Company Description

LVD Biotech - iVascular Group is an international medical technology group specializing in the development, manufacturing, marketing and distribution of innovative medical devices for the treatment of vascular diseases worldwide. Our vertically integrated business model enables us to manage the entire product lifecycle, from innovation and development to manufacturing and commercialization.

The Group comprises two highly specialized and complementary companies:

- LVD Biotech, our innovation center, leads and drives research and development of new technologies, managing the entire product development cycle from the initial concept through to the preparation of regulatory dossiers. This includes generating, developing and protecting knowledge through intellectual property.
- iVascular transforms this innovation into medical solutions that reach healthcare professionals and patients through the manufacturing, logistics, marketing and international commercialization of a portfolio of medical devices across the Coronary, Peripheral and Neurovascular fields.

With a team of more than 600 professionals and a commercial presence in over 86 countries, both companies work closely together in an environment of continuous collaboration, combining science, innovation, industrial excellence and the highest quality standards.

Together, we drive the development of cutting-edge medical solutions with a shared goal: improving patients’ quality of life worldwide.

Position

We are currently looking for a QUALITY ENGINEER to join the Quality team at our plants located in Sant Vicenç dels Horts, Barcelona.





Your main objective will be to ensure that the safety and quality of our products meet the required quality standards and requirements before being released to the market. To do so, you will assess, develop and implement preventive quality measures, in-process controls, process robustness improvements and raw material controls. As a key part of the role, you will also monitor and analyse production and field incidents and data in order to identify and resolve issues in the most agile and effective way.

DUTIES AND RESPONSIBILITIES

- Product quality issue and non-conformity management: Ensure they are handled in accordance with requirements, lead investigations, identify root causes and define corrective and preventive actions (CAPA).
- Risk analysis: Participate in process FMEAs, design reviews and risk assessments related to non-conformities.
- Quality plans: Ensure the correct implementation of product quality plans, process parameters and raw material requirements.
- Materials and suppliers: Assess raw material non-conformities, analyse supplier responses and collaborate in audits.
- Equipment and processes: Review and approve qualifications and validations, and propose improvements to equipment, tools and procedures.
- Quality system: Collaborate in the effective implementation of the quality system, internal audits, document control, traceability and regulatory compliance.




- You will interact internally with all departments, as well as externally with health authorities, official bodies, certification bodies, suppliers and customers.

Requirements

DESIRED PROFILE

- University degree, preferably a Bachelor’s degree or Engineering degree.
- Training and experience in ISO 13485, MDR, MDSAP and 21 CFR.
- More than 5 years’ experience in a similar position, preferably in the medical device, healthcare products, automotive, metallurgical or mechanical-electronic industry as a Quality and/or Production Engineer.
- High level of written and spoken English. An English level test will be carried out.
- Analytical, proactive, problem-solving, rigorous and organised person, with strong communication and interpersonal skills, as well as strong leadership capabilities.

Benefits

Health Insurance Flexible working hours On-the-job training Language courses Career progression opportunities Free On-Site Gym Subsidised meals Company events / Team-building activities

Other information

WHAT WE OFFER

- Permanent and stable contract in a project with high global impact and expanding internationally.
- Professional and personal development in a vibrant, dynamic, and youthful environment.
- Competitive salary tailored to your experience, along with an attractive benefits package.
- Adaptable working hours to support a healthy work-life balance.
- Flexible compensation (meal vouchers, transportation, and childcare assistance).
- Access to our iWellness program: gym and physiotherapist on site.
- Corporate events and gifts.
- Subsidized on-site company cafeteria.

Apply for this job

📌 Quality Engineer (España)
🏢 iVascular
📍 España