Product Verification Lead

Introduction:

Based in Gembloux, Intressa Vascular is a clinical-stage company developing an innovative medical implant to address life-threatening cardiovascular conditions such as aortic dissection.

Our mission is to help physicians address the devastating effect of aortic dissection by delivering next-generation endovascular treatment.

To strengthen our team, we are looking for a Product Verification Lead to play a key role in ensuring our development activities meet the highest quality and regulatory standards.

Job purpose:

Reporting to the Operations Director, the Product Verification Lead is responsible for confirming that development outcomes fully satisfy defined technical requirements. This is achieved through rigorous testing, inspections, reviews, and demonstrations throughout the product development cycle.

Duties and Responsibilities:

He/She is responsible, in a proactive and results-driven manner to:

- Identify, qualify, and oversee subcontracted laboratories; ensure testing schedules, specifications, and results meet contractual and regulatory expectations.

- Establish and maintain incoming, in-process, and final product inspections; define control plans, protocols, and inspection methods to ensure product compliance.

- Develop and implement verification strategies and test protocols aligned with ISO and regulatory standards; contribute to risk analysis and industrialization planning.

- Act as a key quality liaison during external testing and industrialization phases; ensure effective use and calibration of control and measurement tools.

- Author and maintain quality system documentation; manage traceability and archiving of inspection records, certificates, and batch files.

- Compile and provide documentation required for internal and external audits by notified bodies, customers, and suppliers.

Profile:

- Industrial or Civil Engineer in the fields of Mechanics, Electromechanics or Biomechanics.

- 5 years of relevant experience in an industrial environment, in the medical device (preferred).

- Strong knowledge and understanding of risk management and quality management system principles (ideally ISO 13485 – ISO 9001 – GMP/GLP).

- Knowledge and practice of product design control and process validation according to medical device regulation (EU and USA).

- Roll-up-your-sleeves attitude, autonomous and hands-on mindset

- Excellent communication skills (written and verbally) and strong problem-solving abilities.

- High level of attention to detail, excellent organizational skills and time management.

- Fluent in French and English, written and spoken.

Our offer:

- A challenging and diversified position within a high-potential innovative medical device company.

- A human-sized, collaborative, and respectful work environment.

- An attractive compensation package in line with the position responsibilities and your experience.