Packaging Engineer
Baden-Wurttemberg
Contract
Negotiable
Research And Development
CR/551817_1751874736
Packaging Engineer
Job Title: Packaging Engineer - Medical Devices
Location: Germany (On-Site)
Contract Type: Freelance / Contract
Duration: 12 months (with potential extension)
Start Date: ASAP
About the Role:
We are seeking a highly skilled Packaging Engineer to support the development and validation of packaging solutions for Class III medical devices. This freelance role is ideal for an engineer with hands-on experience in packaging design, testing, and regulatory compliance-particularly within surgical devices, lab automation systems, or imaging technologies.
Important Requirements:
- Must have prior experience in the medical device industry. Applications without this experience will not be considered.
- Must have the right to work in Germany. Visa sponsorship is not available for this role.
Key Responsibilities:
- Design, develop, and validate packaging systems for Class III medical devices in compliance with ISO 11607 and other applicable standards
- Collaborate with cross-functional teams including R&D, manufacturing, and quality to ensure packaging meets product, user, and regulatory requirements
- Conduct packaging testing (e.g., transit, shelf-life, and sterile barrier integrity) and support documentation for regulatory submissions (e.g., CE marking, FDA)
- Support packaging process development, scale-up, and technology transfer to manufacturing
- Contribute to risk assessments, design reviews, and continuous improvement initiatives
Essential Skills & Experience:
- 5+ years of experience in packaging engineering within the medical device or life sciences industry
- Proven experience with medical devices and sterile packaging systems
- Strong understanding of packaging materials, sealing technologies, and validation protocols
- Experience with surgical instruments, lab automation systems, or diagnostic imaging products
- Familiarity with agile development environments and international project coordination
- Knowledge of EU MDR, FDA 21 CFR Part 820, and ISO 13485
- Excellent communication skills in German (required); English is a plus