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Baxter International

Global provider of medical care products

Director – Product Stewardship & Regulatory Programs

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeDeerfield, IL, USA

About the Job

Requirements

  • A bachelor's degree in Engineering, Chemistry, Environmental Science, Regulatory Affairs, Life Sciences, Business, or a related field is required.
  • At least 10 years of experience in product stewardship, regulatory affairs, environmental compliance, product compliance, quality systems, or related disciplines is required.
  • Demonstrated experience leading complex global compliance or regulatory implementation programs is required.
  • A strong understanding of environmental and social regulations affecting products, packaging, chemicals, materials, and supply chains is required.
  • Exceptional project management and execution skills are required.
  • Proven ability to lead large cross-functional initiatives and drive organizational accountability is required.
  • Strong business acumen and the ability to translate regulatory developments into practical business actions are required.

Responsibilities

  • Lead Baxter's global monitoring and assessment of environmental, product, packaging, chemical, circular economy, and social regulatory developments.
  • Establish structured processes to evaluate regulatory applicability across business segments, product categories, and geographic markets.
  • Develop risk assessments and implementation plans for emerging regulations.
  • Maintain an enterprise regulatory roadmap and prioritization framework.
  • Provide actionable recommendations to segment leaders regarding potential business impacts and required actions.
  • Lead execution of product stewardship programs addressing chemicals compliance, packaging regulations, extended producer responsibility requirements, product environmental requirements, human rights due diligence, and other emerging obligations.
  • Establish governance, timelines, milestones, and accountability mechanisms to ensure on-time implementation.
  • Drive enterprise-wide readiness activities and compliance programs.
  • Track progress, escalate risks, and ensure effective issue resolution.
  • Develop and oversee internal reporting mechanisms for compliance status, milestones, and program performance.
  • Partner with business segments to identify areas where Baxter can proactively address future regulatory requirements.
  • Translate regulatory trends into opportunities for product and portfolio innovation.
  • Support development of sustainable product, packaging, and material solutions that position Baxter ahead of future requirements.
  • Enable first-to-market approaches where emerging regulatory trends create opportunities for competitive differentiation.
  • Ensure product stewardship considerations are incorporated into new product development and lifecycle management processes.
  • Lead large-scale cross-functional initiatives involving R&D, Quality, Regulatory Affairs, Legal, Procurement, Supply Chain, Operations, and Commercial teams.
  • Establish clear ownership, decision-making structures, and implementation plans.
  • Drive execution through disciplined project management practices.
  • Remove barriers, resolve conflicts, and maintain momentum across multiple concurrent programs.
  • Build repeatable processes and operating mechanisms to scale regulatory compliance efforts across Baxter.
  • Partner with Commercial Sustainability and segment leadership teams to understand evolving customer requirements and market expectations.
  • Provide regulatory and product sustainability expertise to support customer tenders, audits, questionnaires, and product inquiries.
  • Help commercial teams understand how regulatory trends may influence future purchasing decisions and customer expectations.
  • Support development of product-level sustainability information and compliance documentation needed for customers and health systems.
  • Lead the Product Stewardship function and associated governance forums.
  • Provide regular updates to the Sustainability Leadership Team and executive leadership.
  • Build strong partnerships across business segments and functional organizations.
  • Foster a culture of accountability, execution excellence, and proactive problem solving.

Desired Qualifications

  • Medical device, pharmaceutical, healthcare, or other highly regulated industry experience is preferred.
  • Experience with REACH, RoHS, PFAS regulations, Packaging and Packaging Waste Regulation (PPWR), Extended Producer Responsibility (EPR), conflict minerals, and human rights due diligence requirements is preferred.
  • Experience working directly with product development, R&D, quality, and regulatory teams is preferred.
  • Program Management Professional (PMP) certification or equivalent project management experience is preferred.
  • Experience supporting customer sustainability requests, tenders, or product-level regulatory disclosures is preferred.

About the Company

Baxter International

Global provider of medical care products

Baxter International develops and manufactures medical products and equipment for hospitals and blood banks. Its products include sterile IV solutions and blood storage containers; innovations like the Transfuso-Vac extended blood shelf life, and a plastic blood bag helped shape modern blood banking. The company differs from competitors through a long track record of sterile manufacturing, blood-storage innovations, and strategic mergers that broaden its product portfolio. Its goal is to provide reliable, safe medical products that support patient care and hospital operations worldwide.

Company size
10,001+
Company stage
IPO
Headquarters
Deerfield, IL
Founded
1931

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