Descripción de la oferta
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. 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. Requirements Bachelor's or higher degree in Chemistry, Biochemistry, Biotechnology, Pharmacy, or a related life science field. Solid hands-on experience in 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
