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 general CDMO and preferred partner in biotechnology. We are committed to helping our employees grow with us.

#J-18808-Ljbffr

📌 Usp Manufacturing Technician (Nava)
🏢 3PBIOVIAN
📍 Nava