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Immunology Scientist

Trabajo disponible en: 08001, Barcelona, Cataluna, España
Empresa: Kymos Group
Tiempo completo puesto
Publicado en 2026-02-12
Especializaciones laborales:
  • Servicios Médicos
    Ciencia Médica
  • Investigación/Desarrollo
    Investigador científico, Ciencia Médica
Rango Salarial o Referencia de la Industria: 30000 - 50000 EUR Anual EUR 30000.00 50000.00 YEAR
Descripción del trabajo

KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain (Cerdanyola del Vallés
- Barcelona), Italy (Monsano-Ancona), and Germany (Frankfurt) and a Liasson office in South Korea (Seoul), offering comprehensive bioanalytical and CMC analytical services to the life sciences industry. Its laboratories are GMP and GLP certified and GCP compliant, and have been successfully inspected by EMA, FDA, and ANVISA.

KYMOS GROUP is devoted in providing high quality and added value services to its partners and it is highly oriented to innovation, offering services of research, development and quality control in many different fields such as small molecules, proteins, antibodies, nucleic acids, and advanced therapies.

KYMOS GROUP has a young and dynamic staff of more than 250 employees, and it is committed in promoting diversity, gender-equality, well-being, and initiative within its members, encouraging career development and internal promotion.

Due to our recent business expansion and facility growth, we are looking for an Immunology Scientist to join our dynamic team.

As Immunology Scientist, you will be part of our Immunology Bioassay team. This role, reporting to the Department Manager, focuses on the analysis of biological products in a GMP-regulated environment and your responsibilities will include.

  • Design, execution, and oversee of analytical method development and validation studies for biologic products, including monoclonal antibodies, recombinant proteins, and advanced therapies.
  • Experience in working in BSL-2 cell laboratories.
  • Hands‑on experience with cell based or ELISA techniques.
  • 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.

If you join us, you will become part of an agile and growing company with a strong scientific culture.

Here’s what you can expect:
  • A collaborative, empowering environment focused on continuous learning and professional growth.
  • Flexible Hours and intensive Fridays.
  • A Flexible employee benefits platform.
  • 23 vacation days per year + 24th and 31st of December as holidays.
  • A Fully stocked kitchen (Coffee, fruits, snacks, and beverages).
  • An inspiring workplace surrounded by nature- our headquarters located at the foot of Collserola Natural Park (Barcelona) with a Rooftop terrace and beautiful views.

Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic.

What we are looking for
  • 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 cell-based and immunoassay-based techniques.
  • In‑depth understanding of GMP requirements and ICH guidelines relevant to analytical method validation.
  • Excellent organizational and documentation skills, with the ability to manage multiple projects simultaneously.
  • English level equivalent to Cambridge First Certificate (B2) or higher.
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