PROCESS DEVELOPMENT ENGINEER (SOLUTION) GB

Job description

BELGIQUE(Braine-L'Alleud)
du01 janvier 2020au01 janvier 2021(pour12mois)
ETABLISSEMENT :BAXTER SAS
REMUNERATION MENSUELLE :1809€ (indemnité non contractuelle fixée par décret et arrêté, dont le montant peut varier notamment en
fonction de l’évolution du barème de référence, de la localisation de la mission et des cas d’abattements prévus par les textes)

BAXTER:

Baxter International Inc. develops, manufactures and markets products that save and sustain the lives of people with infectious diseases, kidney disease, trauma, and other chronic and acute 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.

ESSENTIAL DUTIES AND RESPONSABILITIES:

• Effectively contribute to build solid technical knowledge to a variety of projects within multi-disciplinary environment with autonomy.
• Display technical understanding of disciplines related to formulation, emulsion, chemical engineering, and process validation in pharmaceutical environment.
• Conduct routine/non-routine research and design experiments at laboratory, Pilot and manufacturing scale.
• Effectively apply data analysis methodology to support critical decision making

1. Make sound technical recommendations regarding projects/matters that are out of routine. Develop appropriate documentation to support development studies from exploratory research to Process Validation.
2. Employ appropriate techniques/methods to successfully and independently execute routine and non-routine assignments within timelines. Identify existing alternative methods and technologies for improving existing or new products/processes.
3. Maintain knowledge of relevant regulatory safety requirements while building knowledge of other regulatory requirements related to R&D (product development, process validation, design and safety) to ensure compliance in all research, data collection and reporting activities.
4. Have a working knowledge and understanding of GMP and related regulations and guidance for human medicines. Provide constructive feedback of key experimental procedures for improvement.
5. Contribute to technical feasibility analysis of complex research and design concepts. Recommend appropriate designs, techniques, processes and statistical analysis for specific sequence of tasks where needed.
6. Maintain technical knowledge on manufacturing processes for various product families, technical platforms and plants. Contribute to technical scale-up activities and transfers to plants. Accurately assess results for validity and conformance to specifications.

PROFILE:

Master’s degree in Chemical Engineering, Physico-chemical Sciences or Pharmaceutical Sciences
1-2 years experience or Bachelor’s degree with 2-4 years of related experience.
Fluent in English
Knowledge of MS Office (Excel, Word, Outlook, PowerPoint…)
Knowledge of Lean/Six Sigma tools and statistics is a plus
Driving license and a car are requested

•Possess relevant laboratory/technical, writing, and computer skills.
•Effectively able to contribute on a project team and to work in a matrix organization.
•Demonstrates flexibility and can shift gears comfortably.
•Ability to objectively assess, organize, and clearly communicate complex information.
•Interpret available information and make recommendations to resolve technical challenges.
•Appropriately prioritize assignments to meet project schedules and prioritize multiple tasks in a fast paced environment.
•Effectively able to work on relevant lab techniques as well as commercial scale operations.