Analyst Intern Salary at Linkedin Corp BETA

Who We Are Buro Happold is a global leader in sustainable and resilient building design. We work at the cutting edge of engineering, where your creativity and expertise are crucial to developing groundbreaking solutions. Our portfolio includes innovative works across the US and around the world, from the Hard Rock Hotel at Metropolitan Park to the NEOM Line. We offer unparalleled opportunities for personal professional growth and the chance to contribute to a more equitable world. As a Senior Engineer or Associate Vertical Transportation Consultant you will have the opportunity to apply your technical knowledge across a portfolio of ground-breaking projects in the US and globally. Strong communication skills and teamwork are essential to life at Buro Happold and in turn, we can offer you unrivalled career, project, and development opportunities. Responsibilities: As a Vertical Transportation Consultant and key member of our North American Specialist Team, you'll lead the design and dev

Job Description Job Description Work Location: Sunnyvale, California Salary Range: $80,000 - $140,000 Job Type: Full-Time Onsite Our Company: Founded in 2010, iHealth Labs is dedicated to empowering people to live healthier lives. The company is a leading provider of cloud-connected medical devices, personal health care devices, and home-based tests and is at the forefront of the digital health revolution. In November 2021, iHealth's COVID-19 Antigen Rapid Test received Emergency Use Authorization from the U.S. Food and Drug Administration for over-the-counter sales. Since then, iHealth has become a key supplier of at-home COVID tests to the federal government, state governments, nonprofits, and individual consumers. iHealth Labs is a leader in digital health solutions, with a mission to revolutionize the healthcare industry by making quality health management accessible and affordable for all. Job Responsibilities: In this role, you will be part of the regulatory team responsible for

Position: Quality Management Specialist Location: Hybrid in San Jose, California Duration: 2 year contact + ongoing Hourly: Up to $65 - 75/hr Openings: 1 Interview Process: 1 round interview process Required Skills & Experience Bachelors Degree in Business Management, Industrial Engineering, or Quality Management 3-5 years' experience supporting project management, technical support, business process improvement, or a Quality Management System in the semiconductor industry or equivalent 3-5 years of experience using quality concept tools and techniques: Pareto, Cause & Effect Diagrams, control charts, Six Sigma, Lean, Benchmarking, Root Cause Analysis) Internal Auditor or Lean auditor for TL9000 or ISO9001 Management Systems within the Semiconductor or electronics industry Data manipulation and analysis using: Excel & PowerBI Nice to Have Skills & Experience Sigma Certification Job Description Insight Global is seeking a Quality Management Specialist to work onsite for one of the large

Job Summary Reporting into the Director of Procurement for Mass Storage Commodities, the Procurement Analyst intern will: Partner with the SSD Procurement Manager and lead a key project impacting the bottom line Lead the SSD cost forecasting project. The project involves building a tool to predict SSD pricing by aligning relevant inputs and by leveraging advanced statistics/AI/ML tools. The goal for the tool is to provide a relatively accurate NetApp point-of-view of the SSD market and pricing Develop an understanding of our Procurement, Supply Chain and Systems and Tools processes and identify targets for improvement in transactional and operations efficiencies Support the SSD Procurement manager with coordinating supplier meeting/negotiations and ad hoc analysis around spend/cost projections Job Requirements Must haves: strong analytical skills, great communicator, eagerness to collaborate cross-functionally, looking for a fast-paced environment Nice to haves: degree in engineering/s

At Bloom Energy, our vision for a world powered by clean, reliable, and affordable energy is more than just a dream-we're making it reality. For over two decades, we've been at the forefront of the global energy transition, pioneering solutions that empower critical industries to thrive in a rapidly digitizing, energy-intensive world. From revolutionizing power for AI-driven data centers to ensuring resilience for hospitals, electric grids, manufacturing facilities, and utilities, our solid oxide fuel cell (SOFC) and solid oxide electrolyzer (SOEC) technologies are redefining what's possible by delivering energy abundance for all. With more than 30,000 fuel cell modules deployed worldwide, we are the trusted partner for Fortune 100 companies and innovators alike. Our cutting-edge solutions enable unparalleled "time-to-power" capabilities, reliability, and sustainability, ensuring our customers remain ahead in a world where soaring energy demand and intensifying energy scarcity are rapi

Associate Director of Process Development and Documentation | Clinical Quality Assurance (CQA) Professional Summary: A highly experienced Clinical Quality Assurance professional with over 10 years of expertise in developing and maintaining clinical research SOPs, process development, and compliance for clinical-stage pharmaceutical companies. Proven leader with strong technical writing skills, capable of working cross-functionally to ensure adherence to industry standards and regulatory requirements. Experienced in managing audits, inspections, and continuous improvement of the Quality Management System (CQMS). Key Skills & Expertise: Process Development & Documentation: Expertise in developing and maintaining GCP, GLP, and GVP processes and SOPs. Adept at mapping and documenting clinical processes for clinical trials. SOP Writing & Compliance: Strong experience in developing and reviewing SOPs, ensuring compliance with regulatory guidelines, and maintaining review timelines. Inspectio

The Associate Director of SOP and Process Development in Clinical Quality Assurance (CQA) is a key member of the CQA team and will lead day-to-day clinical quality operations and compliance activities related to the development and documentation of processes that support successful execution of clinical studies. Responsibilities: Lead process development and documentation activities in collaboration with Clinical Development functional teams to support clinical study success Manage and/or lead cross-functional teams to develop SOPs aligned with GCP, GVP, and GLP requirements Partner with functional teams to guide process development, SOP writing, and ensure timely SOP reviews and updates Serve as a subject matter expert for SOPs and provide process compliance guidance to clinical study teams Participate in the review and approval of clinical study documents and SOPs/Guidance Documents as needed Develop and manage SOP timelines to ensure adherence to review cycles and regulatory-driven

At Juniper, we believe the network is the single greatest vehicle for knowledge, understanding, and human advancement the world has ever known. To achieve real outcomes, we know that experience is the most important requirement for networking teams and the people they serve. Delivering an experience-first, AI-Native Network pivots on the creativity and commitment of our people. It requires a consistent and committed practice, something we call the Juniper Way. Forensic Analyst Intern Are you interested in forensic science and looking to gain valuable skills and hands-on experience in a forensic lab? Join our team as an intern and contribute to essential evidence management and digital forensics tasks! We at Juniper Networks are seeking continuing students who are interested in a forensic analyst Summer 2025 Internships. We're looking for people who are excited about forensic science and eager to gain practical experience in a forensic lab setting. As an intern, you will have the opport