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Laboratory Analyst (AMD)

Publicada el 15 de Mayo de 2026

Noáin (Valle de Elorz)/Noain (Elortzibar)

Descripción

Main Responsibilities:

As a Laboratory Assistant of the AMD laboratory facilities, your responsibilities will include:

  • Execute method analyses required to support the production processes executed both in process development and in plant under non-GMP conditions. Analytical analyses that may include both process control samples and final product (DS) and/or finished product (DP).
  • Execute analytical analyses necessary for the development, implementation, qualification and transfer of analytical methods and collaboration with the technician in the treatment of the results obtained.
  • Execute the analyses included in stability studies, forced degradation studies, characterization of reference materials, research and other studies that are not included in the previous descriptions.
  • Execute verification and calibration actions of equipment associated to the analysis as required.
  • Carry out stock management of reagents and materials commonly used in the laboratory.
  • Manage internal and customer reference materials.
  • Collaborate with the auxiliary team in the correct handling, recording and storage of process samples and retention samples.
  • Report results via database or required documentation in AMD according to current procedure to ensure traceability.
  • Prepare reagents, solutions and culture media required in AMD Bio and control their stock.
  • To be responsible for the compliance and follow-up of the established procedures (SOPs) for each specific analysis and of the requirements and deadlines established for their execution.
  • Contribute to the drafting of SOPs.
  • Support in the training of other 3P staff members.


Why 3PBiovian?

  • A permanent and stable position in a competitive growing company.
  • A competitive time off package with 41 paid days of vacation.
  • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.)
  • All new hires who reside outside Navarra are provided with a relocation service and/or assistance.
  • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.)
  • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees.
  • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust.
  • We encourage the participation of our employees in solidarity events such as charity races, social donations...
  • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces.
  • We have a high-impact work environment with flat hierarchies and short decision-making processes.

...And so much more!

It´s within us.

Requisitos mínimos

Assessment criteria:

Education

  • Higher Level Training Cycle related to the area (Clinical Analysis and Quality Control Laboratory; Laboratory Analysis; Chemistry, etc).
  • Valuable but not essential University Degree or equivalent related to the area (Chemistry; Biochemistry; Biotechnology; Biology, etc.).
  • Valuable, but not essential Master's Degree or equivalent related to the area (Chemistry; Biochemistry; Biotechnology; Biology, etc.).


Languages

  • Fluent in Spanish.
  • Intermediate level of English (Level B2 / First Certificate) is desirable.


At least 1 year of experience in/with:

  • Biopharmaceutical or biotechnology sector.
  • Analytical methods such as: SDS-PAGE; Western-Blot; Determination of total protein concentration; ELISA; qPCR; Capillary Electrophoresis and other biochemical techniques.
  • Participation in research projects is valuable, but not required.
  • Knowledge of GMP environments is valuable, but not necessary.


Other requirements

  • GMP training is valued.