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.

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. We support our clients from development to product delivery as a leading integral CDMO and preferred partner in biotechnology. We are committed to helping our employees grow with us.

📌 Usp Manufacturing Technician (El Remediu)
🏢 3PBIOVIAN
📍 El Remediu