Quality Technician Salary at Delkin Devices Inc BETA

SCOPE: This opportunity will support efforts to ensure customer requirements are met and improve quality of products and processes throughout the organization by performing inspections. Identifying areas for improvement and implementing effective, permanent and systemic solutions in support of the business. RESPONSIBILITIES: Develops, maintains, and generates CMM programs used to inspect and verify production Perform product inspections in accordance to drawings, routings and customer requirements. Measures, tests, and monitors product and process quality. Assists in Developing, maintaining IM Keyence programs Create Certificates of Conformance / Cert Packages Safeguards our customers from receiving poor quality product. Other duties and responsibilities may be added, deleted or changed at any time at the discretion of management, formally or informally, either verbally or in writing. PHYSICAL REQUIREMENTS: Requirements include the lifting / moving up to and including 50 lbs. Standing,

Quality Assurance Specialist The Opportunity: As the quality assurance expert, you'll work with engineering, operations, support services, cybersecurity, and program management team members that evaluate developed systems for the organization. You'll review, develop, and implement documentation based on requirements of processes, products, and deliverables. Using analysis of established program documentation, you'll generate problem resolutions and track quality assurance standards to observe how the organizational processes and products are measured, then document the results and communicate defects to the functional teams so they can start improving any non-compliant issues. You'll expand upon your experience in various types of process improvement, to include sharing best practices, metrics analysis, and lessons learned. This is an opportunity to broaden your skills in documenting and solving system and process deficiencies. Work with us to develop systems solutions that secure our

Responsibilities: This is for potential upcoming opportunities. We will review your resume and reach out when an opportunity is available. Electronic Engineering/Quality Assurance Noblis MSD is seeking candidates for Electronic Engineering/Quality Assurance to support the Naval Information Warfare Center, Network Integration Engineering Facility (NIEF). The Associates will be responsible for the inspections and reviews of the various networks, programs, and communication systems for the NIEF. This includes but not limited to: the quality assurance and the quality control of all incoming, in process, and final delivery systems, to provide the highest level of quality products to our customers. The Associates will also develop and review reports and statuses for all quality related encounters. This is a full time / on-site position in San Diego, CA. Responsibilities: Responsible for the coordination and the completion of tasks assigned, and duties specific to the NIEF QA team. Read and u

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. Summary The Production Quality Specialist 3 ensures the quality and compliance of manufacturing operations and products. This requires resolving nonconformities and implementing effective CAPAs. Additionally, the Production Quality Specialist is responsible for upholding and improving quality standards, procedures, and systems. Responsibilities Ownership, management, and processing of nonconformances, Out-of-Tolerance Reports, and CAPA records. Identifies and drives appropriate corrective and preventive actions to prevent recu

EOE Statement We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law. Description GENERAL SUMMARY: Understand and enforce the Quality Assurance (QA) program to ensure company production efforts are compliant with customer directives, requirements, specifications and the Quality Management System. Ensure the requirements set forth in the company processes and QA Manual are adhered to and enforced. Ensure support processes comply with the Quality Management System. Other duties include working in a Tiger Team work environment. Travel and overtime may be required. Strong analytical skills required. LOCATION: San Diego, CA. REQUIREMENTS: Must be a U.S. Citizen Experience reviewing QA Workbooks or similar High level of familiarity with NAVSEA STD Items, MIL-SPECS, and TECH PUBS app

Overview: Exagen is a patient-focused and discovery-driven life sciences company dedicated to transforming the care continuum for patients suffering from debilitating and chronic autoimmune diseases. Our goal is to enable rheumatologists to improve care for patients through the differential diagnosis, prognosis, and monitoring of complex autoimmune and autoimmune-related diseases, including lupus and rheumatoid arthritis. By leveraging our proprietary Cell-Bound Complement Activation Products, or CB-CAPs, technology, we help get to the real cause of a patients symptoms and guide their journey to improved health. Under the supervision of the Quality Systems Manager, the Quality Specialist will support company-wide initiatives to maintain the highest standards of quality care and ensure adherence to regulatory requirements. Responsibilities: Note: Other duties may be assigned. Respond to Document Control related activities throughout the site. Manage training documentation and track empl

Quality Assurance Specialist, Clinical Supplies Position Summary: Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. Catalent Pharma Solutions in San Diego is a premier pharmaceutical chemistry development and manufacturing organization supporting the pharmaceutical and biotechnology industries. We focus on bringing client drug compounds from discovery to the clinic with services that include analytical development, pre-formulation testing, formulation development, GMP (Good Manufacturing Practices) manufacturing and stability storage and testing as well as Clinical Supply Services. At Catalent San Diego, we recruit and develop exceptional individuals with a passion for science and determination to excel. We offer a technically challenging and stimul

Job Title: Senior Level Quality Assurance Specialist Job Description Thomson is looking for a Lead Specialist in Quality Assurance to join our dynamic and growing team. This role is crucial for maintaining our high standards of quality and ensuring compliance with ISO certifications. The ideal candidate will be a seasoned professional with a strong background in quality assurance, documentation control, ISO/GMP certifications, and audits. Hard Skills + High-level experience in Quality Assurance + Expertise in documentation control + Proven experience with ISO and GMP certifications + Experience with internal and external audits Soft Skills + Bilingual Spanish speaking (Nice-to-Have) Job Type This is a contract position with a duration of 6 Month(s). Work Site This is a fully on-site position in Oceanside, California. Work Environment Location: Carlsbad, CA (with a small chance of Oceanside, CA) Schedule: Monday to Friday, 8 AM - 5 PM (On-site only) About Actalent Actalent is a global l