Senior Consultant: AI-Driven Product Delivery

Experis; Batesville (IN); On-site; USD 117,000 - 143,000; Full time

Benefits offered by this job

Medical and Prescription Drug Plans

Vision Plan

Health Savings Account

Health Flexible Spending Account

Dependent Care Flexible Spending
Accnt

Supplemental Life Insurance

Short Term and Long Term Disability
In

Business Travel Insurance

Weekly Pay

Job summary

Experis seeks a Senior Consultant to lead a 12-month initiative to simplify end-to-end product development processes across R&D, Quality, Regulatory, and other functions. You will map current PDE and QMS flows and drive AI-enabled improvements that increase speed, quality, and compliance.

The role requires a strong background in engineering or science, with 15+ years in medical products, plus expertise in FDA QSR and ISO 13485.

Qualifications

• Bachelor's degree in engineering, science, quality, operations, or a related field; advanced degree preferred.
• Typically 15+ years in product development, quality systems, operational excellence, process engineering, program management, or related disciplines in medical products.
• Working knowledge of FDA Quality System requirements and ISO 13485; demonstrated success in cross-functional transformation.

Responsibilities

• Lead a 12-month engagement to simplify end-to-end product development processes.
• Map PDE and QMS flows, quantify friction points, and align stakeholders on a prioritized roadmap.
• Redesign and pilot high-priority processes with governed AI use cases to improve speed, quality, and compliance.
• Clarify ownership, decision rights, roles, interfaces, and phase criteria across shared processes.
• Drive measurable results through performance tracking and transition ownership with a sustaining plan.

Skills

Leadership

Stakeholder management

Facilitation

Change leadership

Process improvement

Education

Bachelor's degree

Advanced degree preferred

Job description

Experis seeks a Senior Consultant to lead a 12-month initiative to simplify end-to-end product development processes across R&D, Quality, Regulatory, and other functions. You will map current PDE and QMS flows and drive AI-enabled improvements that increase speed, quality, and compliance.

The role requires a strong background in engineering or science, with 15+ years in medical products, plus expertise in FDA QSR and ISO 13485.