**About us** ------------------ We are an industrial company **leading internationally in the field of biotechnology and advanced therapies, based in Donostia\-San Sebastián, with a major expansion project, an unwavering passion for science, and a commitment to excellence and people.** Our **purpose:** improving people's lives through revolutionary advances in biotechnology and gene therapy that cure rare diseases and cancers. With a philosophy of not only working together but growing together, our client's culture is based on honesty, excellence, leadership, involvement, ethics, and rigor. We are a **CDMO** (Contract Development and Manufacturing Organization) and **the trust placed in us by more than 40 biotechnology companies worldwide is our best endorsement.** We develop and manufacture viral vectors (lentiviral), being one of the European leaders operating in accordance with EMA and FDA regulations. Lentiviruses produced by VIVEbiotech are used for the treatment of various diseases including hematological and solid cancers, or rare diseases. **We are looking for you to join our Team!** ### **Your role** We are seeking **Production Technicians** to perform this key function reporting directly to the Production Manager (USP/DSP). **You will carry out lentiviral vector production processes according to manufacturing guideline instructions under GMP regulations.** To achieve this, you will be part of a team where you will propose improvements, draft manufacturing protocols, standard operating procedures (SOPs), and other relevant documentation related to manufacturing. ### **Your responsibilities** * Carry out lentiviral vector production processes according to manufacturing guideline instructions under GMP regulations. * Draft manufacturing protocols, standard operating procedures (SOPs), and other relevant manufacturing-related documents. * Comply with and ensure compliance with internal production standards. * Be part of a multidisciplinary team to conduct process optimizations and investigations. * Perform maintenance of production areas to ensure their condition and compliance with GMP regulations. ### **What we value in you** You are who we are looking for if you have: * A degree related to biomedical research (Sciences, Biology, Biochemistry, Chemistry, Pharmacy…) or related engineering. * Higher-level qualification related to the field. * Previous experience in production within GMP environments and/or bioprocesses will be positively valued. * Ability to suggest potential process improvements and tests. * Competent verbal and written communication skills in Spanish and English. * Ability to work in a team and meet deadlines. * Residence in Gipuzkoa (or intention to relocate to the area) will be positively considered. ### **We offer you** * You will have continuous career development opportunities that will help you grow your talent throughout your professional journey. * You will participate in innovative projects with constant technological updates. * You will receive a competitive salary commensurate with your profile for this position. * You will become part of an expert, young, dynamic, innovative, and enthusiastic team united by a common purpose: supporting our clients in advancing cures for diseases. * We will support you during your personal relocation process if you come from another region and wish to move to Donostia\-San Sebastián (accommodation, job placement for family members, school enrollment, ...). * You will enjoy a professional work environment that truly stands out due to our humanity and closeness, where we care about diversity and inclusion. Diverse perspectives and your curiosity bring varied capabilities that strengthen our approach and drive our growth. * We take pride in offering equal opportunities. All individuals receive equal consideration for our open positions, regardless of gender, age, race, religion, identity, sexual orientation, origin, disability, or any other characteristic.