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The Project Manager coordinates product development according to customer needs, manages timelines and budgets, facilitates team communication, and ensures compliance with quality standards.

Oversee design quality through product/process qualification, validate engineering changes, and manage documentation. Collaborate with teams to implement solutions and risk management.

The Quality Systems Manager oversees the Quality Management System, ensuring compliance and managing quality initiatives across Nextern US sites.

The Sr Quality Engineer leads quality activities in manufacturing, executes validations, and collaborates with teams to ensure compliance and process improvements.

The Sr. Project Manager will lead project initiatives in the medical device sector, coordinating product development, managing timelines and budgets, ensuring regulatory compliance, and mentoring junior managers.

The Senior Systems Engineer develops electro-mechanical systems, oversees project requirements, facilitates technical discussions, and contributes to compliance documentation, focusing especially on medical devices.

Responsible for managing cross-functional activities in new product development, tracking schedules and budgets, coordinating with stakeholders, and ensuring compliance with ISO 13485 standards.

Support equipment installation, qualification, testing, and troubleshooting for new tooling and product transfers. Assist process development, validation, data collection, documentation, and continuous improvement activities in a manufacturing environment.

The Process Development Engineer analyzes specifications, improves manufacturing processes, designs tooling, and collaborates across teams for product development, ensuring quality compliance and efficiency in production.

The Process Development Engineer designs and optimizes manufacturing processes, ensuring compliance with standards while managing projects and improving production efficiency.