Quality Control Laboratory Analyst

• You will have a competitive total compensation package.
• You will have opportunities for learning and professional development.
• You will be able to benefit from our work-life balance measures, backed by the Family-Responsible Company Certificate (EFR).
• You will have the opportunity to develop professionally in a unique environment next to the Pyrenees, combining a career in the pharmaceutical industry with an excellent quality of life.

This is where your work makes a difference.

At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

At Baxter, behind every analysis and every quality control, there is a purpose: to contribute to ensuring that the products we manufacture reach patients with the required levels of quality and safety.

We are looking for a Laboratory Analyst to join the Quality Control team in the Chemical Laboratory at our Sabiñánigo (Huesca) plant.

As a Laboratory Analyst, you will have an important role within our manufacturing process. You will be responsible for performing assigned physicochemical controls on raw materials, in-process product, and finished product, helping to guarantee the quality and conformity of the product at different stages of the production process.

• You will perform chemical and physicochemical analyses of raw materials, in-process product, and finished product, contributing to verifying that materials and products meet the quality requirements established in the various manufacturing phases.
• You will generate fundamental analytical information to control the process and verify product quality.
• You will prepare the materials, reagents, media, and equipment necessary for the analyses, ensuring that laboratory work can be carried out in a reliable, orderly manner and in accordance with established procedures.
• You will perform stability testing of manufactured solutions, contributing to the monitoring of their quality during the established period.
• You will use and check laboratory equipment and collaborate in its correct maintenance, helping to guarantee the reliability of the equipment necessary to perform instrumental analyses.
• You will record analyses and their results in accordance with Good Manufacturing Practices (GMP), ensuring rigorous and traceable documentation that contributes to compliance with quality and data integrity standards.

Ultimately, your work in the laboratory will be an essential part of the plant's Quality Control system, helping us ensure that every analyzed product meets the required standards before advancing in the manufacturing process.

• Availability to work morning, afternoon, and night shifts.