Program Manager with Medical Products Industry

Evolutyz Corp; Chesterfield (MO); Hybrid; USD 180,000 - 250,000; Full time

Benefits offered by this job

Dynamic environment

Cross-functional collaboration

Impact on patient safety and quality

Job summary

Evolutyz Corp is seeking a senior leader in medical device process improvement to map PDE and QMS workflows, drive cross-functional transformation, and implement AI-enabled automation. Hybrid workplace in the United States with extensive senior stakeholder interaction and a focus on patient safety and regulatory compliance.

The role emphasizes Lean Six Sigma, cross-functional leadership, and measurable cycle-time reductions, with a multi-year roadmap and substantial autonomy to deliver

Qualifications

• Bachelor's degree in a related field is required.
• Advanced degree is preferred.
• Typically, 15+ years of experience in product development, quality systems, operational excellence, or related discipline.

Responsibilities

• Assess and map end-to-end PDE, QMS, and related processes affecting R&D.
• Collaborate to establish current-state cycle time, effort, handoffs, rework, and pain points.
• Develop and maintain a prioritized process simplification roadmap based on business value and risk.
• Redesign high-priority processes to eliminate unnecessary steps while preserving patient safety and regulatory compliance.
• Partner with Quality and Regulatory leaders to align PDE practices and local procedures.
• Identify and implement AI and automation use cases for drafting, review, search, data prep, traceability.
• Lead pilots, measure outcomes, and refine solutions prior to broader deployment.
• Develop updated procedures, job aids, and training materials.
• Enable process owners to sustain improvements after engagement.
• Provide recommendations and updates to R&D PMO leadership and stakeholders.
• Lead change across functions and resolve competing priorities.
• First 90 days: map priority PDE and QMS flows; align stakeholders.
• Months 4–9: redesign and pilot end-to-end processes with AI governance.
• Months 10–12: demonstrate measurable reductions and transition ownership.

Skills

Regulatory Knowledge

Quality Systems

Process Improvement

Cross-functional leadership

Automation / AI in workflows

Stakeholder management

Executive communication

Independence & accountability

Education

Bachelor's degree in engineering, science, quality, operations, or related field

Advanced degree preferred

Job description

Summary

Location: Batesville, IN, USA

Duration: 12 Months

Work Arrangement: Hybrid

Key Areas: Medical device, Process Improvement, Six Sigma

Responsibilities

• Assess and map end-to-end PDE, QMS, and related business processes affecting R&D.
• Collaborate with teams to establish current-state cycle time, effort, handoffs, rework, and pain points.
• Develop and maintain a prioritized process simplification roadmap based on business value, compliance risk, effort removed, cycle-time reduction, and stakeholder readiness.
• Redesign high-priority processes to eliminate unnecessary steps, redundant activities, duplicate documentation, and unclear handoffs while preserving patient safety, product quality, and regulatory compliance.
• Partner with Quality and Regulatory leaders to align PDE practices, quality system requirements, local procedures, and working-level execution before piloting or deploying changes.
• Identify, prioritize, and implement practical AI and automation use cases for document drafting, review, search, data preparation, traceability, and knowledge retrieval.
• Lead pilots, measure before-and-after performance, capture lessons learned, and refine solutions prior to broader deployment.
• Develop updated procedures, job aids, reusable patterns, and training materials.
• Enable process owners and teams to sustain improvements after the engagement.
• Provide clear recommendations, progress updates, risks, and decisions to R&D; PMO leadership and cross-functional stakeholders.
• Lead change through influence, facilitate alignment across functions, and resolve competing priorities without direct authority.
• First 90 days: Complete a current-state map of priority PDE and QMS flows, quantify the most significant friction points, and align stakeholders on a prioritized simplification and AI opportunity roadmap.
• Months 4–9: Redesign and pilot two to three processes end to end, deploy selected AI use cases with governance in place, and release updated procedures, tools, and training.
• Months 10–12: Demonstrate measurable reductions in development cycle time, process effort, or rework, document adoption and control effectiveness, and transition ownership with a sustaining plan.
• Core measures: Cycle time, effort removed, rework reduction, adoption, process compliance, user feedback, and sustainability of results.

Requirements

• Bachelor's degree in engineering, science, quality, operations, business, or a related field — required.
• Advanced degree preferred.
• Typically, 15 or more years of experience in product development, quality systems, operational excellence, process engineering, program management, or a related discipline.
• Significant experience in the medical products industry.
• Experience with validated systems, regulated digital tools, data governance, or AI governance.

Required Skills

• Regulatory & Quality Knowledge: Deep knowledge of medical device or other regulated product development, design controls, change control, design history documentation, quality system requirements, working knowledge of FDA Quality System requirements and ISO 13485.
• Process Improvement: Demonstrated success leading end-to-end process improvement across multiple functions, sites, or business units, expertise in Lean, Six Sigma, value-stream mapping, or equivalent process optimization methods, record of delivering measurable results.
• Experience leading complex, cross-functional transformation or continuous-improvement initiatives in a matrixed organization.
• Practical experience applying automation and AI to business or technical workflows, preferably in a regulated environment.
• Ability to translate complex regulatory and process requirements into clear, efficient, and usable ways of working.
• Strong facilitation, change leadership, and stakeholder-management skills.
• Ability to influence senior leaders and subject-matter experts.
• Demonstrated ability to establish metrics, analyze process performance, prioritize opportunities, and communicate recommendations to leadership.
• Excellent written and verbal communication skills.
• Credible with engineers, quality professionals, regulatory partners, and auditors.
• High degree of independence and accountability for results in an ambiguous, cross-functional environment.
• Commitment to Baxter's mission, patient safety, quality, and leadership expectations.

Preferred Skills

• Lean Six Sigma certification or equivalent demonstrated mastery.

Benefits

• Opportunity to work in a dynamic and innovative environment.
• Engage with cross-functional partners in Operations, Manufacturing, Supply Chain, Marketing, Medical, Service, Information Technology, Data Privacy, and other functions affecting product development.
• Contribute to initiatives that enhance patient safety, product quality, and regulatory compliance.