Biopharmaceutical Scientist

Kymos Group; Barcelona; Presencial; EUR 42.000 - 65.000; Jornada completa

Descripción de la vacante

Kymos Group is seeking a highly motivated Scientist to join the Biopharmaceutical Analysis team in Barcelona. The role focuses on transfer studies of Biological products and validation of Small Molecules in a GMP-regulated environment, reporting to the Department Manager.

You will design and supervise transfer/validation studies, perform HPLC-based analyses, and manage project timelines with direct client communication while ensuring high-quality technical documentation and GMP adherence.

Formación

• Experience in transfer and validation studies for Biological and Small Molecules.
• Experience with GMP-compliant documentation and lab supervision.

Responsabilidades

• Design, supervise and execute transfer and validation studies of Biological and Small Molecules products.
• Hands-on experience with chromatography and HPLC.
• Lead and manage assigned projects, maintaining deadlines and client communication.
• Draft, review and manage technical documents (protocols, reports, SOPs, certificates of analysis).
• Supervise and mentor laboratory analysts and technical staff, ensuring GMP compliance.

Conocimientos

Biopharm analysis

HPLC

Chromatography

Project leadership

GMP compliance

Herramientas

HPLC instrumentation

Descripción del empleo

We are seeking a highly motivated Scientist to join our Biopharmaceutical Analysis 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.