QA Engineer Salary at Health Union Llc BETA

Job Description: QA Engineer About the ChargeItSpot Team ChargeItSpot is a leader in mobile device solutions. For over a decade, our intelligent locker systems have tackled real-world challenges. We started off by helping people with free and secure charging for their dying phones. Today, our intelligent, locker-based kiosk solutions are thoughtfully designed to streamline the management of enterprise-owned mobile device fleets. At ChargeItSpot, we surround ourselves with independent thinkers who are detail-oriented, and customer obsessed. Our clients have routinely called us “the most talented team they’ve ever worked with.” We value determination, resourcefulness, imagination, and follow-through. We want people who are ready to get things done. Our focus is fierce, but it’s not all hard work. We take time to get to know each other through a daily game of Jeopardy, meals together, and nights out for karaoke. We operate a hybrid work model, with most team members working in the office

Automation Engineer Philadelphia, PA 12 month rolling contract Job Overview: This role involves specifying, procuring, and installing new equipment in an aseptic manufacturing facility. The engineer will also be responsible for reviewing designs for new equipment and modifying existing systems. Key responsibilities include managing equipment and facility projects from initiation to completion, determining change control requirements, ensuring pre-approval compliance, and supporting validation protocol execution. Strong written and verbal communication skills are essential, along with excellent project management abilities, including proficiency in MS Project. Experience in PLC and HMI programming is required. Compliance with cGMP and EU regulations must be maintained. Responsibilities: Lead and oversee site projects by leveraging experience, research, design concepts, sketches, layouts, and vendor collaboration. Develop specifications, consult with management and site personnel, and en

**General Description:** This role provides a good opportunity for setting a new analytical lab and engaging analytical test method transfer for late phase clinical phase/commercial products as a senior analytical scientist in BeiGene Manufacturing Science and Technology team (MST) located in Hopewell NJ. The senior scientist will manage equipment IOQ, then design, execute, and document comparability test for analytical method. Also, the test for small scale samples from MST upstream and downstream parts by transferred analytical method. The position requires experience in quality control team or analytical team in process development or similar team in biological pharmaceutical or life science company. The candidate must have experience working with cross-functional stakeholders and demonstrated ability to thrive in a fast-paced, matrixed environment. **Essential Functions of the job:** + Planning, implementing, and reporting technical transfer for physiochemistry and biochemistry met

Job Summary As a software engineer with a testing focus on the customer facing- digital solutions team you will collaborate with a skilled group of engineers dedicated to enhancing the core customer experience. This team focuses on improving the Android and iOS mobile applications, as well as the MyAccount web application, ensuring a seamless and intuitive user experience across all platforms. They collaborate with on-team QA Engineers and developers to develop an automation strategy that can facilitate shortened test cycles and add value through quality coverage. Additionally, they drive forward testability solutions and lead automation strategies across CCI. Responsibilities Acts as the technical expert providing direction on problems of systems integration testing and compatibility. Collaborate across teams to drive forward automated strategies and innovate upon our approach to quality. Develop automated checks within the domain framework for API as well as UI. Deliver automation st

About the job Technical Lead (Healthcare IT Solutions) Roles & Responsibilities: Lead an agile team of developers, QAs and cloud architects designing clinical data solutions Prior experience in building solutions for Epic EMR clinical data access and integrations Leverage expertise in patient health data from HL7, FHIR and other clinical interoperability platforms Foster a culture focused on delivering high quality and complex clinical analytics solutions Hands-on technical leadership in solution architecture, design and delivery leveraging Angular and NodeJS Grow team capabilities aligned to the latest clinical data compliance, privacy and web technology skills Understands the projects under their purview and can identify resource risk, skillset risk, and work with delivery leadership on hiring plans. Ability to understand technical architectures and ensure quality excellence based on the guidelines provided by CTO office Required Skills and Qualifications: 10-15 years of technology l

Job Title: IT Quality Assurance Manager Schedule: Monday-Friday 8:00am - 5:00pm Location: Willingboro, New Jersey (required full time on site) Radwell International is seeking a highly skilled and motivated IT Quality Assurance (QA) Manager to lead our QA team in ensuring the quality, reliability, and performance of our IT systems, software, and applications. The IT QA Manager will oversee all aspects of quality assurance, focusing on manual testing, test planning, strategy, and team leadership. This role requires strong technical expertise, excellent leadership skills, and a deep understanding of QA methodologies to support the successful delivery of high-quality IT solutions. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following: Develop and implement comprehensive QA strategies for software, systems, and applications across the organization. Collaborate with stakeholders (developers, product managers, business analysts) to define test requirements, test plans, and acceptance c

The Document Control Specialist II maintains control of all quality documentation. This position works independently, with minimal supervision, in accomplishing daily tasks and advising others. This position works closely with all departments to maintain a compliant program. This position is responsible for organizing, maintaining, and updating all controlled documents. All functions of the document center must be in compliance with quality system GMP, 21 CFR 820 (FDA), ISO 13485 and other quality standards. This position actively and independently leads projects with minimal support within established deadlines and expectations. The Document Control Specialist II: Processes, releases, and Controls Engineering Change Orders. Responsible for creating part numbers and Bill of Materials (BOMs) in the ERP system. Processes, maintains, and monitors deviations Processes, releases, and Controls all Quality documents (e.g. Standard Operating Procedures (SOPs), Risk Management Documents, Techni

QA Engineer - Malvern, PA RAJANT CORPORATION, the 20+-year leader in industrial wireless patented Kinetic Mesh® networking solutions, providing full mobility and autonomous products, is seeking a QA Engineer to evaluate our firmware and software through rigorous testing processes. This includes performing regression testing, assessing new features and bug fixes, triaging software bugs, and developing automated test scripts. The role also involves continuous improvement of our internal development and testing processes. Key Responsibilities: Develop & Execute Test Plans: Design, develop, & implement comprehensive test plans & test cases to ensure product quality & compliance with specifications. Automate Testing Processes: Create and maintain automated test scripts using Bash and Python to streamline testing procedures and improve efficiency. Bug Identification and Triage: Identify, document, and prioritize software defects; collaborate with the development team to facilitate timely res