Ofertas de empleo de biologo

Buscamos a analistas para nuestro departamento de Microbiología.

Las principales responsabilidades son:

• Dar soporte en el control microbiológico.
• Análisis microbiológico de materias primas y productos acabados.
• Muestreo y análisis de aguas.
• Ensayos de endotoxinas por método Gel Clot y método LAL
• Ensayo de crecimiento microbiano en medios de cultivo.
• Dar soporte a los análisis en la preparación de muestras y en el uso de diversas técnicas analíticas.
• Realizar el trabajo en un entorno de cumplimiento de GLP y GMP

We are looking for analysts for our Microbiology Department.

Main responsibilities are:

• Support the microbiological control.
• Microbiological analysis of raw materials and finished products.
• Water sampling and analysis.
• Endotoxin assays by Gel Clot method and LAL method.
• Microbial growth assay in culture media.
• Support analysis in sample preparation and the use of various analytical techniques.
• Perform work in a GLP and GMP compliance environment.

We are recruiting an outstanding candidate to participate in a project funded by international and national institutions. Funding is already available for one year (initial gross salary range 24,000-27,000€ depending on experience).

You will join our laboratory of Translational Research in Neuromuscular Diseases at the Institut de Recerca Sant Joan de Déu, Hospital Sant Joan de Déu in Barcelona.
Our Institute is a leading biomedical research hub in Europe for rare diseases and one of the largest pediatric Hospitals in the world. We are a multidisciplinary group recognized as a reference centre for neuromuscular diseases working with an extensive network of collaborators inside and outside Europe. We participate in several clinical trials for various neuromuscular and neurological conditions.

The main functions of the candidate will be to carry out experiments related to the project, in particular those related to cell cultures, protein co-immunoprecipitation, nucleic acid extraction techniques, PCR, etc. In addition, you will have the responsibility of managing the results and issuing reports on them. The candidate will attend periodic meetings of the group and the research unit, where the results will be communicated and discussed critically.

Para importante instituto de patología dermahistológica y patología molecular en la ciudad de Friburgo, Alemania, TTA Personal selecciona un técnico en Anatomía Patológica y Citodiagnóstico (m/f)

Los laboratorios fueron fundados en 1992 y se han establecido como una referencia importante en la comunidad de Baden-Württemberg, Alemania y a nivel internacional. El objetivo de trabajo desde la fundación de la unidad de laboratorio ha sido ofrecer una histología contemporánea, moderna y comprensible. Los hallazgos actualmente están clasificados y ofrecen un diagnóstico lo más específico posible en el contexto de la clínica. Para ello se trabaja desde la recepción del tejido hasta el envío de los hallazgos. Este proceso suele tener lugar el mismo día. La compañía lleva más de un cuarto de siglo optimizando flujos de trabajo para poder brindar un diagnóstico adecuado en un tiempo breve. El laboratorio solo utiliza energía sostenible. Todos los dispositivos están sujetos a mantenimiento constante y se mantienen actualizados. El instituto en Freiburg se amplió para incluir una sucursal oficial en Teningen, que se especializa en los campos de citología y biología molecular.

Buscamos un técnico que trabajará en un equipo internacional para realizar la pruebas de tejido en sus diferentes pasos; recepción, teñido, cortes, deshidrataciones, incrustaciones en parafina, etc.. Trabajarán en unos modernos laboratorios con la última tecnología moderna con métodos innovadores.

Que se ofrece:

• Un contrato estable en unos laboratorios punteros
• Un excelente ambiente laboral en un ambiente internacional
• Un atractivo pago acorde a la experiencias y conocimientos del idioma alemán. Debes traer al menos conocimientos básicos. Sueldos para principiantes de 2.200-2.500€ brutos mensuales.
• Trabajo en jornada completa de 40h semanales
• 30 días laborable de vacaciones, 6 semanas
• Con un buen trabajo, salario 13 tras un año de empleo
• Día de entrevista y prueba con viaje y alojamiento pagado por la empresa
• Formaciones continuas a cargo de la empresa
• Ayuda para la adquisición del primer alojamiento en la zona
• Posibilidad de financiación posteriores cursos de alemán a través de EURES, hasta 2.000€
• Posibilidad de financiación de mudanza, hasta 1.000€ a través de EURES

• Mantener los archivos de productos locales de acuerdo con los detalles de autorización registrados actuales de acuerdo con la legislación local y de la UE pertinente.
• Preparar y enviar presentaciones regulatorias con el apoyo de las operaciones regulatorias.
• Mantenga la etiqueta y el empaque del producto de acuerdo con los detalles de autorización registrados actuales de acuerdo con la legislación local y de la UE pertinente.
• Contribuir al cumplimiento de todos los requisitos reglamentarios (presentación de expedientes, implementación de nueva legislación nacional e internacional, implementación...). 

• Estudios grado universitario en farmacia, bilogía, química o ciencias de la salud. 
• Experiencia previa en asuntos regulatorios. 
• Inglés fluido.  

• Contrato temporal de 6 meses
• Salario a negociar según experiencia demostrada.
• Jornada completa de L-V
• Centro de trabajo: Feria de Madrid

We are looking for a talented and motivated pre-award manager specialized in proposal writing to join the International Pre-Award Unit at Fundació Sant Joan de Déu. This team provides full support to Principal Investigators of Sant Joan de Déu’s research and innovation ecosystems to secure European and International competitive funding through identification of project ideas, deep knowledge of the funding Ecosystem and preparation of project proposals.

The position

The candidate will be in charge of co-developing successful research and innovation proposals with the PIs, to be submitted to European Commission-funded programmes. The final objective of this position is to maximize the value of the projects submitted in terms of research outputs, outcomes and impact. This position focuses on primarily on European Commission calls, ranging from Horizon Europe, EU4Health Programme, Erasmus+, CERV, among others, but also including other European and International public and private sources of funding such as US-NIH or private foundations.

Main tasks and responsibilities

• Knowledge on the interests and project portfolio of the Sant Joan de Déu’s research groups, oversighting its alignment with the trends of funding agencies.
• Comprehensive knowledge of European and international competitive funding programmes, relevant policies, and regulations, with a commitment to staying up to date.
• Identify and align research ideas with funding opportunities, ensuring that each project's concept meets the specific requirements and objectives of the call.
• Support the Principal Investigator with the structure and methodological design of the proposal.
• Write proposals covering Excellence, Impact, and Implementation, while collaborating closely with PIs to craft compelling research narratives that emphasize innovation, impact, and societal relevance.
• Conduct thorough reviews of proposal documents to ensure accuracy, completeness, and compliance.
• Support in the consortium building.
• Preparation of the budget including the management of the negotiation process with partners, including budget revisions, scope adjustments, and other matters.
• Stay informed about relevant trends, policies, and regulations in international development, grants management, and donor funding opportunities.
• Participate in lobby and networking opportunities.
• Organisation of information seminars for researchers.
• Contribute to the continuous improvement of pre-award processes, tools, and resources to enhance efficiency, effectiveness, and compliance.

GRUPO VALL COMPANYS

TECNICO/A CONTROL SALMONELLA

¿Quieres trabajar en un grupo empresarial líder en el sector agroalimentario europeo? ¿Te consideras una persona implicada, proactiva y comprometida, que trabaja bien en equipo? . Si es así, estás de suerte porque actualmente estamos buscando un/a TECNICO/A CONTROL SALMONELLA para una de nuestras empresas de la industria alimentaria ubicada en LLEIDA.

Sus funciones básicas consistirán en:

• Organizar y colaborar en el trabajo diario del Laboratorio de Salmonella para optimizar los recursos humanos y materiales disponibles.
• Supervisar los pedidos de compra relacionados con el laboratorio.
• Asumir la responsabilidad de las operaciones técnicas de la sección, incluyendo los análisis de microbiología acreditados por ISO 17025.
• Desarrollar y validar nuevos métodos de análisis relacionados con la seguridad alimentaria.
• Mantener la documentación cumpliendo con los requerimientos establecidos en los procedimientos de calidad.
• Etc

We are looking for a Scientist for our Biologics Quality Control Department.

Under the supervision of the Department Manager, the Scientist will be responsible for the following duties:

• The design, supervision and execution of quality control studies of Biological Products including chromatography and HPLC. At least 3 years of experience with these techniques is required.
• The management of the assigned projects keeping the deadlines and establishing a direct communication with the client
• Technical document management associated with the studies ( standard procedures, certificates of analysis, deviations, OOS’s, CAPA’s, etc.)
• The direction and supervision of the experimental work of the technical staff in charge.

• Puesto estratégico|Potencial de crecimiento

A recognized international company in the biotechnology R&D sector, specialized in the discovery of new natural products and biomarkers, requires the incorporation of Business Developer Manager (H/M/D), to take charge of international business development.

* Contribute and develop the network of contacts in the pharmaceutical/agro/cosmetics/biotechnology industry in the field of research or R&D. * Conduct prospecting, pre-sales, and develop proposals in response to the research and product development needs of each client. * Preparation of commercial reports. * Sales promotion and achievement of objectives. * Development of personalized methodology and commercial proposal for each project. * Participation in international trade fairs.

Professional carreer

• Multinational Company|Career development opportunity

Multinational company specialized in health supplements and bio ingredients

Reporting to the Regulatory Affairs Director, the Regulatory Affairs Specialist will be primarily responsible for:

• The preparation, submission, monitoring and updating of regulatory dossiers
• Prepare high quality regulatory dossiers (novel food, enzymes, GRAS, etc.) needed for the marketing of our products or those of our business partners in different territories, in compliance with relevant regulations and guidance documents.
• Prepare responses to questions from authorities resulting from the submission of the regulatory dossiers.
• Communicate with various internal stakeholders (R&D, quality assurance, etc.), for the collection of information necessary to complete regulatory files and responses.
• Submit documentation to the corresponding platforms of the Food Authorities (Health Canada, EU Commission FDA others), when needed.
• Perform data audit and gap analysis to understand which studies, tests and data are needed for regulatory approval and make reports accordingly.
• Participate in the recommendations for product regulatory positioning, risks, and opportunities.
• Assist the Regulatory Director in building regulatory strategies and roadmaps with pathways, costing and timelines to market.
• Monitor changes in regulations and keep updated with guidance documents in the relevant countries.
• Collaborate with other members of the regulatory affairs team on global projects.
• Perform the regulatory check of claims, marketing messages in advertising, marketing material, technical documentation, videos, to ensure compliance with main regulations.
• Create various documents in Word, Excel and PowerPoint for internal presentations and meetings.
• Carry out the classification and updating of various documents and databases.

Solid career opportunities

• World reference company in quality|Permanent position as Product Assesor -Technical Assessor

You will be part of an important company with a global reference in quality.

As a member of our Medical Device team, you will not only manage a small team of globally based Product Assessors but also dive deep into the exciting world of Active Medical Devices.

• Conducting thorough technical documentation reviews and ensuring compliance with EU regulations and standards.
• Collaborating with cross-functional teams to increase efficiency and quality
• Perform training and present the training to others in company or externally as deemed necessary.
• Assist with technical queries and those related to sales within the Active Medical Devices field.

• Immediate incorporation
• Permanent position in a World reference company
• Continuous training by the company
• Attractive fixed + variable salary