Descripción de la oferta
We are looking for a results‑driven, enthusiastic and proactive Upstream Technician to join our Manufacturing Operations Department.
Main Responsibilities
Ensure timely compliance with the planning of the USP Scale‑Up and Manufacturing department previously made by a Team Leader.
Ensure the correct training of the personnel in charge.
Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms.
Participate in internal/external audits as required by the Quality Assurance Department.
Comply and ensure compliance with GMP standards within the work team.
Record and manage any quality indicators associated with a scale‑up and manufacturing process; participate in the investigation of the same together with the Team Leader USP (FAB).
Investigate and propose new methods or process innovations to optimize and improve the work in the area.
Ensure proper compliance with regulations and correct completion of current documentation.
Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and their manager.
Perform the entry documentation of new equipment from the USP Scale‑Up and Manufacturing area under the supervision of the Team Leader USP (FAB).
Supervise the correct completion of the new equipment entry documentation.
Supervise the correct training of the personnel in charge, if any.
Carry out the distribution and supervision of daily activities.
Write and keep updated the documentation associated with the production processes carried out in the USP area.
Control/monitoring of orders placed in the USP production area using ERP software.
Assessment Criteria
Education: Bachelor's degree in Pharmacy; Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, cell culture etc. Desirable but not required Master's degree or equivalent in related fields.
Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate).
Experience: Between 1 and 2 years of experience in/with:
GMP/GLP regulations
Industrial‑scale bioreactors
Cell cultures
Microbiological analysis techniques
Upstream production positions
Biotechnology / Biopharmaceutical sector
Other requirements: Open to work in shifts. Software package: Office. User level.
Benefits
Permanent and stable position in a growing company.
Competitive paid vacation: 41 days.
Flexible compensation plan allowing up to 30% of gross annual salary for daily services exempt from income taxes.
Relocation assistance for hires outside Navarra.
Company benefits club with exclusive prices and discounts on products and services.
Learning & Development department for personalized career plans.
Focus on internal talent, upskilling and reskilling, and professional growth opportunities.
Encouragement to participate in solidarity events and employee well‑being programs.
High‑impact work environment with flat hierarchies and short decision‑making processes.
USP Manufacturing Technician • Noáin, comunidad foral de Navarra, Spain
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