Continuous Improvement Project Manager

Tulip Interfaces

. Own project plans, timelines, budgets, and deliverables with cross-functional teams and customers, from scoping and quoting through go-live .

Posted 11/12/2026full-timeRemote • GermanyMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in project management for regulated life sciences, focusing on delivering successful outcomes through effective communication, collaboration, and compliance with quality systems. Proficient in managing project plans and timelines while guiding customers through digital transformation initiatives.

Highest-signal resume keywords

Project ManagementRegulated Quality SystemsClear CommunicationFluent French and EnglishLean / Six Sigma

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project PlanningRisk ManagementDigital TransformationCompliance FrameworksManufacturing Operations

Soft Skills

CollaborationOrganizational SkillsLeadershipDecision-Making

Certifications & Qualifications

PMP CertificationAgile Certification

Industry Keywords

GxPISO Standards21 CFR Part 11PharmaBiotechMedical Device

Tech Stack

Tools & technologies

PMP

About the role

Key responsibilities & impact

Own project plans, timelines, budgets, and deliverables with cross-functional teams and customers, from scoping and quoting through go-live
Partner with customers and internal experts to define requirements and what success looks like
Work on-site with customers (about 25% travel) and guide them through their manufacturing digital transformation
Keep information and communication organized so teams can stay focused on the work
Understand the technical details well enough to manage risk and escalate when needed
Help improve how Professional Services delivers, including building out new AI-assisted workflows
Collaborate with customers, Tulip's partners, internal customer-facing technical teams, and sales and commercial leadership

Requirements

What you’ll need

5+ years of experience delivering projects for regulated life sciences customers (pharma, biotech, or medical device), in project or program management, manufacturing operations, consulting, or customer success
Strong working knowledge of regulated quality systems and compliance frameworks, including GxP, ISO standards, and 21 CFR Part 11
Experience building and running detailed project plans (scope, milestones, owners, timelines) across internal teams, partners, and customers at multi-site, multi-region organizations
Clear written and verbal communication, including leading project meetings, driving decisions, and giving executive-level updates to technical and non-technical audiences
Fluent French and English required
Nice to have: Lean / Six Sigma, Agile, or PMP certification, plus familiarity with change control and validation in regulated environments

Benefits

Comp & perks

Direct impact on product and culture
Company equity
Competitive benefits package including Health, Dental, Vision, Short-term Disability, Long-term Disability, Life Insurance, AD&D Insurance, Flexible Spending Account (FSA), Commuter Benefits, Parental Leave, and 401(K)
Flexible work schedule and unlimited vacation policy
Learning & Development program
Virtual company events and happy hours
Fitness subsidies