This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
This is where new knowledge is discovered. Baxter’s Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. From Scientists to Engineers, your work creates the products that save and sustain lives. This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.
Job Responsibility
Effectively contributing solid technical knowledge to a variety Stability projects (NPD or SPO) with minimal assistance
Ensuring stability study initiation, study protocol and reports writing, results review and evaluation
Displaying basic technical understanding of theories & practices related to solutions stability
Participate in the development of stability programs: establish routine stability strategies in agreement with the technical leader, analytical leader and regulatory affairs
Accurately assess results for validity and conformance to specifications
Support lab sample preparations by participating in lab related investigations that correspond to atypical or out-of-specifications / out-of-trend test results
Without assistance, make sound technical recommendations regarding project thar are more routine than not
Maintain knowledge of relevant Quality System requirements and safety requirements while building knowledge of other regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities
Employ appropriate techniques/methods to successfully and independently execute routine assignments within negotiated deadlines
Have a working knowledge and understanding of GxP and related regulations and guidance
Demonstrate ability to anticipate risks, issues and opportunities, work independently to make sound technical recommendations regarding projects, and collaborate with team to devise mitigations and solutions
Contribute to technical feasibility analysis of complex research and design concepts
Coordinate and manage interactions with Contract Research Organizations (CROs) to ensure timely, high-quality delivery of outsourced activities aligned with project objectives
Requirements
Fluent in English (read, write, speak)
Possess relevant laboratory/technical/analytical, writing, and computer skills
Effectively able to contribute on a project team
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
Master’s in science: for instance, Analytical, Organic chemistry, Biochemistry, Bio-engineering, Pharma Science
6-10 years of experience in pharmaceutical industry, R&D, manufacturing…
Demonstrate Quality and compliance-oriented accomplishments
Possess basic understanding of analytical chemistry including theoretical knowledge and practical experience
Knowledge of GLP and GMP is a must
Fluent spoken, read, and written English is a must