Manufacturing QMS Consultant Manager (Pharma/Life Sciences, Veeva, Validation)

PwC•St. Louis, MO

1d•$99,000 - $232,000•Remote

About The Position

As a Manufacturing QMS Consultant Manager, you will lead client work focused on product development and manufacturing processes, with an emphasis on quality management systems, validation, and Veeva-enabled solutions within our Operations Consulting practice. As a Manager, you will coach teams, manage project workstreams, and apply sound judgment to review deliverables, guide problem-solving, and support client priorities across complex engagements. In this role at PwC, you will help clients streamline processes, improve productivity, reduce waste, and strengthen quality across the product lifecycle while working across cross-functional teams and using digital tools to support delivery.

Requirements

At least a Bachelor's degree
At least 5 years of experience

Nice To Haves

Preference for at least one of the following fields of study: Analytics/Data Science, Artificial Intelligence/Robotics, Biology/Biomedical Sciences, Business Administration/Management, Computer Science/Information Systems, Engineering, Environmental Science/Sustainability, Health Administration/Public Health, Mathematics/Statistics, Operations/Supply Chain, Project/Technology Management, Science
Demonstrating Veeva QMS consulting in pharmaceutical or life sciences settings
Managing validation activities across manufacturing and quality systems
Applying manufacturing strategy, lean practices, and process documentation
Leading client workstreams, coaching teams, and mentoring junior staff
Using analytical thinking to translate system interactions into action

Responsibilities

Leading manufacturing quality management system workstreams for pharmaceutical and life sciences clients
Guiding teams through validation planning, process documentation, and controlled change activities across product development and manufacturing environments
Managing client engagements by prioritizing deliverables, timelines, budgets, and resource allocation
Reviewing manufacturing strategies, quality processes, and operational data to identify bottlenecks and improvement opportunities
Applying Veeva platform knowledge to support quality workflows, documentation control, and system-enabled process improvement
Translating compliance and standards requirements into practical operating procedures for regulated manufacturing settings
Coaching team members on project execution, problem solving, and client delivery across multiple workstreams
Monitoring deliverable quality, resolving issues, and escalating risks or conflicts when needed