Quality Assurance Engineer

🕒 Maio 1

🇺🇸 Estados Unidos – Remoto (EUA)

💵 $67.100 - $95.800 / ano

⏰ Tempo Integral

🟡 Pleno

🟠 Sênior

🔧 Engenheiro de QA (Qualidade de Software)

🦅 Patrocina Visto H1B

Esta empresa já patrocinou vistos H1B no passado.

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Covetrus

SiteLinkedInTodas as Vagas

5001 - 10000 funcionários

Fundada em 2018

⚕️ Seguro de Saúde

☁️ SaaS

🤝 B2B

💰 Seed Round em 2021-01

Healthcare Insurance • SaaS • B2B

A Covetrus é uma empresa global de saúde animal dedicada a apoiar veterinários e suas práticas. A empresa oferece um portfólio abrangente de software, suprimentos e serviços projetados para conectar o cuidado dentro e fora da clínica, focando na melhoria da saúde e bem-estar dos animais. Com forte ênfase em soluções tecnológicas, a Covetrus fornece software de gerenciamento de práticas, gestão de prescrições e várias ferramentas de engajamento do cliente para melhorar a eficiência operacional e o cuidado com os pacientes. Sua gama de soluções personalizadas de saúde para animais de estimação ajuda a impulsionar a conformidade, a eficiência e a rentabilidade das práticas veterinárias em todo o mundo.

Descrição

• Identify and prioritize opportunities to automate manual, repetitive, or error-prone processes across quality and regulatory workflows. • Leverage modern tools (e.g., AI assistants such as Copilot, ChatGPT, Claude; low-code platforms such as Power Automate) to design and implement practical automation solutions that improve efficiency, accuracy, and scalability. • Administer and optimize Quality Management Systems (QMS), electronic documentation systems, and integrated quality platforms to ensure data integrity, systems reliability, and regulatory compliance. • Develop, maintain, and enhance dashboards, automated workflows, and data analytics tools to monitor quality metrics, identify trends, and enable proactive decision-making. • Collaborate with IT and cross-functional teams to implement system integrations, automation solutions, and digital enhancements that improve QMS processes, quality operations and scalability. • Support and enhance day-to-day applicable QRO processes by applying engineering principles and technical solutions to ensure compliance with regulatory requirements and internal standards. • Work to identify opportunities and develop solutions to improve complex investigations related to complaints, Nonconformance Events (NCE), and CAPA, incorporating data analysis, root cause analysis tools, and system-based insights. • Drive improvements in quality processes related to Recall management systems and traceability, Supplier quality systems and performance monitoring, Drug Supply Chain Security Act (DSCSA) compliance systems and data exchange, and In-Clinic new item approval workflows and system enablement. • Ensure quality systems and electronic records comply with SOPs, regulatory requirements, and data integrity standards (e.g., ALCOA+ principles). • Design and maintain standardized documentation frameworks within QMS and related systems to ensure accuracy, traceability, and audit readiness. • Identify systemic risks, data inconsistencies, and process gaps; implement technical controls and automated solutions to mitigate quality and compliance risks. • Support internal audits, regulatory inspections, and system validations by providing technical expertise and ensuring system readiness compliance. • Identify opportunities for process implementation of continuous improvement initiatives. • Collaborate with QRO leadership, IT, Supply Chain, and other cross-functional teams to design and implement scalable quality solutions. • Provide technical guidance and training to team members on quality systems, automated processes, tools, and data utilization. • Complete all required training in accordance with established timelines. • Perform all other duties assigned to support quality and business objectives.

🎯 Requisitos

• Bachelor’s degree in a related field: Engineering, Computer Science, Information Systems, Chemistry, Biology, Pharmacy, Supply Chain or similar technical discipline. • Minimum 3-5 years of experience in quality engineering, quality systems, or a related technical quality role within pharmaceuticals, healthcare, or regulated environments; or equivalent combination of education and experience. • Demonstrated ability to use modern productivity and AI tools (e.g., Copilot, ChatGPT, Claude) to analyze data, streamline workflows, and accelerate problem-solving. • Strong technical writing skills with the ability to interpret complex data and translate insights into actionable improvements. • Experience with or strong interest in low-code/no-code automation tools (e.g., Power Automate or similar). • Strong curiosity and continuous improvement mindset, with a willingness to experiment with new technologies and approaches to enhance quality systems and processes. • Ability to identify automation opportunities and translate them into actionable solutions, collaborating with technical teams where needed. • Strong collaboration skills, with the ability to work effectively across Quality, IT, Product, and Operations to implement scalable solutions. • Experience with Quality Management Systems (QMS), data analytics tools, and process automation platforms. • Experience with leveraging technology to drive process standardization and efficiency. • Working knowledge of Drug Supply Chain Security Act (DSCSA) and system-related compliance requirements. • Knowledge of data integrity principles and electronic system compliance.

🏖️ Benefícios

• 401k savings & company match • Paid time off • Paid holidays • Maternity leave • Parental leave • Military leave • Other leaves of absence • Health, dental, and vision benefits • Health savings accounts • Flexible spending accounts • Life & disability benefits • Identity theft protection • Pet insurance