Osypka Medtec Jobs in United States

As a Manufacturing Engineer you will play a crucial role in the development and manufacturing of Class III medical devices. · ...

Production Supervisor · This is a full-time exempt benefited position that is responsible for overseeing production operations of Class III medical devices. · This supervisor will be in charge of ensuring that the production process is carried out efficiently and effectively, mee ...

This is a full-time exempt benefited position that oversees weekend production operations of Class III medical devices ensuring efficient and effective production meeting all quality standards and product specifications. · Monitor and manage the production process from start to f ...

HR Generalist · The HR Generalist serves as administrator for several critical human resources functions and workforce management, including recruiting, employee relations, benefits, employee engagement, leave and attendance tracking, and maintaining accurate employee records. · ...

The IT Systems Administrator supports the IT department at Osypka Medtec in Germany by ensuring smooth and efficient computer systems through regular assessment and implementation of new systems software troubleshooting technology issues and supporting the team with technology pr ...

Production Technician III · The person in the production technician III position will be responsible for the assembly, testing, and documentation of our cutting-edge, class III medical devices. You will work closely with our production and engineering teams to ensure the highest ...

+This position plays a critical role in maintaining and improving the quality management system elements and monitoring and trending data in an ISO 13485:2016 / 21CFR Part 820 regulated environment producing Class II and Class III medical devices and products. · +Collaborate with ...

Description · Essential Job Functions:  · Working in partnership with project manager and the quality team, manage the daily execution of tasks related to specific device development and manufacturing projects. · Working within the Quality Management System, and in partnership w ...

Description · Quality Engineer · This position plays a critical role in maintaining and improving the quality management system elements and monitoring and trending data in an ISO 13485:2016 / 21CFR Part 820 regulated environment producing Class II and Class III medical devices a ...

+Sr. Quality Engineer is responsible for ensuring quality and compliance of our products in accordance with ISO and FDA regulations. · +Lead quality investigations, develop quality systems and procedures, design control remediation, process validations. · Mentor other members of ...

The HR Associate will perform clerical and administrative tasks to support HR operations and projects. · ...

Ensure that products meet all regulatory and quality standards for a Class II and Class III medical device development and manufacturing company. · Lead quality team personnel including: quality engineers, quality specialists, · & quality control inspectors. · ...

Description · The Quality Control Inspector is responsible for ensuring that our Class II and Class III medical devices meet all quality standards and regulations throughout the manufacturing process. This person will work closely with the production team and engineers to conduct ...

The Quality Control Inspector is responsible for ensuring that our Class II and Class III medical devices meet all quality standards and regulations throughout the manufacturing process. This person will work closely with the production team and engineers to conduct inspections, ...