POSITION SUMMARY: The Packaging Engineer will be responsible for management and execution of packaging design and manufacturing activities. The Packaging Engineer develops sterile and non-sterile packaging systems, manages technical aspects of packaging contract manufacturing, and develops packaging manufacturing systems.PRIMARY DUTIES AND RESPONSIBILITIES: Coordinates and monitors packaging projects and programs from inception through implementation. Establishes appropriate project schedules and prepares project reports periodically to outline progress. Applies knowledge of packaging materials, manufacturing methodologies, sterilization compatibility, and the distribution environment hazards to sustain and develop sterile barrier packaging solutions that meet medical device design requirements to our product portfolio. Specifies and develops packaging equipment and tooling for sterile packaging manufacturing. Drafts and executes Installation, Operation, and Performance Qualifications. Design/re-design package components and develop sterile and non-sterile packaging systems for new and existing medical device products with limited supervision. Defines applicable testing protocols and coordinates appropriate package and sterilization testing as required. Responsible for writing, reviewing, and approving of protocols and reports (internal and external). Interface with R&D, manufacturing, marketing, quality, and regulatory personnel to ensure user needs are met as well as compliance with Treace Medical Concepts Quality System requirements and FDA regulations. Develops engineering drawings for sterile and nonsterile package designs as required utilizing company CAD system (SolidWorks), and reviews final engineering drawings prior to approval. Develops material specifications for package components, prepares manufacturing process specifications for appropriate packaging processes, and responsible for change control activities and coordinating with sterile kit packagers- technical review of all the documentation sent/reviewed for MAPs, FMEAs, etc. Creates all Bill of Materials, Coordinate Instrument Case development activities, and generate Engineering Change Orders, packaging/labeling specifications and other technical packaging documentation for products. Coordinates with Regulatory Affairs and Quality on the requirements for package inserts, procedures, testing for packages and/or packaging materials, & labeling
