Quality Assurance Engineer Salary at Health Union Llc BETA

Quality Assurance Supervisor A growing ophthalmic medical device company is seeking a quality assurance leader to join their organization in a crucial position. This role is vital for ensuring the highest standards of quality and regulatory compliance within the company. Role and Responsibilities Oversee the company's quality system to ensure compliance with FDA, ISO, CE, and Health Canada certification regulations, including maintaining registrations with these entities. Act as the Management Representative, keeping management updated on new regulations and the company's compliance status. Serve as the person responsible for regulatory compliance (PRRC), ensuring devices meet conformity standards, proper identification (UDI) before release, and managing post-market obligations. Handle customer complaints, including Medical Device Reporting and fulfilling Vigilance requirements. Manage activities and documentation related to Corrective/Preventive Actions. Oversee the Document Control S

Location: 1 day per MONTH onsite in Philadelphia - remote the rest of the time Day-to-Day: One of our largest clients is looking for a Senior Delivery Manager to join their dynamic team. As a Delivery Manager/Scrum Master, you will oversee multiple squads, ensuring smooth execution within the Agile Scrum framework. You’ll manage dependencies across global teams, escalate blockers, and provide actionable insights through Jira and other reporting tools. This role supports a platform that helps students find study materials, take notes, create flashcards, and complete assessments, with instructors using it for testing. You’ll collaborate across time zones with a Product Manager in France, engineers in Ukraine, and a Lead in the U.S. The team includes 6–8 engineers (growing to 12), 2 QA engineers, a Dev Lead, and Delivery Managers in each dependency team. Strong coordination and communication are key to success. While this role is remote, EST working hours are required. Compensation: $110,

Description Quality Assurance Associate I, PHL Main Duties and Responsibilities 1. Implement, communicate and maintain company's quality systems at the facility, in compliance with Marken's Global Quality Management System (QMS) requirements. 2. Interact with clients on Quality Assurance (QA)/ GxP related matters under management supervision. 3. Effectively interact with Marken Departments and stakeholders to maintain that all QA tasks are appropriately supported by QA. 4. Support on internal audits including report preparation and assessment and tracking of associated corrective and preventive actions (CAPA). 5. Support audits of external service providers as part of the vendor selection process. Follow up and tracking all commitments for actions or changes made by Marken from previous audits, including report preparation. 6. Support client audits and regulatory inspections, including the preparation of appropriate materials required within those audits when applicable. 7. Collate iss

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 Description Job Description Key Responsibilities Mechanical Assembly Assemble mechanical components, subassemblies, and complete systems based on detailed blueprints, technical drawings, and assembly instructions. Use hand tools, power tools, and precision instruments to fit, align, and secure components. Wiring and Electrical Assembly Install and connect wiring harnesses, sensors, and electrical components. Test electrical connections to ensure functionality and troubleshoot basic electrical issues as needed. Hydraulics Assemble and connect hydraulic systems, including hoses, pumps, valves, and fittings. Test hydraulic components for proper operation, identifying and resolving any leaks or performance issues. Quality Control Inspect parts and assemblies during and after production to ensure compliance with quality standards. Identify and report defects or discrepancies to the Manufacturing Director. Documentation and Reporting Maintain accurate records of assembly processes, inclu

Req ID:468345 At Alstom, we understand transport networks and what moves people. From high-speed trains, metros, monorails, and trams, to turnkey systems, services, infrastructure, signalling and digital mobility, we offer our diverse customers the broadest portfolio in the industry. Every day, 80,000 colleagues lead the way to greener and smarter mobility worldwide, connecting cities as we reduce carbon and replace cars. Could you be the full-time onsite Project Industrial Manager in New Castle, DE, US we're looking for? Your future role Take on a new challenge and apply your comprehensive industrial management expertise in a new cutting-edge field. You'll work alongside dedicated, innovative, and collaborative teammates. You'll ensure the robust application of industrialization processes and standards for maintenance, renovation/modernization, or warranty activity at the Depot, Repair Centre, or Production site(s) to secure production deliverables. Day-to-day, you'll work closely wit

NEW REK!! Job Title :CQV Engineer Location: Pennington, NJ Duration: Long term contract Responsibilities Develop and execute CQV protocols: Prepare commissioning, qualification, and validation documents for equipment, utilities, and systems. Perform system inspections and tests: Verify that systems and equipment operate according to design specifications and regulatory requirements. Document CQV activities: Prepare and maintain comprehensive validation documentation, including test protocols, reports, and standard operating procedures. Coordinate with cross-functional teams: Work closely with engineering, quality assurance, and production teams to resolve issues related to CQV. Monitor system performance: Implement corrective actions and improvements to maintain compliance with regulatory standards. Ensure compliance: Stay updated on industry regulations and standards related to CQV and ensure that all activities meet these requirements. Train staff: Conduct training sessions on CQV pr

Job Description Job Description The Food Safety Manager is responsible for overseeing the food safety program across the Company, ensuring compliance with local, state, and federal regulations, as well as company-specific policies. They will lead and supervise food safety practices, identify potential hazards, and create protocols to safeguard against contamination and ensure food quality. Key Responsibilities: Develop, implement, and maintain food safety policies and procedures in compliance with health and safety regulations (e.g., HACCP, FDA, USDA, OSHA). Monitor and enforce compliance with food safety standards throughout the food production or service process. Conduct regular inspections of food handling, storage, preparation, and sanitation practices to ensure food safety. Train and educate staff on food safety standards, including safe food handling, personal hygiene, and sanitation procedures. Respond to food safety emergencies, such as product recalls, contamination incidents,