R&D Analyst

CHEMO pharmaceutical group; León; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

Una empresa innovadora en el sector farmacéutico busca un Analista de I+D para realizar pruebas y validar métodos analíticos. En esta emocionante posición, serás responsable de asegurar la calidad y la conformidad de los productos farmacéuticos mediante la realización de pruebas rigurosas y el desarrollo de metodologías. Se valoran habilidades analíticas y una sólida comprensión de las regulaciones GMP. Este es un entorno dinámico donde tu contribución tendrá un impacto significativo en el desarrollo de productos de calidad. Si tienes pasión por la ciencia y el deseo de crecer en tu carrera, esta oportunidad es perfecta para ti.

Formación

• Mínimo 1-4 años de experiencia como analista en la industria farmacéutica.
• Conocimiento de las regulaciones GMP y técnicas analíticas.

Responsabilidades

• Realizar pruebas y validar métodos analíticos para productos farmacéuticos.
• Registrar resultados analíticos y producir informes con conclusiones.

Conocimientos

Habilidades analíticas

Confiabilidad

Paciencia

Educación

Estudios básicos en Análisis Químico

Herramientas

Cromatografía Líquida

Descripción del empleo

Chemo Villaquilambre, Castilla and Leon, Spain

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Overview
Perform tests for finish products, APIs, excipients, stress degradation, stability, pre-stability, trials, reference product and GMP batches. Perform development, validation and verification of analytical methods. Control and identify the samples in the chamber and in the laboratory.
Report the results and evaluate them with the specification.

Responsibilities

• Assign any sample with an ID according to the SOP to ensure sample traceability.
• Perform tests in developing, verify and validate analytical methods for API, excipients and Pharmaceutical Product Development R&D.
• Register the analytical results of the tests and produce reports with the results and conclusions.
• Inform the Analytical Development Scientist about the results obtained, and any incident occurring during the analysis.
• Propose changes and / or variations in analytical tests carried out to improve methodologies.
• Inform, investigate and document OOS and OOT in a timely manner.
• Calibrate if applicable and maintain R & D as per specific SOP. Review and maintain stock levels of materials, consumables, reagents (standard and other products).
• Advice, train, support and verify the work done by other analysts to ensure a good functioning and success of the department.
• Train the new incorporations in the specific activities and functions of the position in which you are an expert.

Competencies/Career level

Innovation, customer orientation, communication, teamwork, adaptability/flexibility, productivity, self-development, sense of urgency, initiative.

Accountabilities

KPI related to the job.

Qualifications

Requirements and personal skills

• Education: Basic Studies in Chemical Analysis.
• Languages: High level of Spanish and medium level of English.
• Experience (years/area): Minimum 1-4 years’ experience in the functions mentioned above as analyst in the pharma industry, working with drugs. Handling Equipment of Liquid Chromatography. Knowledge in other analytical techniques.
• Specific Knowledge: GMP regulations.
• Travels: Not required.
• Personal skills: Analytical skills, reliability and patience.

Seniority level

Not Applicable

Employment type

Full-time

Job function

Business Development and Sales

Industries

Pharmaceutical Manufacturing