Osypka Medtec Jobs in United States

The IT Systems Administrator's main responsibility is to ensure smooth and efficient computer systems through regular assessment of existing technology, identifying areas for improvement, and implementation of new systems and software. This role is also responsible for troublesho ...

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. · ...

The inventory control clerk III is responsible for managing and maintaining accurate inventory levels of parts, components, and tools used in the development and manufacture of Class III medical devices. · This role plays a critical part in maintaining an efficient and cost-effec ...

+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 ...

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

+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 ...

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 ...

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 ...

This is a full-time exempt benefited position that oversees weekend production operations of Class III medical devices. · $75,000 to $95,000 Annually, Depending Upon Qualifications · ...

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.Paid Vacation · ...