Research Associate II - Numeta

Baxter International

Braine l'Alleud, Belgium

This is where you save and sustain lives

We are seeking a dedicated Research Associate to join our dynamic team in Braine L'alleud.

In this role, you will be responsible for developing, evaluating, and validating analytical methods using a range of techniques, including LC and titration, among others.

You will craft experiments, perform testing on products under development, and demonstrate a strong analytical competence to manage various projects and identify risks and opportunities for innovation.

This role will require a basic technical understanding of related fields, such as Product Development, Delivery Systems Development, Analytical Development, Quality Control, Process Development, and Manufacturing.

Collaboration and teamwork are essential, as you will be expected to participate in team projects and work closely with other R&D groups.

What you'll do

As a Research Associate, you will be responsible for capturing vital information for the analytical target profile from the project team, including analytical leads, project managers, and product owners;
You will develop, validate, and transfer analytical methods using conventional techniques such as LC, GC, UV, and titration for raw materials and finished products;
Your role will also involve providing support for initiatives in technological development, competitive product analysis, market and regulatory affairs questions, and industrial troubleshooting;
You will apply current physical, chemical, and physicochemical techniques in accordance with GMP and local procedures, and detail your results according to established GDP procedures;
Interpret experimental data and present your conclusions to supervisors, project leaders, and management;
Maintain laboratory reagents, materials, and equipment as advised, ensuring they are in good operating order;
Adhere to the quality system requirements, GMP and GDP standards, and general and specific environmental, health, and safety guidelines;
Write comprehensive protocols and reports in English, and participate in the update of analytical procedures;
When required, you will contact the appropriate parties to address any issues. Additionally, you will participate in investigations, change control impact assessments, and the preparation of risk assessment reports in accordance with pharmaceutical guidelines (USP, ICH, EP).

What you'll bring

Around Bachelor degree with 5 years of related experience or Master degree with 2-3 years of experience;
Relevant laboratory/technical, writing, and computer skills;
Analytical Chemistry: knowledge of conventional analytical techniques and Good Laboratory Practices (GLP);
Knowledge of Compendial and other regulations applicable to analytical activities within Pharmaceutical environment;
Good technical knowledge on various techniques with experience in development, validation, or investigation on analytical methods;
Fluency in English;
Operates in certified environments by aligning with quality systems in place;
Appropriate prioritization of assignments to meet project schedules and demonstrates flexibility;
Team environment and inclusive attitude;
Driven for results;
Ownership for getting the job done, communicating with supervision and customers when facing issues, and proposing options to meet timelines or define new timelines;
Critical mind and “out of the box” thinking to identify and solve technical issues;
Objective assessment, organization, and clear communication of complex information.