Ofertas de empleo en Kymos Group

• Flexibilidad horariaSí
• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• PublicadaNueva

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We are hiring a Scientist for our Percutaneous Absorption department.

Under the supervision of the Department Manager, the Scientist will carry out the following activities:

• Conduct in vitro release studies of dermal/topical products from the development to the final stages.
• Perform in vitro permeation studies through biological membranes from the development to the final stages.
• Be responsible and accountable for the execution and oversight of the assigned IVRT/IVPT projects.
• Preparation of study protocols and reports.
• Knowledge in the use of equipment for sample analysis generated from the in vitro studies, mainly HPLC.
• Equipment maintenance and qualification operations.
• Writing and update of specific Standard Operational Procedures of the department.
• Ensuring compliance with timelines and quality of the studies.
• Work under GLP/GMP standards.
  
  
  

• Degree in chemistry, biotechnology, pharmacy or biology.
• Experience in transdermal or in semi-solid products.
• In depth knowledge in working in a GLP/GMP environment.
• Able to work and lead studies autonomously.
• Good communication and interpersonal skills.
• Good planning, organization and problem-solving activities.
• Proactive, adaptable and energetic approach.
• English – Level B2.
  
  
  

• Working in a dynamic company with a highly qualified growing team
• Professional development and collaborative environment and a culture of empowerment.
• Flexible Working Hours.
• Access to the employee benefits flexibility platform.
• 23 vacation days per year plus 24th and 31th of December.
• Fully stocked canteen and rooftop space (coffee, fruits, snacks, and beverages).
• Our headquarters located in Cerdanyola del Vallés, an amazing place at the foothill of Collserola Park, the green lung of Barcelona, with our Rooftop terrace.
  
  
  

• Flexibilidad horariaSí
• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada15 ene.

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Estamos contratando un Revisor de Calidad Interno para nuestro Departamento de Control de Calidad de Biológicos. El revisor será responsable de las siguientes funciones:

• Revisar auditar los datos primarios del departamento procedentes de estudios GMP.
• Colaborar en la mejora interna de procesos de registro de datos
• Tareas administrativas generales (gestión de laboratorio, archivo de documentación, recepción de muestras)
  
  
  

• Ciclo formativo Análisis Químico, Control de calidad, Auxiliar de farmacia, Análisis clínico o similar
• El candidato debe tener conocimientos de Técnicas de Control de Calidad y Análisis en Productos Farmacéuticos y de la normativa GMP.
• Para este puesto se requiere un nivel medio de inglés escrito
  
  
  

• Trabajar en una empresa dinámica con un equipo en crecimiento altamente cualificado
• Desarrollo profesional y entorno colaborativo y una cultura de empoderamiento.
• Horario flexible y horario intensivo los viernes.
• Trabajo híbrido, pero principalmente en la oficina.
• Acceso a la plataforma de flexibilidad de beneficios para empleados.
• 23 días de vacaciones al año más los días 24 y 31 de diciembre.
• Comedor completamente abastecido y espacio en la azotea (café, frutas, bocadillos y bebidas).
• Nuestra sede se encuentra en Cerdanyola del Vallès, un lugar increíble a los pies del Parque de Collserola, el pulmón verde de Barcelona, con nuestra terraza en la azotea.
  
  
  

• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada8 ene.

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We are seeking a highly motivated Scientist to join our Biologics and Advanced Therapies Quality Control team. This role, reporting to the Department Manager, focuses on the analysis of biological products in a GMP-regulated environment.

Key responsibilities:

• Design, execution, and oversee of analytical method development and validation studies for biologic products, including monoclonal antibodies, recombinant proteins, and advanced therapies.
• Hands-on experience with techniques such as HPLC, capillary electrophoresis, ELISA, protein quantification (e.g., BCA, UV), and other relevant biochemical methods.
• Lead and manage assigned development and validation projects, ensuring timely execution, compliance with regulatory requirements, and effective communication with internal and external stakeholders.
• Draft, review, and manage technical documentation including method validation protocols and reports, SOPs, risk assessments, and technical justifications.
• Collaborate with cross-functional teams including Quality Assurance and Marketing to support method development and validation.
• Supervise and mentor laboratory analysts and technical staff during experimental work, promoting scientific excellence and GMP compliance.
  
  
  

• Bachelor's or higher degree in Biochemistry, Biotechnology, Pharmacy, or a related life science field.
• Solid hands-on experience in analytical method development and validation for biologics, particularly using HPLC, capillary electrophoresis, and immunoassay-based techniques.
• In-depth understanding of GMP requirements and ICH guidelines relevant to analytical method validation.
• Experience with HPLC and Capillary electrophoresis development will be considered a strong asset.
• Excellent organizational and documentation skills, with the ability to manage multiple projects simultaneously.
• English level equivalent to Cambridge First Certificate (B2) or higher.