Usp Manufacturing Technician
hace 2 días
Asturias
ph3Overview /h3pWe 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. /ph3Responsibilities /h3ulliEnsure timely compliance with the planning of the USP Scale-Up and Manufacturing department as previously established by the Team Leader. /liliProvide proper training for personnel in charge. /liliPrepare, control and develop processes for production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms. /liliParticipate in internal and external audits as required by the Quality Assurance Department. /liliComply 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). /liliInvestigate and propose new methods or process innovations to optimize work in the area. /liliEnsure proper compliance with regulations and correct completion of current documentation. /liliSupport transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and their manager. /liliInput documentation for new equipment in the USP Scale-Up and Manufacturing area under supervision, and supervise correct completion of entry documentation. /liliSupervise training of personnel as required and manage daily activity distribution. /liliWrite and maintain documentation for production processes in the USP area. /liliMonitor orders in the USP production area using ERP software. /li /ulh3Education and Experience /h3ulliEducation: 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. /liliLanguages: Fluent in Spanish; intermediate English (B2 / First Certificate). /liliExperience: 1–2 years in GMP/GLP environments with industrial-scale bioreactors, cell cultures, microbiological analysis techniques, upstream production positions, biotechnology or biopharmaceutical sectors. /li /ulh3Other Requirements /h3ulliOpen to work in shifts. /liliSoftware: Office (user level). /li /ulh3Why 3P Biovian /h3ulliA permanent and stable position in a competitive growing company. /liliA competitive time-off package with 41 paid vacation days. /liliFlexible compensation plan allowing up to 30% of gross annual salary for eligible services (e.g., childcare, health insurance, academic training). /liliRelocation assistance for new hires residing outside Navarra. /liliCompany benefits club with exclusive prices and discounts on a wide range of products and services. /liliCommitment to continuous learning with a Learning Development department providing career plans. /liliFocus on internal talent, upskilling and reskilling, and opportunities for professional growth in a trustworthy environment. /liliPrograms supporting well-being and participation in solidarity events and healthy workplace initiatives. /li /ulh3Why us? /h3pWe manufacture advanced medicines with a focus on process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. 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. /p /p #J-18808-Ljbffr
Polígono Baíña Industrial, 33682, Asturias
