Manufacturing QMS Consultant Manager – Pharma/Life Sciences, Veeva, Validation

PwC

. Lead client work focused on product development and manufacturing processes, emphasizing quality management systems, validation, and Veeva-enabled solutions .

Posted 10/5/2026full-timeUnited StatesMid-LevelSenior💰 $99,000 - $232,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in leading product development and manufacturing processes within pharmaceutical and life sciences sectors, with a strong focus on quality management systems and Veeva platform applications. Proven ability to manage client engagements, validate processes, and coach teams to enhance operational efficiency.

Highest-signal resume keywords

Veeva QMS ConsultingManufacturing StrategyValidation Activities ManagementQuality Management SystemsClient Engagement Management

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Quality Management SystemsValidation PlanningProcess DocumentationManufacturing StrategyLean PracticesAnalytical ThinkingProject ManagementData AnalysisChange ManagementOperational Improvement

Soft Skills

CoachingProblem SolvingTeam LeadershipClient DeliveryCommunication

Tools & Technologies

Veeva Platform

Industry Keywords

PharmaceuticalLife SciencesRegulated ManufacturingCompliance StandardsOperational Data

About the role

Key responsibilities & impact

Lead client work focused on product development and manufacturing processes, emphasizing quality management systems, validation, and Veeva-enabled solutions
Lead manufacturing quality management system workstreams for pharmaceutical and life sciences clients
Guide teams through validation planning, process documentation, and controlled change activities
Manage client engagements, including deliverables, timelines, budgets, and resource allocation
Review manufacturing strategies, quality processes, and operational data to identify bottlenecks and improvement opportunities
Apply Veeva platform knowledge to support quality workflows, documentation control, and system-enabled process improvement
Translate compliance and standards requirements into operating procedures for regulated manufacturing settings
Coach team members on project execution, problem solving, and client delivery
Monitor deliverable quality, resolve issues, and escalate risks or conflicts

Requirements

What you’ll need

At least a Bachelor's degree
At least 5 years of experience
Preference for study in 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, or Science
Experience demonstrating Veeva QMS consulting in pharmaceutical or life sciences settings
Experience managing validation activities across manufacturing and quality systems
Experience applying manufacturing strategy, lean practices, and process documentation
Experience leading client workstreams, coaching teams, and mentoring junior staff
Analytical thinking to translate system interactions into action
Ability to travel up to 80%
Must not require PwC sponsorship through the H-1B lottery now or in the future, except as set forth in PwC's policy

Benefits

Comp & perks

Annual discretionary bonus
Medical insurance
Dental insurance
Vision insurance
401k
Holiday pay
Vacation
Personal and family sick leave