Manager, Design Salary at Linkedin Corp BETA

Title: Sr. DevOps Engineer Location: Sunnyvale, CA (3 days per week hybrid) Duration: Contract 12+ Months Responsibilities: Infrastructure Management: Design, deploy, and manage scalable, fault-tolerant, and high-performance infrastructure using cloud services (AWS, Azure, or GCP). CI/CD Pipelines: Develop and maintain CI/CD pipelines that enable rapid, reliable, and secure deployments of vehicle software updates. Automation & Documentation: Lead efforts in automating repetitive tasks, improving reliability, and standardizing processes Monitoring and Logging: Implement and manage monitoring, logging, and alerting systems to ensure service health, performance, and availability. Security: Integrate security practices into DevOps processes, ensuring compliance with automotive and software security standards. Performance Optimization: Optimize the performance of infrastructure and applications to meet the rigorous standards of vehicle software. Qualifications: Education: Bachelor’s degree

At Wayve we're committed to creating a diverse, fair and respectful culture that is inclusive of everyone based on their unique skills and perspectives, and regardless of sex, race, religion or belief, ethnic or national origin, disability, age, citizenship, marital, domestic or civil partnership status, sexual orientation, gender identity, veteran status, pregnancy or related condition (including breastfeeding) or any other basis as protected by applicable law. About us Founded in 2017, Wayve is the leading developer of Embodied AI technology. Our advanced AI software and foundation models enable vehicles to perceive, understand, and navigate any complex environment, enhancing the usability and safety of automated driving systems. Our vision is to create autonomy that propels the world forward. Our intelligent, mapless, and hardware-agnostic AI products are designed for automakers, accelerating the transition from assisted to automated driving. At Wayve, big problems ignite us-we embr

🎯 Hiring: Senior Quality Assurance Engineer 📍 Bay Area | Class III Medical Devices | Permanent Position Connect Life Science are partnered with a cutting-edge class III medical device leader developing high risk devices in California. This company is committed to improving patient lives through the development of quality high risk devices. They’re looking for a Senior QA Engineer to drive quality, compliance, and innovation across every stage of product development and manufacturing. 🔍 What You’ll Do: ✔️ Lead and improve QA systems & processes ✔️ Support inspections, audits & compliance efforts ✔️ Drive investigations, CAPAs, NCR and continuous improvement ✔️ Collaborate across Manufacturing, QC, and R&D ✔️ Contribute to Risk Management, design assurance, and validation activities ✔️ Support EU MDR activities ✔️Support eQMS migration ✅ What You Bring: 5+ years in Medical Devices environments Experience with Risk Management, Design Assurance, Test Method Validation, Statistics, CAPA,

🎯 Hiring: Senior Quality Assurance Engineer 📍 Bay Area | Class III Medical Devices | Permanent Position Connect Life Science are partnered with a cutting-edge class III medical device leader developing high risk devices in California. This company is committed to improving patient lives through the development of quality high risk devices. They’re looking for a Senior QA Engineer to drive quality, compliance, and innovation across every stage of product development and manufacturing. 🔍 What You’ll Do: ✔️ Lead and improve QA systems & processes ✔️ Support inspections, audits & compliance efforts ✔️ Drive investigations, CAPAs, NCR and continuous improvement ✔️ Collaborate across Manufacturing, QC, and R&D ✔️ Contribute to Risk Management, design assurance, and validation activities ✔️ Support EU MDR activities ✔️Support eQMS migration ✅ What You Bring: 5+ years in Medical Devices environments Experience with Risk Management, Design Assurance, Test Method Validation, Statistics, CAPA,

Qualifications: BSME, 15+ years of working experience Extensive experience in development of biotech instrumentation with a consumable/disposable component (one-use cartridge...etc.) Strong familiarity of plastic injection molding process, knowledge of tooling design, materials, material properties, DFM Demonstrated experience taking products through R&D and release to manufacturing Experience executing and managing design improvements and changes to units in the field (for sustaining and service) Familiarity with FDA quality requirements (ISO 13485, cGMP, QMS standards, USP class VI (biocompatibility testing)) Proficiency in SolidWorks CAD Responsibilities: Responsible for the design, development, prototyping, and volume manufacturing of complex injection molded assemblies and high-precision mechanical components & assemblies Specifying injection molding tooling with state-of-the-art capabilities: Variotherm, vacuum assist, hot runners, etc Design and development of manufacturing test

Our client is a well-established creative technology company known for building tools that empower visual storytellers. They are in the early stages of building a next-generation cross-platform mobile experience and are seeking a Staff Software Engineer to help lead the development of a new React Native application from the ground up. This is a high-impact role focused on architecting and delivering a performant, reliable mobile platform used by a global creative community. What You'll Do Lead the development of a high-quality React Native mobile app from scratch. Own architectural decisions with a focus on performance, reliability, and scalability. Collaborate closely with product managers, designers, and backend engineers. Implement best practices for testing, CI/CD, and mobile code quality. Mentor other engineers and help shape the engineering culture. Influence the technical roadmap and contribute to long-term platform strategy. What We’re Looking For 10+ years of software engineer

Qualifications: BSME, 15+ years of working experience Extensive experience in development of biotech instrumentation with a consumable/disposable component (one-use cartridge...etc.) Strong familiarity of plastic injection molding process, knowledge of tooling design, materials, material properties, DFM Demonstrated experience taking products through R&D and release to manufacturing Experience executing and managing design improvements and changes to units in the field (for sustaining and service) Familiarity with FDA quality requirements (ISO 13485, cGMP, QMS standards, USP class VI (biocompatibility testing)) Proficiency in SolidWorks CAD Responsibilities: Responsible for the design, development, prototyping, and volume manufacturing of complex injection molded assemblies and high-precision mechanical components & assemblies Specifying injection molding tooling with state-of-the-art capabilities: Variotherm, vacuum assist, hot runners, etc Design and development of manufacturing test

Project Management Advisors, Inc. (PMA) is a national real estate advisory firm providing consulting services as the owner's representative, including development management, project management, program management and investor representation. Recognized among the commercial real estate industry's top professional services firms, including being named to Engineering News-Record top CM firms for the past four years in a row, we partner with our clients as their unbiased advocate to provide leadership and strategic guidance for increasingly sophisticated real estate needs and challenges, minimizing risk while maximizing outcomes. CREATE YOUR FUTURE WITH PMA Curious to stimulate your career growth through meaningful mentorship and thoughtful training? Are you interested in collaboration, working as an integral part of a team to deliver complex real estate projects across the country? Are you diligent, enthusiastic, and eager to work with clients having an impact? Project Management Advisor