Director, Project Management

Envista Holdings Corporation

. Lead the organization’s project management function within a medical device environment .

Posted 10/7/2026full-timeBrea • California • United StatesLead💰 $197,700 - $241,600 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in project management within a regulated medical device environment, focusing on portfolio management, governance, and cross-functional leadership. Proficient in driving execution discipline and continuous improvement while managing KPIs and stakeholder communications.

Highest-signal resume keywords

Project ManagementPortfolio ManagementPeople LeadershipRegulatory ComplianceStakeholder Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project Management MethodologiesRisk ManagementSchedule ManagementGovernance ProcessesAnalytical SkillsProblem-Solving SkillsConflict Resolution

Soft Skills

FacilitationOrganizational SkillsInfluencing SkillsCommunication Skills

Tools & Technologies

Microsoft ProjectExcelPowerPointTeamsSharePointPortfolio Reporting Systems

Certifications & Qualifications

PMPPgMPLean Six SigmaAgile

Industry Keywords

Medical DeviceLife SciencesHealthcare TechnologyISO 13485FDA Quality System RegulationEU MDR

Tech Stack

Tools & technologies

PMP

About the role

Key responsibilities & impact

Lead the organization’s project management function within a medical device environment
Own and manage the Project Priority List, including priorities, sequencing, resources, dependencies, and business impact
Manage program KPIs including on-time delivery, budget, and business impact
Lead, coach, and develop Project Leads, Project Managers, and Program Managers
Conduct monthly portfolio reviews and assess progress, risks, barriers, and priorities
Lead innovation reviews, including portfolio reviews, PPGs, and corporate innovation reviews
Translate innovation strategy into execution KPIs and track progress
Drive governance, standardization, and continuous improvement of project management processes and tools
Partner with senior and functional leaders on trade-offs, resource constraints, portfolio risks, and escalations
Ensure project plans cover scope, schedules, milestones, deliverables, budgets, dependencies, risks, and stakeholder communications
Support medical device development, lifecycle management, quality, regulatory, operations, commercial, and business improvement initiatives
Promote execution discipline in a regulated medical device environment
Develop portfolio metrics, dashboards, and status reporting
Facilitate cross-functional alignment, issue resolution, and timely decision-making
Identify bottlenecks, recommend corrective actions, and improve project predictability, speed, quality, and business value

Requirements

What you’ll need

Must reside within a commutable distance to both Brea, CA and Irvine, CA
Bachelor’s degree in Engineering, Life Sciences, Business, Project Management, or a related field; equivalent combination of education and relevant experience may be considered
Minimum of 10 years of progressive project, program, or portfolio management experience, including experience leading cross-functional initiatives
Minimum of 5 years of people leadership experience
Experience working in the medical device, life sciences, healthcare technology, or other regulated industry
Experience managing project portfolios, priority lists, governance processes, executive reporting, and resource prioritization
Strong knowledge of project management methodologies, portfolio management practices, risk management, schedule management, and stakeholder communication
Ability to influence senior leaders and cross-functional partners without direct authority in complex, matrixed environments
Excellent written and verbal communication skills, including executive-level presentations
Strong analytical, organizational, facilitation, conflict-resolution, and problem-solving skills
Proficiency with Microsoft Project, Excel, PowerPoint, Teams, SharePoint, and portfolio reporting systems
Master’s degree or MBA preferred
PMP, PgMP, Lean Six Sigma, Agile, or similar certification preferred
Experience with medical device product development, design controls, ISO 13485, FDA Quality System Regulation, EU MDR, or related frameworks preferred

Benefits

Comp & perks

Annual performance bonus
Medical benefits
Dental benefits
Vision benefits
401K match
Other applicable compensation plans