Back to jobs
Job Description
Summary
This 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.
