SummaryThis role is responsible for supporting the global packaging functions of the business, encompassing both sterile and non-sterile products. The position will contribute to packaging-related tasks aligned with the global strategy for revenue growth, profit growth, business continuity, as well as mergers and acquisitions. This is an on-site position located in Caledonia, MI, with travel required up to 25% of the time.
In This Position, You Will Have the Opportunity To- Execute packaging validations for new or existing products with compliance to ISO 11607 regulations.
- Assist in identifying cost-saving opportunities within current packaging configurations or processes.
- Adhere to project plans, tasks, and deliverables, effectively managing time to meet project deadlines.
- Participate in troubleshooting and problem-solving efforts related to development projects, supporting decisions through comprehensive engineering analysis and data.
- Assist in developing validated sealing processes for sterile barrier packaging.
- Support packaging process validation using various sterile packaging equipment.
- Remain current with industry technology and trends.
- Provide general technical assistance to various internal departments and individuals as needed for exploring new opportunities and resolving issues.
What You Need to Succeed in This Position- Bachelor's degree in Packaging Engineering or a related field.
- 5+ years of experience in packaging design and development.
- Experience in medical device design and development is preferred.
- Working knowledge of packaging equipment, including Form, Fill, Seal (FFS) machines, bar sealers, etc.
- Strong working knowledge of ISO 11607 and transit testing standards such as ASTM 4169 or similar.
- Demonstrated verbal & written communication skills, with the ability to lead within a cross-functional team.
- Familiarity with Risk Management methodologies and Failure Mode and Effects Analysis (FMEAs).
- Preferred knowledge and experience with TOPS or a similar system.
