Immunology Scientist

Kymos Group; Barcelona; Presencial; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A dynamic life sciences company in Barcelona seeks an Immunology Scientist to join their team. The successful candidate will conduct analytical method development and validation for biologic products and oversee laboratory work ensuring compliance with GMP regulations. A Bachelor's degree in Biochemistry or related science is required, along with hands-on experience in relevant techniques. They promote an inclusive culture and offer a flexible work environment with numerous benefits.

Servicios

Flexible Hours

Employee benefits platform

23 vacation days plus holidays

Fully stocked kitchen

Beautiful natural surroundings

Collaborative work environment

Formación

• Solid hands-on experience in analytical method development and validation for biologics.
• In-depth understanding of GMP and ICH guidelines relevant to analytical method validation.
• English level equivalent to Cambridge First Certificate (B2) or higher.

Responsabilidades

• Design and oversee analytical method development and validation studies.
• Lead and manage assigned development and validation projects.
• Draft, review, and manage technical documentation.

Conocimientos

Analytical method development

Cell-based techniques

ELISA techniques

Documentation skills

GMP compliance

Project management

Collaboration

Educación

Bachelor's degree in Biochemistry, Biotechnology, Pharmacy, or related field

Descripción del empleo

Immunology Scientist

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 an 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.

Requisitos

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.