Global Compliance Lead

CIPEx - Consejo de Ingenieros Peruanos en el EXterior; A distancia; EUR 80.000 - 120.000; Jornada completa

Descripción de la vacante

A leading international organization is seeking a Global Compliance Lead to shape the future of digital quality globally. The ideal candidate will harmonize critical quality topics, oversee data integrity, and lead validation strategies across multiple systems. Applicants should have over 10 years of experience in validation management, a strong grasp of GMP and digital compliance, and excellent leadership skills. This role offers an exciting opportunity for digital transformation at a global scale.

Formación

• 10+ years of validation management experience in manufacturing, supply chain, and laboratory environments.
• Proven expertise with MES, LIMS, WMS, ERP validation.
• Experience leading international, multidisciplinary teams in matrix environments.
• Fluent in English.

Responsabilidades

• Be the Compliance Champion managing quality topics.
• Oversee end-to-end data flows ensuring robust controls.
• Define and execute global validation master plans.
• Manage IQ/OQ/PQ protocols, traceability matrices.
• Act as the bridge between sites, QA, and global teams.
• Provide expert guidance on GxP compliance and CSV standards.
• Define resource needs and manage risks proactively.

Conocimientos

Validation management

GMP knowledge

Stakeholder management

Leadership

Effective communication

Digital compliance expertise

Educación

Bachelor’s or Master’s in Engineering, IT, Life Sciences, or related field

Herramientas

MES

LIMS

WMS

ERP

Descripción del empleo

Global Compliance Lead - Contract - 12+ Months - Remote - Pharma - Jan Start

What You’ll Do

• Be the Compliance Champion: Harmonize critical quality topics — from lot number logic and expiry dates to quarantine rules and traceability.
• Own Data Integrity: Oversee end-to-end data flows, ensuring robust controls and global SOPs are in place.
• Lead Validation Strategy: Define and execute global validation master plans for MES, WMS, ERP, and laboratory systems.
• Drive Execution: Manage IQ/OQ/PQ protocols, traceability matrices, and validation documentation with precision.
• Engage Stakeholders: Act as the bridge between sites, QA, and global validation teams, securing buy-in and smooth execution.
• Train & Inspire: Provide expert guidance on GxP compliance and CSV standards, supporting adoption of digital tools.
• Deliver Results: Define resource needs, manage risks proactively, and ensure milestones are hit on time.

What You Bring

• Bachelor’s or Master’s in Engineering, IT, Life Sciences, or related field.
• 10+ years of validation management experience in manufacturing, supply chain, and laboratory environments.
• Proven expertise with MES, LIMS, SDC, WMS, ERP validation.
• Strong knowledge of GMP, GDP, and digital compliance frameworks.
• Experience leading international, multidisciplinary teams in matrix environments.
• Excellent communication, stakeholder management, and leadership skills.
• Fluent in English.

Why This Role Matters

This isn’t just another compliance role — it’s about shaping the future of digital quality across global operations. You’ll be at the forefront of innovation, ensuring that cutting‑edge solutions meet the highest standards of compliance and validation, while empowering teams worldwide to embrace digital transformation.

Ready to Lead?

Ready to lead? If you’re passionate about compliance, thrive in global environments, and want to leave your mark on digital transformation, we want to hear from you.

Apply now or email me at ****** and take the lead in driving compliance and validation excellence on a global scale!