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Summary:
Form part of a group of technical experts (SMEs) responsible for the continuity, quality, compliance, and profitability of the on-market Clinical Nutrition (pharmaceutical) portfolio. Lead and support the execution of product changes in compliance with international regulations and quality standards, working with cross-functional teams to ensure effective problem-solving, decision-making, and timely change implementation. The position combines strong technical expertise, project leadership, and people management responsibilities, driving lifecycle management activities and operational excellence across regions.
Essential Duties and Responsibilities:
- Manage routine and complex changes for the on-market Clinical Nutrition (pharmaceutical) portfolio. Mentor/lead a team of scientists responsible for lifecycle design and change execution activities for on-market products. Provide direction on prioritization, technical problem solving, and process clarification, ensuring alignment with organizational objectives.
- Plan, organize and execute product changes in compliance with global regulatory and quality requirements. Lead cross-functional teams and facilitate decision-making to ensure timely project delivery.
- Apply advanced scientific and cross-functional knowledge to drive outcomes. Utilize project management tools to manage timelines, risks, and budgets, while identifying and resolving issues impacting delivery.
- Establish and maintain metrics to track operational performance and KPIs. Communicate progress and results to management and Senior Leadership Team (SLT) as required.
- Drive market enhancements and operational improvements. Contribute to development and continuous improvement activities related to product design, manufacturing, and control.
Competences:
- Strong knowledge of product lifecycle management, including development, stability, clinical, registration, process transfer, manufacturing, and supply.
- Strong leadership and team management skills, with the ability to guide, delegate, and develop team members. Proven ability to lead cross-functional and cross-regional teams.
- Excellent interpersonal and communication skills, with the ability to present within technical and leadership forums. Strong technical writing capability for reports and scientific documentation.
- Advanced problem-solving, critical thinking, and analytical skills to address complex technical challenges. Demonstrated ability to lead projects to successful outcomes and work across disciplines.
- Self-motivated, resourceful, flexible, and able to manage multiple priorities. Fluent in English.
Education and/or Experience:
- Bachelor’s degree (EQF Level 6) in a scientific discipline (Chemistry, Biology, Pharmaceutics, Chemical Engineering, or related) with 8+ year experience, or Master’s degree (EQF Level 7) with 4+ year experience, or PhD (EQF Level 8) with 1+ year experience.
- Relevant experience in the pharmaceutical or other regulated industry, with a broad background in product development and lifecycle management. Familiarity with analytical techniques and/or process engineering is advantageous.
We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The minimum salary for this position is €36,800.00 annually. Your initial pay could be at the minimum or higher based on skills and expertise, experience, and other relevant factors, all of which are subject to change. This position may also be eligible for competitive benefits, discretionary bonuses, and/or long-term incentive. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.
Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
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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