Research Associate II - ICP-OES and MS

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

We are seeking a dedicated Research Associate with expertise in ICP-OES/MS techniques to join our dynamic team in Braine L'Alleud.

In this role, you will be responsible for developing, evaluating, and validating analytical methods using ICP-OES/MS techniques for products under development.

You will craft experiments, perform testing, and demonstrate strong analytical skills to run 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 with expertise in ICP-OES and ICP-MS techniques, you will be responsible for collecting information required for the analytical target profile for method development.

You will perform feasibility, development, and validation/transfer of analytical methods on raw materials and finished products, with a focus on ICP-OES and ICP-MS methods, including methods for elemental impurities determination.

Your role will also involve providing support for initiatives in technological development, competitive product analysis, market and regulatory affairs questions, industrial troubleshooting, and other projects.

You will apply current physical, chemical, and physicochemical techniques in accordance with GMP and local procedures, and record your results according to established GDP procedures.

Interpret experimental data and present your conclusions to supervisors, project leaders, and management.

Adhere to the quality system requirements and ensure GMP and GDP standards, as well as 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 external partners and take ownership to follow up on project progression.

In addition, 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 :

• Minimum bachelor degree with 5 years of related experience or advanced degree

• Relevant laboratory/technical, writing, and computer skills

• Analytical Chemistry: knowledge of ICP-OES & ICP-MS analytical techniques and Good Laboratory Practices (GLP)

• Experience on trace chemical analysis

• Good technical knowledge on ICP-OES/MS techniques with previous experience on development, validations, or investigation on analytical methods

• Proficiency in English

• Operates in certified environments by aligning with quality systems in place

• Objective assessment, organization, and clear communication of sophisticated information

• Critical thinker and “out of the box” thinking to identify and solve technical issues

• Ownership for getting the job done, presenting with supervision and customers when facing issues, and proposing options to meet timelines or define new timelines

• Driven for results

• Team environment and inclusive attitude

• Appropriate prioritization of assignments to meet project schedules and demonstrates flexibility

What are some of the benefits of working at Baxter Healthcare Corporation?

We offer a driven total compensation package, with professional development opportunities, where a high importance is placed on work-life balance!

Equal Opportunity Employer Statement: Baxter Healthcare Corporation is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Reasonable Accommodation Statement: Baxter Healthcare Corporation is committed to providing reasonable accommodations to applicants with disabilities. If you require a reasonable accommodation during the application process, please let us know.

If you are a proactive, analytically-minded professional with a strong background in ICP-OES/MS techniques, we encourage you to apply for this exciting opportunity. Join us in our mission to drive growth and advancement in the field of research and development!

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

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