Biosafety Engineer: Medical Devices & Sterilization

AMjobcenter; Heverlee; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

Materialise Medical is seeking a professional to support biocompatibility evaluations and validate cleaning, packaging, and sterilization processes for medical devices. You will coordinate with testing labs, manage sample production with manufacturing and suppliers, and contribute to regulatory submissions.

Join a team focused on patient safety and regulatory excellence, acting as a safety ambassador and collaborating across Quality, Regulatory, Development, and Manufacturing to ensure compliant

Qualifikationen

• Master degree in engineering, biochemistry, biology or medical field.
• Strong understanding of regulatory requirements in biocompatibility evaluation, cleaning validation, packaging development or sterilization validation.
• Ability to work on multiple projects simultaneously and set priorities.
• Independent decision-making with team collaboration.
• Clear and effective verbal communication and technical writing in English.
• Strong analytical skills and meticulous attention to detail.

Aufgaben

• Support biocompatibility evaluations in accordance with ISO 10993-1.
• Develop and validate cleaning, packaging, and sterilization processes.
• Contribute to validation protocols and reports; ensure clarity and compliance.
• Coordinate tests with external labs and manage sample production with manufacturing and suppliers.
• Interact with internal stakeholders and external partners to ensure smooth collaboration.
• Act as ambassador for biological safety within Materialise Medical and safeguard safety measures.

Ausbildung

Master degree in engineering/biochemistry/biology/medical

Jobbeschreibung

Materialise Medical is seeking a professional to support biocompatibility evaluations and validate cleaning, packaging, and sterilization processes for medical devices. You will coordinate with testing labs, manage sample production with manufacturing and suppliers, and contribute to regulatory submissions.

Join a team focused on patient safety and regulatory excellence, acting as a safety ambassador and collaborating across Quality, Regulatory, Development, and Manufacturing to ensure compliant