Usp Manufacturing Technician
3 days ago
Nava
Overview We are looking for a results-driven, enthusiastic and proactive Upstream Technician to join our Manufacturing Operations Department. This role involves GMP-compliant biopharmaceutical manufacturing activities, process development support, and collaboration across departments to ensure high-quality production of biologics. No espere a enviar su solicitud después de leer esta descripción; se espera un gran volumen de candidaturas para esta oportunidad. Responsibilities • Ensure timely compliance with the planning of the USP Scale-Up and Manufacturing department as previously established by the Team Leader., • Provide proper training for personnel in charge., • Prepare, control and develop processes for production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Participate in internal and external audits as required by the Quality Assurance Department., • Comply with GMP standards within the work team and maintain documentation of quality indicators related to scale-up and manufacturing processes; participate in investigations with the Team Leader USP (FAB)., • Investigate and propose new methods or process innovations to optimize work in the area., • Ensure proper compliance with regulations and correct completion of current documentation., • Support transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and their manager., • Input documentation for new equipment in the USP Scale-Up and Manufacturing area under supervision, and supervise correct completion of entry documentation., • Supervise training of personnel as required and manage daily activity distribution., • Write and maintain documentation for production processes in the USP area., • Monitor orders in the USP production area using ERP software.Education and Experience, • Education: Bachelor's degree in Pharmacy, Biology, Biochemistry, Biotechnology, Chemistry, IPPA, Chemical Engineering, cell culture, or related fields. A Master’s degree or equivalent is desirable but not required., • Languages: Fluent in Spanish; intermediate English (B2 / First Certificate)., • Experience: 1–2 years in GMP/GLP environments with industrial-scale bioreactors, cell cultures, microbiological analysis techniques, upstream production positions, biotechnology or biopharmaceutical sectors.Other Requirements, • Open to work in shifts., • Software: Office (user level).Why 3P Biovian, • A permanent and stable position in a competitive growing company., • A competitive time-off package with 41 paid vacation days., • Flexible compensation plan allowing up to 30% of gross annual salary for eligible services (e.g., childcare, health insurance, academic training)., • Relocation assistance for new hires residing outside Navarra., • Company benefits club with exclusive prices and discounts on a wide range of products and services., • Commitment to continuous learning with a Learning Development department providing career plans., • Focus on internal talent, upskilling and reskilling, and opportunities for professional growth in a trustworthy environment., • Programs supporting well-being and participation in solidarity events and healthy workplace initiatives.Why us? We manufacture advanced medicines with a focus on process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. xcskxlj We support our clients from development to product delivery as a leading global CDMO and preferred partner in biotechnology. We are committed to helping our employees grow with us. #J-18808-Ljbffr