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Position Details
Summary
This job will be responsible to implement and coordinate the processes and the design for our packaging of our sterile medical tube sets and create reliable standards for future projects. Design, specification and the documentation in accordance to the MDR and all internal quality processes is accompanied from the start of development to serial production.
Primary Responsibilities
Development and modifications of packaging concepts and palletizing schemes for sterile medical devices.
Development and maintenance of a library of existing packaging materials and categorization of their performance levels
Specification, technical presentation and documentation of packaging variants for the packaging stages from product to pallet
Correspondence with project management, system architecture and the various production sites
Central contact person at the company site for packaging issues
Conducting feasibility analyses for the use of new packaging materials / packaging concepts
Execution of "Design to Cost" and "Design to Manufacturing" analyses
Establish test plans for packaging tests in early phases of product development
Coordination and evaluation of packaging tests
Accompanying the design transfer from development to series production
General Tasks
Strict compliance with the quality, occupational safety and environmental regulations.
Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist.
Required Experience, Education, Skills, Training and Competencies
Technical degree or completed technical training in the field of "Packaging engineering"
Professional experience in the field of packaging / packaging materials in medical technology
Good knowledge of the requirements of ISO 13485, ISO 9001 and MDR
High technical understanding and good communication skills
Good skills in spoken and written English
IT user skills and confident handling of common office programs
Good SAP knowledge
Good Creo knowledge (or a similar CAD 3D program)
Self-motivated, independent and structured way of working
Travel Requirements
Willingness to travel to suppliers or the production sites
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Novanta is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy.
Please call if you need a disability accommodation for any part of the employment process.
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