Scientist

Kymos Group; Cerdanyola del Vallés; Presencial; EUR 40.000 - 55.000; Jornada completa

Descripción de la vacante

A leading Biologics company is seeking a highly motivated Scientist to join their Biologics Team in Cerdanyola del Vallés, Spain. This role entails the design and execution of transfer studies and validations of Biological and Small Molecules products within a GMP-regulated environment. Required qualifications include a Bachelor's degree in a relevant field and hands-on experience with HPLC methods. An inspiring workplace surrounded by nature with flexible hours and various employee benefits is offered.

Servicios

Flexible hours

Employee benefits platform

23 vacation days

Fully stocked kitchen

Rooftop terrace with views

Formación

• Bachelor's or higher degree in a related life science field.
• Solid hands‑on experience in HPLC methods and Quality Control of Proteins.
• In-depth understanding of GMP requirements.

Responsabilidades

• Design, supervise, and execute transfer and validations studies.
• Lead and manage assigned projects while meeting deadlines.
• Draft, review, and manage technical documentation.

Conocimientos

HPLC methods

Chromatography

Quality Control of Proteins

Electrophoretic techniques

Western-Blot

ELISAs

Organizational skills

Documentation skills

Project management

English (B2)

Educación

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

Descripción del empleo

We are seeking a highly motivated Scientist to join our Biologics Team. This role, reporting to the Department Manager, focuses on the transfer studies of Biological products and validation of Small Molecules products in a GMP-regulated environment.

Key responsibilities

Design, supervision and execution of the transfer and validations studies of Biological and Small Molecules Products.

Hands‑on experience with techniques such as chromatography and HPLC.

Lead and manage assigned the assigned projects keeping the deadlines and establishing a direct communication with the client.

Draft, review, and manage technical documentation associated with the studies (protocols, reports, standard procedures, certificates of analysis, etc.).

Supervise and mentor laboratory analysts and technical staff during experimental work, promoting scientific excellence and GMP compliance.

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.

Requirements

Bachelor's or higher degree in Chemistry, Biochemistry, Biotechnology, Pharmacy, or a related life science field.

Solid hands‑on experience in HPLC methods, Quality Control of Proteins will be a plus.

In-depth understanding of GMP requirements

Experience with electrophoretic techniques, Western‑Blot and ELISAs 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.

We Value Diversity

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.