Senior Staff Packaging Engineer - 253169
Medix™
Job Description
Responsibilities:
\n- \n
- Lead packaging engineering activities for sterile and non-sterile medical devices throughout the product lifecycle. \n
- Develop, execute, and maintain packaging design verification and validation activities. \n
- Author and review packaging validation protocols and reports, including IQ, OQ, and PQ studies. \n
- Develop and execute transportation/shipping validation protocols and testing. \n
- Author and manage accelerated and real-time aging studies and associated documentation. \n
- Ensure compliance with ISO 11607 and applicable medical device packaging standards and regulations. \n
- Support design control activities, risk assessments, design changes, and product development projects. \n
- Collaborate with contract manufacturers, packaging suppliers, material vendors, and testing laboratories to develop and qualify packaging solutions. \n
- Evaluate packaging materials, specifications, and manufacturing processes to ensure product protection and regulatory compliance. \n
- Troubleshoot packaging-related issues and implement corrective actions when necessary. \n
- Contribute to the establishment and continuous improvement of packaging engineering processes, procedures, and documentation. \n
- Partner with Quality, Regulatory Affairs, Operations, Supply Chain, and R&D teams to support product launches and ongoing commercial products. \n
Qualifications:
\n- \n
- Bachelor's degree in Packaging Engineering, Engineering, Science, or related technical field. \n
- Minimum 6 years of medical device packaging engineering experience. \n
- Direct experience supporting Class I, II, and/or III medical devices. \n
- Experience with sterile and/or non-sterile packaging systems. \n
- Strong background in packaging design verification and validation. \n
- Hands-on experience developing and executing IQ, OQ, and PQ validation protocols. \n
- Experience authoring shipping and transportation validation protocols and reports. \n
- Experience developing and executing accelerated aging and shelf-life studies. \n
- Working knowledge of ISO 11607 requirements. \n
- Experience supporting design control processes and product development activities. \n
- Strong technical writing and documentation skills. \n
Vacancy posted 3 days ago
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