**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.
**About Us: Baxter´s mission**:
Our products and therapies touch the lives of millions of people around the world every day, which is why we are passionate about ground-breaking innovations that bring more personalized care to all of us. For 87 years and counting, we have been at the critical intersection where the ideas that save and sustain lives meet the providers who make it all happen. And now, we are determined to realize our boldest opportunities to transform global healthcare for years to come.
**Your team**
There hasn't been a better time to join Baxter!
We develop quality products with the patient in mind, so our marketing efforts are also patient-centric. That means you can be proud of our work and the value we provide to people every day.
As a large, multinational organization, you have the opportunity to expand your knowledge through collaboration with a variety of individuals, exposure to different facets of our portfolio, and an encouraging leadership team that allows ongoing development.
**Your role at Baxter**
This position is accountable for leading and performing activities in support of the validation and compliance of a computerized system to ensure system meets its's intended use.
**What you'll be doing**
- Responsible for the conduct of Verification and Validation activities as per requirements defined in Baxter Design Control Method and regulatory requirements
- Responsible for assuring the new Computerized System meets the requirements of the systems users and coordinate risk management actions
- Crafting, managing, and /or maintaining the documents required by Baxter quality systems procedures
- Responsible for oversight of protocol execution
- Communicate and control the alignment to validation standards by the team
- Provide support to the functional team/users for the development of validation results (functional specification, technical specification, system & user procedures, etc)
**What you'll bring**
- 5 years of shown experience in validation industry standards;
- Detailed knowledge of GxP regulations (e.g. 21 CFR Part 11, GAMP 5, MHRA etc.), Standards, and Industry Best Practices.
- Knowledge of data privacy regulation;
- Good communication
- Basis project management skills
- Understanding of software development/implementation processes.
- Excellent technical writing skills
- Self-motivated, detail oriented, takes initiative and ability to work independently without close supervision.
- Knowledge and experience in the following areas:
- Documentation Management using document management tool
- Test Management tool HP Quality Center
- Agile Scrum Principle
- Proficient in English
- MSOffice, TcU, ServiceNow, HP ALM.
- Travels may be required (1 or 2 per year)
This is where you make a real impact!
**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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