Senior Engineer R&d

hace 6 meses

Monterrey, México BAXTER A tiempo completo

**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 focused on transformative innovations that bring smarter, 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 role at Baxter**:
As part of an R&D project team, the Senior Engineer Systems/V&V provides technical contributions to the system design and Verification/Validation of a complex medical device from concept through commercialization and/or through the full life cycle of the product. A senior engineer focuses on create or sustaining the customer needs; creating or modifying product system requirements and architecture necessary to meet those needs; evaluates constraints and makes trade off decisions; contributes to the development or modifications to system/module level design requirements; contributes to the product safety and security risk management activities including DFMEA’s, RA´s; contributes to the identification of technical risks and mitigations, develops the verification and validation plans, protocols, scripts, execution, regression, and reports, for small to medium projects and/or designated segments of larger complex projects. May provide guidance to other engineers on their technical issues, engage in design reviews and help resolve problems of medium complexity.

**Your team**:
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 a supportive leadership team that encourages ongoing development

**What you'll be doing**
- Fulfill the duties adhering to the culture of compliance with standards and ethical business practices in the organization.
- Follow and drive compliance with Baxter policies and the Code of Conduct.
- Implement Baxter's code of conduct, policies and procedures, including, but not limited to, the Global Interactions Policy and Third Party Policy.
- Applies technical competencies and knowledge to solve problems of a routine nature or improve upon existing designs or processes.
- Implementation of Change Requests (CR/CO’s) in the Agile PLM system (detail design drawings, schematics, specifications, and bills of material).
- Responsible for the accurate documentation of designs through the generation and maintenance of design requirement specifications, product drawings, component drawings, material specifications and bills of materials.
- Ability to utilize critical thinking to solve issues.
- Seeks input from more experienced individuals to improve quality of deliverables.
- Frequent collaboration and coordination with other functions, other Hill-Rom manufacturing sites, critical suppliers, and design partners may be required depending on projects assignments.
- Applies new technical tools and concepts under the direction of others.
- Other duties may be assigned.

**What you'll bring**
- Bachelor’s Degree in Engineering (mechanical, bio-mechanical, MET) or local equivalent of same.
- 2-7 years of experience (no minimum).
- Ability to generate alternative solutions to problems or processes.
- Strong Interpersonal skills with the ability to work collaboratively with others in a team environment.
- Ability to adapt to Change.
- Good judgment in selection methods and techniques to acquire results.
- Knowledge of Medical Device Regulations and Standards including design control and risk management is preferred.
- Proficient in systems engineering tools such as DOORS, Weibull, Minitab, statistical tools. Green Belt, Black Belt, Six Sigma tools, FDA 21 CFR 820, ISO9001, ISO13485 and UL Medical std are preferred.
- Strong technical writing and communication skills.
- Self-motivated with high performance stand

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