Vie - Process Development Solution
il y a 3 semaines
**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.
**Summary of your V.I.E mission**:
You will directly support the product development projects of the Solution Process Development Group.
In your role, you will:
- Explore potential new technologies to fulfill manufacturing needs (i.e. lyophilization, spray-drying, powder filling, solution mixing, process analytical technology). Identify and experiment these technologies at lab scale to provide recommendations for transfer to manufacturing plants. Manage the relation and communication with the suppliers.
- Make sound technical recommendations regarding projects/matters (i.e. modification of process parameters for mixing, manufacturing line upgrade, investigations).
- Independently select techniques and procedures to solve problems within area of responsibility. Develop appropriate documentation (i.e. protocol/report, process FMEA ) to support development studies and transfer to Manufacturing plant with strong focus on “solution” aspects of the product.
- Collaborate to the manufacturing development processes by interacting with the design, quality and manufacturing teams.
- Contribute to technical feasibility analysis of complex research and design concepts to deliver robust processes based on Quality by Design and risk-based approach.
- Employ appropriate techniques/methods to successfully and independently execute routine assignments within negotiated deadlines. Identify existing alternative methods and technologies for improving existing or new products/processes.
- Maintain knowledge of relevant regulatory safety requirements (product development, process validation, design and safety) to ensure compliance to the GMP guidelines for human medicines.
- Maintain technical knowledge on manufacturing processes for various product families, technical platforms and plants.
- Communicate continuously to the team and management any progress/status of the studies under your responsibility.
You may be required to travel to other Baxter facilities to support projects execution (up to 25%). Driving license is a must.
**Qualifications**
- Master’s degree in Pharmaceutical Sciences, Biomedical Sciences or Chemical Sciences.
- Fluent in English.
- Knowledge of human medicine regulations is an asset
- Knowledge of MS Office (Excel, Word, Outlook, PowerPoint )
- Knowledge of Lean/Six Sigma tools and statistics is a plus
- Possess relevant laboratory/technical, writing, and computer skills
- Effectively able to contribute on a project team and to work in a matrix organization.
- Take the lead when appropriated to drive a project to completion.
- 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.
- Able to work on relevant lab techniques as well as on commercial scale operations.
- Able to work autonomously.
**Reasonable Accommodations**
**Recruitment Fraud Notice**
Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.
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