Senior Director of Process and Platform Development (sterile injectable pharmaceutical scale up from R&D) (On-Site)

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:

Baxter’s Pharmaceuticals Segment delivers differentiated hospital pharmaceuticals in areas of pain, critical care, anti-infection, and oncology. This $2.2B segment includes Injectables & Anesthesia ($1.3B) and Drug Compounding ($.9B) businesses; and reporting 6% annual growth in 2023. Investing in growth opportunities and completing a robust pipeline of product launches are vital for ongoing growth.

As the Senior Director of Process and Platform Development you will join our Pharmaceuticals Research and Development (R&D) team. You will be responsible for leading the development and implementation of sterile manufacturing processes and drug delivery platforms to support the design, development, and scale up manufacturing of Baxter's differentiated pharmaceutical products.  Bring your R&D sterile injectables experience and grow your career making an impact to save and sustain lives!

What You’ll Be Doing:

• Develop and implement strategies for process and platform development, aligning with Baxter's overall business strategy and objectives.

• Collaborate with cross-functional teams to identify process gaps and opportunities for improvement, and develop and implement solutions to enhance efficiency, quality, and speed-to-market.

• Lead the development and implementation of new technologies, tools, and methodologies to support R&D efforts.

• Manage process and platform development priorities, budgets, resources, and timelines, ensuring efficient utilization and adherence to project commitments.

• Foster a culture of continuous improvement, encouraging creativity, and promoting a data-driven mindset within the R&D team.

• Lead and mentor a diverse team of process and platform engineers and scientists, providing guidance, coaching, and support for professional development.

• Build and maintain relationships with external partners, such as suppliers, academic institutions, regulatory bodies, and industry organizations.

• Stay abreast of industry trends, emerging technologies, and competitive landscape, and leverage this knowledge to drive innovation and differentiation in Baxter's R&D efforts.

• Expected travel 10%.

Your Team:

As the Senior Director of Process and Platform Development you will report directly to the Vice President Pharmaceuticals R&D.  Furthermore, you will lead a team of ~20 Process Engineers and work collaboratively across the organization.

Your Location:

The role is located at our R&D facility in the greater Chicago, IL area northern suburb of Round Lake.  Relocation assistance will be considered.  Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a required minimum number of days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. The flexible workplace policy is subject to local laws and legal requirements. At its discretion, Baxter may decide to adjust, suspend, or discontinue as business needs change. 

What You’ll Bring:

• MS or PhD in a relevant engineering or scientific field (e.g., biomedical engineering, materials science, chemistry, or related subject areas).

• Minimum of 10 years of experience in sterile dosage form development and/or drug delivery technologies.

• Knowledge and expertise in process validation.

• Strong understanding of sterile dosage form development and regulatory requirements, including FDA and international standards.

• Demonstrated success in leading and managing cross-functional teams, driving innovation, and delivering high-quality pharmaceutical products.

• Excellent communication, presentation, and interpersonal skills, with the ability to collaborate effectively with internal and external stakeholders.

• Proven ability to lead change, adapt to new challenges, and navigate complex organizational structures.

• Strong analytical, problem-solving, and decision-making skills.

• Experience with digitalization, automation, and data analytics tools and methodologies.

#LI-JR1

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 our employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $208,000 - $286,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses, and/or long-term incentive. 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.

US Benefits at Baxter (except for Puerto Rico)

This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter

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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