Research Associate III - ICP-OES/MS Lead

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.

At Baxter Healthcare, we are dedicated to enhancing the quality of life for people around the world. As part of our analytical team, we are seeking a highly skilled and experienced Research Associate III - ICP-OES/MS Lead to manage a team of SMEs working in the laboratory on specific ICP-OES/MS techniques.

In this role, you will be responsible for planning and supervising ICP-OES/MS analytical method development and optimization on raw materials and finished products, with support from technical SMEs. You will collect relevant information related to product specifications and propose appropriate analytical methods, define and propose validation/transfer designs, ensure testing follow-up, and communicate results.

What you'll be doing :

• Manage a team of analytical SMEs on ICP-OES/MS techniques
• Plan and supervise method development and optimization on raw materials and finished products
• Collect relevant product information and propose appropriate analytical methods
• Define and propose validation/transfer design, ensure testing follow-up and communication of results
• Order required materials and equipment for studies
• Write/review comprehensive protocols and reports in English
• Lead method evaluation, validation, or transfer (Baxter or CRO)
• Provide advice and assistance to team members
• Interpret experimental data and present conclusions to project leader and management
• Work with applicable software and statistical tools
• Review data and results critically for compliance with protocol and procedures
• Lead investigation on failed acceptance criteria
• Adhere to quality system requirements, GMP, GDP and EHS guidelines
• Create and update equipment and analytical procedures
• Independently make decisions and propose activities for potential questions from authorities
• Contribute to innovative ideas for improvement

What you'll bring :

• Master or PhD or strong equivalent expertise in relevant Sciences Domain
• 5 years of experience in analytical chemistry, method development/Validation
• Knowledge of new analytical strategies as described in ICH Q14 (QbD)
• Strong technical knowledge in ICP-MS/ICP-OES, with experience in managing method development, validation, transfer, and investigation
• In-depth understanding of GxP and related regulations and guidances
• Previous experience in project management, with knowledge of interactions with other fields (formulation, regulatory affairs, process development, quality control, manufacturing, etc.)
• Able to make critical decisions, solve issues, and develop solutions with "out of the box" thinking
• Able to lead a small team, mentor junior associates, and communicate sophisticated information effectively
• Strong written and oral communication skills, proficiency in English

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

We offer a competitive 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.

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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