maintain test code mappings on LIS/LIMS platforms Maintain quality control settings and support LIS/LIMS quality control programs Participate in testing and implementation of LIS/LIMS related application upgrades as may be necessary Manage LIS/LIMS system access requests Manage all aspects of laboratory instrument set-up, maintenance, and troubleshooting Troubleshoot LIS/LIMS Issues Participate and support in management of CAP LIS/LIMS Systems Validation Requirements Submit and manage vendor support requests as may be necessary Required Knowledge, Skills and Abilities Microsoft Word, Excel, PowerPoint, etc. Excellent organizational skills Ability to establish and maintain effective working relationships with co-workers, managers and clients. Knowledge of laboratory equipment, instrumentation and terminology used in the area of responsibility Knowledge of clinical laboratory workflow Background in Information Technology or LIS/LIMS or Laboratory Minimum Required Education and Experience BS degree or equivalent combination of experience and education. Five to eight years? experience in computer system administration, database administration, and software development, clinical, diagnostic or pharmaceutical industry required. Experience with laboratory information systems or laboratory experience is desirable. Excellent verbal and written ability to explain technical concepts. Project management or business analyst skills a plus. Role may require occasional travel IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled IQVIA, Inc. provides reasonable accommodations for applicants with disabilities.? Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA?s Talent Acquisition team at [Click Here to Email Your Resum?] to arrange for such an accommodation. Job ID: R