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Senior Director of Process and Platform Development

https://www.baxter.com/ Logo

Baxter

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Location:
United States, Round Lake

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Category:
Research and Development

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Contract Type:
Employment contract

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Salary:

208000.00 - 286000.00 USD / Year

Job Description:

This is where new knowledge is discovered. Baxter’s Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. From Scientists to Engineers, your work creates the products that save and sustain lives. As a Senior Director, you will lead the development and implementation of sterile manufacturing processes and drug delivery platforms to support Baxter's differentiated pharmaceutical products.

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
  • time-off benefits
  • commuting benefits
  • Employee Discount Program
  • Employee Assistance Program (EAP)
  • childcare benefits

Additional Information:

Job Posted:
March 21, 2025

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:
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