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One of the factors that make this possible is the talent of the team of people who make up the cooperative.

At i+MED we look for the best talent, wherever you are, and we offer an environment that favors the development of your professional career.

OPEN SELECTION PROCESSES

R&D Researcher

At i+Med S.Coop., we are looking to recruit an R&D Researcher with a PhD in Chemistry or Pharmacy and demonstrable experience in the development and characterisation of materials for pharmaceutical and biomedical applications.


We are looking for someone with strong knowledge of materials synthesis and characterisation, formulation development, work with nanoparticles, polymers and hydrogels, and hands-on experience in R&D laboratory environments.


RESPONSIBILITIES

• Understand and follow the procedures and technical instructions applicable to the role.

• Participate in the planning and execution of research and development projects.

• Design, develop and optimise formulations and prototypes for pharmaceutical and biomedical applications.

• Carry out laboratory- and pilot-scale testing.

• Perform activities related to the synthesis, encapsulation and characterisation of materials and nanoparticles.

• Prepare and maintain the technical documentation associated with the developments carried out.

• Analyse and interpret experimental results and propose improvements or new lines of development.

• Collaborate in technology transfer processes towards production.

• Prepare technical reports for internal and external clients.


REQUIREMENTS

PhD in Chemistry or Pharmacy.

Hands-on experience in one or more of the following areas:

• Synthesis and characterisation of materials.

• Encapsulation and characterisation of nanoparticles.

• Development and characterisation of polymers and hydrogels.

• Development of formulations for pharmaceutical or biomedical applications.

• Good knowledge and routine use of physicochemical characterisation techniques and materials analysis.

• Based in Vitoria-Gasteiz or the surrounding area.

• Minimum B2 level English.


WE WILL PARTICULARLY VALUE

• Experience in applied research or product development in an industrial, pharmaceutical, biotechnology or technology-centre environment.

• Experience in controlled drug delivery systems.

• Scientific publications or participation in research projects related to nanoparticles, hydrogels or biomaterials.

• Experience in scale-up transfer from laboratory to pilot plant.


COMPETENCIES

• Analytical skills and results orientation.

• Organisation and planning.

• Initiative and autonomy.

• Ability to work in multidisciplinary teams.

• Proactivity and problem-solving skills.

R&D Business Developer Specialist

We are looking to recruit an R&D Business Developer Specialist to support the growth of new business opportunities and the management of strategic projects linked to R&D&I.


WHAT WILL YOUR MISSION BE?

To contribute to the development of new commercial opportunities and strategic collaborations, taking part in the end-to-end management of innovation projects and acting as a link between the technical team, the client and funding opportunities.


MAIN RESPONSIBILITIES

• Identify, develop and manage new business opportunities.

• Manage relationships with potential clients and follow up commercial opportunities.

• Coordinate and monitor R&D&I projects.

• Prepare technical and economic feasibility studies for new projects.

• Manage the full lifecycle of selected projects and clients, from opportunity identification through to execution.

• Take part in projects combining technical, commercial and funding aspects.

• Support the development of international contacts and the creation of new strategic collaborations.

• Support activities related to market intelligence, trend analysis and the management of strategic databases.

• Work closely with technical, commercial and innovation teams to drive new initiatives.


WHAT ARE WE LOOKING FOR?


ESSENTIAL REQUIREMENTS

• University degree in Engineering, Biotechnology, Chemistry, Pharmacy, Health Sciences or related fields.

• High level of English (minimum B2-C1).

• Ability to work effectively in technical and innovation environments.

• Based in Vitoria-Gasteiz or the surrounding area.

• Availability to travel nationally and internationally, depending on the needs of projects, clients and collaborations.


DESIRABLE

• Previous experience in R&D&I, innovation or technology business development environments.

• Knowledge of innovation project funding, grants or R&D programmes.

• Experience in managing multidisciplinary projects.

• Experience working with international clients, partners or collaborators.

• Knowledge of market analysis and competitive intelligence.


KNOWLEDGE AND COMPETENCIES

• Ability to understand and communicate technical concepts.

• Strong organisational skills and ability to manage multiple projects simultaneously.

• Results orientation and business-development mindset.

• Analytical ability to assess opportunities and feasibility studies.

• Excellent communication and interpersonal skills.

• Proactivity, autonomy and ability to work in dynamic environments.

• High level of English (minimum B2-C1).

Regulatory Affairs Technician (RA)

We are looking for a Regulatory Affairs Technician (RA) to drive regulatory compliance in new developments focused on medical devices.


This position is key to ensuring that our innovative solutions reach the market safely and effectively while meeting all applicable regulatory standards.


RESPONSIBILITIES

• Develop technical documentation in accordance with Regulation (EU) 2017/745 (MDR) and other applicable regulations in the field of electromedical devices.

• Design and implement regulatory strategies (roadmaps) for new products, particularly electronic products, including certification routes, technical requirements and estimated timelines.

• Carry out regulatory feasibility studies for new concepts or product lines, identifying key risks and requirements.

• Conduct critical and continuous reviews of regulations and technical guidance, keeping the team up to date on relevant regulatory changes.


EDUCATION

University degree in a scientific or technical field, such as:

• Biotechnology

• Pharmacy

• Chemistry

• Biochemistry

• Industrial Engineering or similar

• Other related degrees


REQUIREMENTS

• Previous experience in regulatory affairs for medical devices.

• Knowledge of European regulations (MDR), ISO 13485 and Notified Body requirements.

• Experience in developing regulatory strategies.

• Ability to analyse scientific data and translate it into clear regulatory requirements.

• Fluent English, written and spoken, essential for documentation and communication with external organisations.

• Proactivity, critical thinking and results orientation.


EXPERIENCE

• Medical-device development.

• Participation in projects under ISO 13485.

Quality Assurance Technician

At i+Med, a leading technology cooperative in the development of medical devices, cosmetics and nutraceuticals, we are looking for a Quality Assurance Technician with solid experience in maintaining regulatory certifications and a practical, solution-oriented approach.


MAIN RESPONSIBILITIES

• Maintain and update quality management systems in accordance with:

• ISO 13485 (medical devices)

• ISO 22716 (cosmetics)

• Requirements applicable to food supplements and animal-health regulations.

• Prepare, coordinate and support internal, external and certification audits.

• Draft, review and control quality-system documentation (procedures, instructions, records, technical reports, etc.) and optimise systems.

• Carry out fieldwork in production and laboratory areas to:

• Identify incidents.

• Design effective and sustainable resolution strategies.

• Implement corrective and preventive actions.

• Monitor and analyse non-conformities, deviations and quality indicators.

• Coordinate change control and ensure documentary and operational traceability.

• Drive continuous-improvement initiatives and process-optimisation projects (5S, Lean, CAPA, etc.).


PROFILE REQUIREMENTS

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

• At least 2 years’ experience in quality departments within a regulated environment.

• Knowledge and experience of quality systems under ISO 13485, ISO 22716 for cosmetics, food supplements and animal-health regulations.

• Proactive profile, with critical thinking and a strong focus on solving problems on the production floor.

• Knowledge of continuous-improvement tools and root-cause analysis.

• Ability to work autonomously and in an organised manner, with a cross-functional perspective.

• Fluent English, written and spoken, essential for documentation and communication with external organisations.

GRAPHIC DESIGNER & ARTWORK SPECIALIST

FUNCTIONS AND RESPONSIBILITIES

• Design and develop graphic and communication materials for medical devices, cosmetics and food supplements, including catalogues, brochures, business cards, certificates, mock-ups, cartons, boxes, labels, instructions for use (IFU) and other packaging elements.

• Create graphic concepts and develop designs from scratch, adapting them to the brand’s visual identity, product needs and the requirements of each project.

• Develop and adapt packaging designs, preparing visual proposals, mock-ups and prototypes to validate their appearance and functionality before manufacture.

• Prepare, review and finalise artwork for print, ensuring that files meet the technical requirements needed for correct production.

• Review the technical aspects of final artwork, including margins, ink management, image resolution, typography, overprinting and adaptation to dielines.

• Check file dimensions, formats and technical specifications, as well as their suitability for the materials and printing systems defined by suppliers.

• Manage corrections and modifications to designs and final artwork, ensuring version control and correct file updates.

• Coordinate with printers, packaging manufacturers and other suppliers to resolve technical queries, review print proofs and ensure the correct reproduction of designs.

• Collaborate with Marketing, Quality, Regulatory and Production departments to ensure that graphic materials meet all applicable visual, technical and regulatory requirements.

• Keep project graphic documentation organised and up to date, including editable files, final artwork, dielines, specifications and approved versions.


QUALIFICATION REQUIREMENTS

• Higher education in Graphic Design, Graphic Arts, Graphic Production or a related field.

• Previous experience in graphic design and preparation of final artwork for print.

• Previous experience in printing, prepress, graphic production or packaging companies.

• Proficiency in Adobe Illustrator, InDesign and Photoshop.

• Strong knowledge of prepress, including colour management, inks, colour profiles, bleed, margins, dielines and preparation of files for print.

• Experience in the design and layout of corporate, editorial and commercial materials, as well as packaging and packaging development.

• Ability to work both on creative design and on the technical review and finalisation of files for production.

• Autonomy, organisation, attention to detail and ability to manage several projects simultaneously.


OTHER DESIRABLE KNOWLEDGE AND EXPERIENCE

• Experience designing cartons, boxes, labels and other materials for physical products.

• Experience in the pharmaceutical, medical-device, cosmetics or food-supplement sectors.

• Knowledge of labelling requirements and change management for regulated graphic materials.

• Knowledge of AI tools for image creation (Magnific, ChatGPT, Copilot, etc.).

• Interest in developing a professional career in the pharmaceutical and healthcare sector.

• Based in Vitoria-Gasteiz or the surrounding area, or willing to relocate to the area.

Spontaneous candidacy

What profiles are we looking for?

researchers specialized in encapsulation systems. Engineers Experts in the pharmaceutical industry processes. REGULATORY Experience in registration of medical devices

more information

Area of interest requerido

PDF, Word or OpenDocument. Maximum 5 MB.

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