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R&D Specialist – Injectable Medical Devices | ISO 13485 Environment
Rieka Talent —Castelló d'Empúries, Girona provincia
- Jornada completa
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- Español
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Cementos Molins —Girona, Girona provincia
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- Español
- Presencial
- Formación continua
- Flexibilidad horaria
Copilot Studio Consultant (m/f/d)
Zoi —Figueres, Girona provincia
- Jornada completa
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- Inglés
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14d
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Business Process Manager
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- Microsoft Excel
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11d
Associate in Fund Accounting
Fundcraft —Girona, Girona provincia
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Zoi —Figueres, Girona provincia
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TÉCNICO/A PRL - INDUSTRIAL
Talent Services —Girona, Girona provincia
- De 35.000 € a 42.000 € al año
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Gestion del Cambio Empresarial —Girona, Girona provincia
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Cloud Partnership Development Manager (m/f/d)
Zoi —Figueres, Girona provincia
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KPMG Abogados Girona —Girona, Girona provincia
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9d

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R&D Specialist – Injectable Medical Devices | ISO 13485 Environment

Rieka Talent
Castelló d'Empúries, Girona provincia

Solicitud rápida

Detalles del empleo

Contrato indefinido | Jornada completa

Cualificaciones

ESO
Español
Inglés
Máster
Química
Gestión del ciclo de vida del producto

Descripción completa del empleo

DESCRIPTION

At Rieka Talent, we are currently searching for an R&D Specialist on behalf of one of our clients, an innovative company operating in the pharmaceutical and medical devices sector, based in Castelló d'Empúries (Girona, Spain).

Position Objective

The R&D Specialist will be responsible for the development and improvement of analytical methods and techniques for the characterization of injectable medical devices, while supporting product development projects from concept through commercialization.

The successful candidate will lead hands-on analytical development activities, apply advanced characterization techniques, solve technical challenges related to product development, and generate scientific data to support innovation, regulatory compliance, and business objectives.

Working closely with cross-functional teams, the R&D Specialist will contribute to the development of innovative, robust, and compliant products while providing scientific and technical expertise across the organization.

Key Responsibilities

1. Analytical Method Development & Material Characterization

Develop and validate analytical methods in accordance with ICH Q2 guidelines.
Characterize cosmetics and medical devices using techniques such as rheology, texture analysis, microscopy, particle characterization, titrations, HPLC, UV-Vis, and other analytical methodologies.
Collaborate with external laboratories and partners when required.
Prepare validation protocols, plans, and reports.

2. Medical Device Development

Develop new injectable medical devices in compliance with ISO 13485 requirements.
Maintain, improve, and manage the lifecycle of existing products.
Generate and review technical documentation, procedures, and work instructions related to design and development activities.
Support product development from concept to market launch.

3. Scientific & Technical Support

Design and execute analytical and performance studies.
Investigate technical issues and implement corrective actions.
Evaluate emerging technologies, materials, and scientific literature to support innovation initiatives.
Manage technical interactions with external laboratories, suppliers, consultants, and partners.
Prepare technical documentation supporting regulatory compliance and product lifecycle management.
Provide scientific support to Regulatory Affairs, Quality Assurance, Marketing, Operations, and other departments.
Contribute to scientific publications and patent applications.

Key Performance Indicators (KPIs)

Successful delivery of analytical and performance studies meeting project objectives and quality standards.
Execution of product development activities according to project timelines and ISO 13485 requirements.
Timely completion of technical documentation in compliance with quality and regulatory standards.
Effective resolution of technical investigations and implementation of corrective actions.
Publication of scientific papers in peer-reviewed journals.

What We Offer

Opportunity to join an innovative and growing company within the pharmaceutical and medical devices industry.
Participation in cutting-edge R&D projects focused on injectable medical devices.
International and multidisciplinary working environment.
Competitive compensation package according to experience and qualifications (around 45,000€ gross annual salary).
Flexible working schedule.
1 day of remote work per week (hybrid model).

If you are interested in this opportunity or would like to learn more, please contact Rieka Talent for a confidential discussion.

REQUIREMENTS

Ideal Candidate Profile

Education

Master's Degree in Chemistry or a related scientific discipline.

Experience

Proven experience in analytical method development and validation, Research & Development, Product Development, or related scientific roles within a regulated environment.
Strong background in data interpretation, technical documentation, and scientific reporting.
Hands-on experience with analytical techniques including HPLC, UV-Vis, titrations, rheology, texture analysis, microscopy, and statistical analysis.
Experience in medical devices, drug delivery systems, injectable products, aesthetics, or dermatology will be highly valued.
Knowledge of medical device design and development under ISO 13485 standards is considered a strong advantage.

Languages

Fluent English, both written and spoken (mandatory).
Spanish and/or another European language is a plus.

Solicitud rápida

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