Packaging Engineer II (12 month contract // Memphis, TN):
Hybrid - Onsite at least 3 days per week
Top Skills:
CREO drawing software.
Sterile Packaging / Medical Device Packaging development, including knowledge of ISO 11607 and ISTA / ASTM standards
Project Management skills, including MS Project timelines and design history file management (file organization).
High level of Quality and Documentation/Reporting skills.
Education Required: Bachelors degree in Engineering field
Years' Experience Required: 2-5 years of packaging experience
Position Description:
This position supports sterile and non-sterile Packaging Development for Spine and Biologics product lines. This position is focused on Packaging Development for a site transfer project. Standard work for this role includes ensuring all testing meets the ISO 11607 requirements, updating package assembly prints, and updating Design History File documentation.
Duties:
Responsible for ensuring EU MDR Guidelines are met, and suggest where remediation steps may be needed.
Update existing files to meet state of the art file expectations Designs, develops, and tests a wide variety of containers used for the protection, display, and handling of products.
Determines packaging specifications according to the nature of the product, cost limitations, legal requirements, and the type of protection required, considering need for resistance to such external variables as moisture, corrosive chemicals, temperature variations, light, heat, rough handling, and tampering.
Designs package exteriors considering such factors as product identification, sales appeal, aesthetic quality, printing, and production techniques.
Responsibilities may include documentation management and/or coordination of Good Manufacturing Practices (GMPs) and may support prototype line development in manufacturing facilities/plants.