Senior Director of Process and Platform Development, Baxter

Senior Director of Process and Platform Development

Baxter

Location:

United States, Round Lake

Category:

Research and Development

Contract Type:

Employment contract

Salary:

208000.00 - 286000.00 USD / Year

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Job Description:

As the Senior Director of Process and Platform Development, 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. You will collaborate across teams to innovate, identify process gaps, and implement solutions that enhance efficiency, quality, and speed-to-market. You will lead and mentor a team of engineers and scientists while fostering a culture of continuous improvement and staying abreast of industry trends to drive innovation.

Job Responsibility:

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%

Requirements:

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

What we offer:

Support for Parents
Continuing Education/ Professional Development
Employee Health & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts
Educational assistance programs
Paid holidays
Family and medical leaves of absence
Paid parental leave
Commuting benefits
Employee Discount Program
Employee Assistance Program (EAP)
Childcare benefits

Additional Information:

Job Posted:

March 20, 2025

Employment Type:

Fulltime

Work Type:

On-site work

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