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Packaging Design Lead
2 months ago
At Eliassen Group, we are seeking a highly skilled Packaging Design Lead to join our team. As a key member of our design team, you will be responsible for designing and producing packaging/labeling for all new and existing products.
Key Responsibilities:- Design and Production: Designs and produces packaging/labeling for all new and existing products, ensuring compliance with domestic and international regulatory labeling requirements, Health Industry Barcode Communications Council requirements, and company standards for high-quality, accuracy, and cost efficiency.
- Conceptualization: Conceptualizes multi-lingual packaging/labeling symbols, colors, and graphics to create original, visually appealing, and competitive images and combinations in the marketplace.
- Documentation and Maintenance: Documents graphic design content requirements and production processes, creates, updates, and maintains labeling formats produced with in-house production printing systems.
- Product Database Management: Populates product databases for new and existing products.
- Compliance: Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
- Artwork Design: Designs artwork for product labeling (e.g., defines format/graphic requirements) by using departmental computer graphics software from input provided by Regulatory Affairs, Marketing, Engineering, and other departments.
- Packaging and Labeling Strategies: Recommends and contributes ideas of packaging and labeling strategies to project leaders by utilizing package labeling knowledge gained from historical data and material characteristics.
- Translation and Procurement: Procures foreign languages translations by forwarding English formatted text to translation agency and produces artwork packages for procurement for the Materials and Receiving Inspection Departments.
- Sample Label Preparation: Provides sample labels for filing submissions by printing requested labels.
- Change Order Preparation: Prepares Change Orders (COs) and specifications for approval by writing CO and specifications for CO originator to obtain approvals.
- Verification: Verifies COs are completed correctly prior to submission to Document Control Archiving by comparing signed CO to printed electronic version of CO.
- Professional Development: Keeps up-to-date on technological advances in the marketplace by attending classes/trade shows and reading trade journals.
- Education: Associate's degree or equivalent related experience to ensure basic skills and knowledge of the job requirements.
- Experience: Minimum of 4 years' experience in a quality or operational area, with knowledge of regulations and standards affecting 510(k), Class I, II, and III medical devices.
- Soft Skills: Must have capacity for attention to detail, ability to recognize errors in spelling, punctuation, and grammar, and ability to work independently as well as within a team.