Principal Engineer, Sterility Assurance (Relocation Assistance Available)

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. 

Your role at Baxter

The research we do and the products we develop improve outcomes for patients around the world. At Baxter, your work contributes directly to making a significant impact on others. It's ambitious work—and you're not on your own. Our teams collaborate cross-functionally and lead by influence. Whether guiding a team through a project or leading direct reports, our research and development team is responsible for influencing others to achieve results. Our colleagues within our R&D organization desire to work on products that make an important difference in others' lives. We are motivated by the power of collaboration and are natural leaders who are skilled at influencing others.

Your team

As a Principal Engineer at Baxter, you will provide Sterility Assurance leadership and technical support to multi-disciplinary product development teams, domestic/international manufacturing facilities, Regulatory Affairs and internal Sterility Assurance customers.  You will act as the Sterility Assurance Project Lead (Focal Point) for new product development, sustaining product support, and manufacturing facility VIP initiatives.

What you'll be doing:

• Coordinate, prioritize, and manage multiple Sterility Assurance-related activities with minimal guidance

• ​Provide input for schedules, budget, product requirements, and design

• Provide support for regulatory submissions

• Liaise with cross-functional project teams and manufacturing facilities to develop validation plan (i.e. Rationale Statement) and sterilization parameters for product development

• Lead and support product development studies

• Lead agile Sterility Assurance internal project meetings

• Effectively communicate program status to multi-disciplinary project team members, management, key stakeholders

• Provide support for complex investigations, troubleshooting, and CAPAs.  

• Evaluate data/results relative to product requirements, definitions and/or program goals.

What you'll bring:

• B.S. in Engineering field and 5 + years of related experience.

• General knowledge of sterilization modalities and regulatory requirements for sterile medical products (Moist Heat, Ethylene Oxide, Radiation [gamma, electron beam, X-ray], Aseptic Processing).

• Ability to drive complex decision-making and influence courses of action using both written and verbal methods.

• Ability to design experiments and draw meaningful conclusions from data using statistical methods such as descriptive, diagnostic, predictive and prescriptive analytics desirable.

• Effectively operate in and may facilitate cross-functional teams with minimal guidance.

• Ability to provide solutions that reflect understanding of business objectives and cost implications.

Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $104,000 to $143,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview. #LI-ASR2

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

EEO is the Law 
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Pay Transparency Policy

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

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