Audit Salary at Itrenew Inc BETA

At **APTIM** , we come to work each day knowing that we are making an impact on the world. Our work spans from safeguarding and maintaining critical infrastructure to helping communities recover from natural disasters, from empowering our armed forces and first responders to reducing carbon and energy use, and from making cities more resilient against the threats of climate change to restoring contaminated ecological systems. **Job Overview:** APTIM has openings for a Environmental Technician to work in a team to perform solid waste composition assessments of client waste containers ranging in size from 3 cubic yards to 40 cubic yards. These assessments are typically 1-2 days in duration with typical team sizes ranging from 2 to 5 depending on the size of the assessment. Work activities will include sorting through solid waste using hand tools to segregate waste items by type for the purpose of assessing various types of waste including plastics, paper, cardboard, glass, food waste and

Overview: Frank, Rimerman + Co. LLP is seeking driven, passionate, and collaborative individuals to join our expanding Corporate Audit practice. This position can be based from our San Jose or San Diego office with the expectation to be in-person three days per week on average. The group start date will be early September 2025. Our Corporate Audit group focuses on emerging to late-stage startups pursuing ambitious growth and exit strategies. Our environment enables you to interact directly with these influential clients and see what is up and coming in Silicon Valley. Working with these industry disrupters and serial entrepreneurs, we support our clients beyond delivering an audit by also providing operational insight as they face market challenges. As an Audit Associate you will develop the technical, professional, leadership and interpersonal skills that will help you establish a successful and long-lasting career! Responsibilities: Attending client meetings and engagement planning m

Job Title: Senior Supplier Quality Engineer Department: Quality Assurance Engineering Job Overview: The Senior Supplier Quality Engineer (SQE) specializing in Printed Circuit Board (PCB) fabrication will play a pivotal role in ensuring the quality of supplied PCBs, driving supplier quality improvement, and supporting supplier development activities. This position involves working closely with cross-functional teams, including Engineering, Supply Chain, and Suppliers, to uphold quality standards and drive continuous improvement. Reports to Sr. Manager, QE and QA Located in Newark, CA Primary Job Responsibilities: 1. Supplier Quality Management: Evaluate and qualify new PCB suppliers and other material suppliers, including audits and performance assessments. Develop and implement supplier quality plans in alignment with organizational goals. Establish key performance indicators (KPIs) for suppliers and monitor adherence to quality standards. 2. Supplier Quality Control Review and approve

Job Description: Shift Hours: 6-4:30 PM PST+ OT as needed. Responsible for the final quality audit before shipment of systems, upgrades, and miscellaneous ship kits. Collaborate closely with Manufacturing, Manufacturing Engineering, Master Scheduling, Production Control, Material handlers, Dock personnel and Packing contractors to ensure audits and quality inspections are completed so that products ship on time. Demonstrate proficiency with SAP SW as well as the MS Office suite. Clear communication and strong collaborative skills Persevere against challenging and time constrained issues. Inventing creative solutions to problems to ensure the job gets done on time. Provide constructive process improvement recommendations. Redline procedures as appropriate. Assist in the training and development of new hires. Support other product lines in plant clearance activities when necessary. Responsibilities: Auditing material against BOMs. Evaluating the quality of packaging. Visual spot check of

Join our select group of Deloitte Discovery interns, and you'll get an inside look at what it's really like to work for a professional services organization. The Discovery Internship is open to all eligible students. Because of our desire to have a diverse slate of candidates, students who identify as Black or African-American, Hispanic or Latinx, American Indian or Alaska Native, Native Hawaiian or Other Pacific Islander, or two or more races are encouraged to apply. Recruiting for this role ends on May 1, 2025. Work you'll do Throughout the course of the seven-week internship, interns are assigned to one or more client projects where they will receive mentorship and support to help their success on the engagement. Beyond exposure to "real life" projects, the internship also delivers a variety of national and local learning and networking events. In addition, throughout the internship there are ongoing learning events such a lunch and learns, industry/service line spotlights, and regu

About the job Gxp Auditor GxP Auditor is an integral member of the Quality and Compliance team. The GxP Auditor is responsible for planning and conducting scheduled quality audits on behalf of RxCloud. This position will also act as a Subject Matter Expert (SME) for GxP auditing and quality projects. It will be responsible for supporting the ongoing development and management of the Quality Management Auditing system. This position is responsible for independently managing quality/GxP auditing deliverables scheduled. Responsibilities Include •Function as a Quality/GxP auditor of both external CDMOs and clinical sites, and internal laboratory operations. •Develop and implement the global audit strategy, aligning with organizational goals and regulatory requirements. •Perform audits across various departments and functional areas. •Conduct risk assessments to identify potential areas of concern and develop appropriate audit plans and procedures. •Review and assess the effectiveness of in

Description This position supports the Clinical Quality Assurance function by providing GCP compliance oversight and support to Arcus Clinical Development therapeutic areas. The key activity of the role is providing expertise and guidance regarding applicable regulatory, Good Clinical Practice, and Arcus Standard Operating Procedure requirements for the conduct of clinical studies. Primary responsibilities will include working with study management teams to facilitate internal and external adherence to Quality and Regulatory Compliance by ensuring conformance to domestic and international quality regulations and GCP guidelines. This role may also participate in investigator site audits, internal functional/process audits, and clinical vendors (GCP, GCLP, GPvP) as assigned. As a GCP compliance expert, the Associate Director (AD) Clinical Quality Assurance (Study Compliance) will utilize a risk-based and phase-appropriate strategy to prioritize GCP QA support for clinical functions, iden

A World-Changing Company Palantir builds the world's leading software for data-driven decisions and operations. By bringing the right data to the people who need it, our platforms empower our partners to develop lifesaving drugs, forecast supply chain disruptions, locate missing children, and more. The Role As a Financial Audit Manager, you'll report to the Head of Financial Audits and partner together to build and mature our SOX and Financial Compliance Internal Audit program. You'll be responsible for managing activities relating to financial compliance with applicable laws and regulations, particularly requirements as defined by Sarbanes-Oxley (SOX) and Generally Accepted Accounting Principles (GAAP). This role involves extensive collaboration with teams across Palantir, including Finance, IT and Legal. In partnership with the Systems and Technology Audit team, you'll work on maturing the SOX compliance program and execute against it in a high-growth environment. You will be respons