The Packaging Engineer II is responsible for the design, development, validation, and implementation of packaging systems that protect products through distribution, storage, and use. This role contributes to packaging projects of moderate complexity, supporting design, validation, and commercialization activities within a regulated medical device manufacturing environment.
Key Duties and Responsibilities
Support design and development of packaging systems (materials, components, and processes) to meet product, regulatory, and business requirements
Execute packaging validation activities including protocol development and testing support (IQ/OQ/PQ), ensuring compliance with applicable standards and quality systems
Perform packaging testing and analysis (e.g., transit testing, seal strength, aging) to evaluate performance and integrity
Support new product introduction (NPI) and packaging changes by coordinating trials, documentation, and process readiness for manufacturing
Troubleshoot packaging processes and equipment on the production floor, working with Operations and Maintenance to resolve issues and improve performance
Develop and maintain packaging documentation including specifications, work instructions, and validation reports to support design control and change management
Collaborate cross-functionally with Quality, Manufacturing, Supply Chain, Regulatory, and external suppliers to deliver project objectives
Support material and supplier evaluations, including testing, qualification activities, and cost/quality optimization
Contribute to continuous improvement initiatives focused on cost reduction, efficiency, and quality enhancement
Job Requirements
Bachelor’s degree in Engineering or related discipline
2+ years of packaging engineering experience in a manufacturing or regulated environment
Preferred Experience
Knowledge of packaging materials and processes (sealing, labeling, inspection)
Exposure to validation methodologies (IQ/OQ/PQ) and design control processes
Strong problem-solving and analytical skills
Ability to manage multiple projects with moderate direction
Effective cross-functional collaboration
Ability to support shop-floor trials, testing, and equipment implementation as needed
Experience in medical device or other regulated industry
Exposure to: Packaging validation and test methods (ASTM/ISTA, as applicable) Statistical analysis tools (e.g., Minitab)
Experience with packaging equipment and automation
Familiarity with ISO 11607 and applicable regulatory standards and Engineering or manufacturing systems (ERP/MES)
Expected Travel 0-20%
This position is not eligible for employer-visa sponsorship
This job posting is anticipated to close on June 26, 2026. We may, however, extend this time period, in which case the posting will remain available on careers.conmed.com. Please submit your application as soon as possible as we will be reviewing applications on a rolling basis as we receive them.
Benefits:
CONMED offers a wide array of benefits to fit your unique needs. Visit our Benefits Page for more information.
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CONMED is an equal opportunity employer and does not discriminate on the basis of any legally protected status or characteristic. Protected veterans and individuals with disabilities are encouraged to apply. The Know Your Rights: Workplace Discrimination is Illegal Poster reaffirms this commitment.
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