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Quality Assurance Technician

On-site in Vitoria-Gasteiz·Full-time·Added 2 days ago

i+Med S.Coop.

3 open roles

Overview

Job details

  • Full-time hours

    Per the ad.

Requirements

  • Have the right to work in Spain

    i+Med S.Coop. doesn't mention sponsorship in the ad.

  • Work in English

    English is required, per the ad.

  • Work on-site in Vitoria-Gasteiz

    No relocation package mentioned.

  • Have 2+ years of experience

    Mid-level role.

  • University degree

    “Formación universitaria en áreas científicas o técnicas: Farmacia, Química, Biología, Ingeniería, etc.” — per the ad.

This job was automatically translated to English.

Requirements

What we're looking for

  • University degree in scientific or technical areas: Pharmacy, Chemistry, Biology, Engineering, etc.

  • Minimum of 2 years of experience in quality departments within a regulated environment.

  • Knowledge and experience in quality systems according to ISO 13485, ISO cosmetics (22716), food supplements, and zoosanitary regulations.

  • Proactive profile, withcritical capacity and problem-solving orientation in the plant.

  • Knowledge of continuous improvement tools and root cause analysis.

  • Ability to work autonomously, organized, and with a transversal vision.

  • Fluent English (written and spoken), indispensable for documentation and relationship with external entities.

The role

Ati+Med, a leading technological cooperative in the development of medical devices, cosmetics, and nutraceuticals, we are looking for aQuality Assurance Technician with solid experience inmaintaining regulatory certifications and with a practical and decisive profile.

What you'll do

  • Maintain and update quality management systems in accordance with regulations:

  • ISO 13485 (medical devices)

  • ISO 22716 (cosmetics)

  • Requirements applicable tofood supplements and zoosanitary regulation.

  • Prepare, coordinate, and provide support forinternal, external, and certification audits.

  • Draft, review, and control quality system documentation (procedures, instructions, records, technical reports...). System optimization.

  • Performfieldwork in the plant and laboratory to:

  • Detect incidents,

  • Design effective and sustainable resolution strategies,

  • Implement corrective and preventive actions.

  • Monitor and analyzenon-conformities, deviations, and quality indicators.

  • Coordinatechange control and guarantee documentary and operational traceability.

  • Drivecontinuous improvement initiatives and process optimization projects (5S, lean, CAPA, etc.).

How you'll work

Location: Vitoria-Gasteiz |Job type: Full-time |Modality: On-site

About i+Med S.Coop.

i+Med S.Coop. is a cooperative of scientists from the Basque Country that researches, develops, manufactures and commercializes high value-added pharma-sanitary products. It specializes in smart nanohydrogels and controlled-release systems for active ingredients, a technology backed by 14 patents, and operates as a CDMO offering third-party development and manufacturing services. The company reports 52 products on the market, 172 R&D projects and a team of more than 200 people, with 14 years in the pharma industry. Its portfolio covers human health areas (traumatology, aesthetics, ophthalmology, dermatology, women's health, oral care) and animal health, in forms such as injectable solutions, ophthalmic drops, oral formulations and topicals.

Industry
Medical Devices
Employees
200+
In Spain
Madrid

Good to know if you are moving

  • i+Med is a certified multi-site company, with cleanroom manufacturing and lab space in the BIC science park in addition to its main Vitoria-Gasteiz site.
  • The team counts more than 200 people, and the company reports 14 years in the pharma industry, 52 products on the market and 14 patents.
  • Current openings — quality assurance technician, supply chain, and international market sales representative — are all listed as on-site ('Presencial') in Vitoria-Gasteiz.
All open roles at i+Med S.Coop.
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