Description
Context of the mission:
Baxter International Inc. develops, manufactures, and markets products that save and sustain the lives of people with infectious diseases, trauma, and other chronic medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals, and biotechnology to create products that advance patient care worldwide.
Details of the mission:
- Effectively contribute solid technical knowledge to a variety of projects within the relevant discipline (process development from laboratory to industrial scale) with minimal assistance.
- Display basic technical understanding of related disciplines (formulation, analytical …).
- Conduct routine/non-routine research and design experiments with minimal assistance.
Role and responsibilities:
You will directly support the development of New Product within the Solution Process Development Group, part of the Center of Excellence team of Medical Product and Therapies. In your role, you will:
• Make technical recommendations regarding engineering matters.
• Provide analysis of experimental procedures and adapt as needed.
• Independently select techniques and procedures to solve problems within area of responsibility.
• Develop appropriate documentation (i.e., protocol/report, FMEA…) to support development studies and transfer to Manufacturing plant, including the Process Validation approach.
• Employ appropriate techniques/methods to execute routine assignments successfully and independently within negotiated deadlines. Identify existing alternative methods and technologies for improving existing or new products/processes.
• Maintain knowledge of relevant regulatory & safety requirements to ensure compliance in all research, data collection and reporting activities.
• Maintain technical knowledge on manufacturing processes for various product families, technical platforms, and plants. Contribute to technical scale-up activities and transfers to plants.
• Have a working knowledge and understanding of GMP and related regulations and guidance.