Quality Assurance Engineer Salary at 340Basics BETA

Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care. SUMMARY DESCRIPTION The Quality Assurance Engineer II will provide Quality compliance support on all aspects of the Plainsboro, NJ CMC Quality System. The Quality Assurance Engineer II will monitor, prioritize and track the timely closure of NCs and CAPAs for the Plainsboro Plant facility, participate in problem solving teams, and participate from a Quality Engineering & Quality Systems and Plant perspective on the launching of new or improved products/processes. He or She will act as a Quality Reviewer for NCs and CAPAs, in addition to being responsible for the quality efforts in other areas of the NC/CAPA syst

Overview: FUJIFILM Irvine Scientific, Inc. is a worldwide leader in the innovation and manufacture of cell culture media, reagents, and medical devices for researchers and clinicians. The company provides unrivaled service and quality to scientists working in biopharmaceuticals, cell therapy, regenerative medicine, assisted reproductive technology and cytogenetics, and industrial cell culture for the large-scale production of biotherapeutics and vaccines. Fujifilm Irvine Scientific adheres to ISO and FDA regulations and operates dual cGMP manufacturing facilities in California, USA, and Tokyo, Japan. The companys consultative philosophy and expertise in cell culture and compliance provide customers with unique capabilities and support. For over 50 years, Fujifilm Irvine Scientific has remained uniquely flexible and focused on media while becoming a strategic global leader in media products and services. FUJIFILM Irvine Scientific, Inc. is a subsidiary of FUJIFILM Holdings America Corpo

Design test processes, frameworks, and workflows that ensure consistent quality delivery. Lead QA engineers and automation specialists. Develop and execute QA strategies and test plans. Define test objectives, scope, and resource allocation based on project requirements. Identify and mitigate risks related to quality and testing. Oversee manual and automated testing processes, ensuring testing is done efficiently and effectively. Ensure automation coverage and develop a strategy for automated test scripts and frameworks. Review and optimize the existing test automation suite for better performance and maintenance. Manage testing efforts for different types of testing (functional, integration, regression, performance) Collaborate with developers, product managers, and business analysts to ensure requirements are clear and quality standards are defined early in the development lifecycle. Participate in design reviews and sprint planning sessions to define testable user stories and accept

Cadent ignites seamless connections between brands, publishers & consumers. Our predictive AI orchestrates outcomes on any platform customers are on, across any media they consume & at any stage of the journey. To learn more, please visit thenewcadent.com Right now we are looking for a highly motivated and experienced Senior Director of Data Science within the Data Services Organization who will be responsible for shaping our data science strategy, managing a team of data scientists, delivering ML products and collaborating with cross-functional teams to translate data into actionable business strategies. The Sr. Director will apply scientific methods to identify business optimization strategies and develop, evaluate, and demonstrate prototypes and production grade builds. Data Scientists collaborate directly with the Business, Product, Data Engineering, DevOps and QA team members to productize AI/ML research to drive business growth. This is a critical role that needs knowledge of mat

**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

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

About the Role: Grade Level (for internal use): 09 The Team: Our team emphasis on shared goals, trust and open communication, which foster a cohesive and productive environment. Our team dynamics value elements like accountability, creating a culture that promotes innovation, motivation and resilience in the face of challenges. Responsibilities and Impact: S&P Global is seeking to hire QA Engineers for open positions at their New Jersey office. The new Scrum Master will be working on SAFE AGILE teams and would be participating in Requirement refinement and would be developing and executing Test plan to ensure Product quality. Strong Analytical skills and experience with automation testing tools are essential. Join us to help deliver on exceptional products that meet the highest standards of quality and performance. Compensation/Benefits Information: (This section is only applicable to US candidates) S&P Global states that the anticipated base salary range for this position is $90,000 t

Hybrid: 2-3 days onsite in New Jersey Summary: The QA Engineer I is responsible for testing and ensuring software quality at various stages of development. They will design and execute test plans, develop and maintain automation scripts, identify and document defects, work with cross-functional teams to maintain software quality, and provide feedback to developers on ways to improve the software. The QA Engineer I is also responsible for staying informed about new testing tools and methodologies, as well as industry trends. They may perform manual and automated testing, as well as API, performance, and database testing. Essential Job Duties and Responsibilities: Execute detailed test plans and test cases, focusing on both manual and automated testing. Participate in API testing using tools like Postman to ensure API reliability and performance. Manage and execute test cases using Zephyr, integrating testing tools with JIRA for efficient defect tracking. ssist in the development and mai