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

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