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 global pharmaceutical firm is seeking a Global Compliance Lead to drive compliance and validation excellence across digital solutions. This role requires a strong background in validation management, with proven experience in MES, LIMS, WMS, and ERP systems. The ideal candidate will define global compliance strategies, oversee vast data integrity efforts, and engage multidisciplinary teams. Fluency in English and a relevant degree are essential for success in this pivotal position. Join us in shaping the future of digital quality in the pharma industry.

Formación

• 10+ years of validation management experience in manufacturing and laboratory environments.
• Proven expertise with MES, LIMS, WMS, ERP validation.
• Strong knowledge of GMP, GDP, and digital compliance frameworks.

Responsabilidades

• Define global strategies and ensure regulatory integrity in operations.
• Oversee end-to-end data flows and ensure robust controls are in place.
• Manage IQ/OQ/PQ protocols and validation documentation.

Conocimientos

Validation Management

GMP Knowledge

Stakeholder Management

Leadership

Data Integrity

Educación

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

Herramientas

MES

LIMS

WMS

ERP

Descripción del empleo

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

Are you ready to take the lead in driving compliance and validation excellence across cutting‑edge digital solutions?

This is your chance to step into a pivotal role where you’ll define global strategies, ensure regulatory integrity, and champion digital transformation across manufacturing, supply chain, and laboratory environments.

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?

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!