Quality Auditor Salary at Clarus Rcm Inc BETA

Education/Special Training Required * Bachelor of Science, Engineering or related subject with 2 or more years of experience in a quality or engineering discipline in a manufacturing environment, or * Master of Science, Engineering or related subject with 0 or more years of experience in a quality discipline Qualifications/Work Experience Required Who We Want A Quality Engineer with the ability to drive quality and deliver results. Someone who is an advocate for quality and lean methodologies; a self-directed professional who can identify issues and communicate effectively to all levels within the organization; a medical device industry professional who is passionate about providing superior quality products to patients and customers. * Previous experience in a regulated environment desirable (e.g. Medical Device, Aviation, Aerospace, Automative, Defense). * CQE or equivalent course work / experience desirable * Proficient in understanding of Med Device manufacturing processes desirabl

**Job Description Summary** The Manager, Quality Assurance reports directly to the Associate Director, Plant QA and is responsible for managing the quality activities and personnel for multiple departments in the plant. The manager will coordinate efforts for corrective and preventive action, non-conforming material investigations, and internal and external audits. They will assure manufacturing and support areas are compliant to regulations, standards, and internal procedures. The manager will support continuous improvement activities for the manufacturing and quality systems. They will provide regular updates to management of trends from these areas and oversee training and development activities for quality personnel in area. **Job Description** We are **the makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and its no small feat. It takes the imagination and passion of all of usfrom design an

**Description** **You Lead the Way. Weve Got Your Back.** With the right backing, people and businesses have the power to progress in incredible ways. When you join Team Amex, you become part of a global and diverse community of colleagues with an unwavering commitment to back our customers, communities and each other. Here, youll learn and grow as we help you create a career journey thats unique and meaningful to you with benefits, programs, and flexibility that support you personally and professionally. At American Express, youll be recognized for your contributions, leadership, and impactevery colleague has the opportunity to share in the companys success. Together, well win as a team, striving to uphold our company values and powerful backing promise to provide the worlds best customer experience every day. And well do it with the utmost integrity, and in an environment where everyone is seen, heard and feels like they belong. **About the Internal Audit Group at American Express**

About the job QA/QC Technician Conduct thorough inspections and audits of all solar projects during various stages of construction and operation. Prepare and send material requests to PM (or directly to Procurement as agreed with PM). Oversee EPC Contractors QA/QC process specific to piles, racking systems, modules, harness/collection systems, inverters, AC/DC wiring systems, substation, transmission line, fencing, SWPPP and perform daily inspections. Perform quality control checks on materials, components, and equipment used in solar installations to ensure compliance with project requirements and industry standards. Electronically log, organize, and track all issues/deficiencies found during inspections. Collaborate with project managers, engineers, and contractors to address and mitigating any quality related issues, nonconformities, and corrective actions in a timely manner. Manage the punch list and inspection process for efficient project closeout. Stay informed about industry tr

Company Description RRD is a leading global provider of marketing, packaging, print, and supply chain solutions that elevate engagement across the complete customer journey. The company offers the industry's most trusted portfolio of creative execution and world-wide business process consulting, with services designed to lower environmental impact. With 22,000 clients, including 93% of the Fortune 100, and 32,000 employees across 28 countries, RRD brings the expertise, execution, and scale designed to transform customer touchpoints into meaningful moments of impact. Job Description JOB SUMMARY Responsible for machine operation and crew in a light industrial setting. Must manage machine team to ensure proper and safe operation of assigned equipment. Responsible for quality, output, and meeting production goals. Additionally, fulfills the job duties of a Production Technician 1 and 2 as required. 2nd Shift Start Time: 7:15PM - 5:45AM KEY DUTIES/RESPONSIBILITIES Production: Monitors perfo

Description Schedule :Monday - Friday (40 hrs/wk)8:00 AM - 5:00 PM Department: Quality Systems & Support - 252 Primary Purpose : The Quality and Regulatory Affairs Specialist I monitors and coordinates organization-wide compliance to current requirements of all quality related regulatory, certifying, licensing, and accrediting agencies. The Quality and Regulatory Affairs Specialist I assists with the coordination and maintenance of the regulatory submissions for new certificates, licenses, and updates to laboratory director roles with accrediting agencies. They may operate as a primary point of contact with regulatory agencies including but not limited to: CAP, CLIA, CMS, FDA, NY, ISO, DNV, and California. The Quality and Regulatory Affairs Specialist I frequently supports regulatory activities and supports ARUPs quality management System (QMS). This may include maintaining accuracy of the laboratory activity menu, coordinating or oversight of proficiency testing functions, coordinatin

Location: ONSITE – West Valley City, Utah (84119) Duration: 12 months - Estimated to end 4/2026 (Contract extension and/or internal hire possibilities) Type: W2 contract (Third-party or C2C "Corp-to-Corp" arrangements WILL NOT be considered for this role) Pay: Negotiable depending on direct-related experience Work Authorization: Must be currently in the United States with active employment authorization documents. Visa sponsorship is not available, now or in the near future, for this position. Job Summary: Seeking an experienced Quality Engineer with the ability to drive quality and deliver results. Someone who is an advocate for quality and lean methodologies; a self-directed professional who can identify issues and communicate effectively to all levels within the organization; a medical device industry professional who is passionate about providing superior quality products to patients and customers. Duties include: Work closely with operations and the business functions to ensure qu

Boccard Life Sciences, industrial integrator located in 35 countries, designs, manufactures, assembles, and installs process solutions for its customers worldwide in the Food & Ingredients, Pharmaceutical, Cosmetics, and Brewing Industries. Safety & Quality Manager The Quality and Safety Manager plays a pivotal role in overseeing and enhancing environmental health and safety initiatives within the organization. They are tasked with coordinating and executing programs to ensure compliance with regulatory guidelines and company policies, particularly focusing on the Boccard Management System (BMS) and the Boccard Project Management System (BPMS). Reporting directly to the Chief Operating Officer, the Quality and Safety Manager is responsible for monitoring and addressing non-quality costs across the entire Business Unit (BU), with a primary objective of fostering continuous improvement. The overarching objective of the Quality and Safety Manager is to facilitate continuous improvement wi