QA-CSV & Digital Checklists Lead — Site (Belgium)

EPM Scientific; Beerse; On-site; EUR 60,000 - 90,000; Full time

Job summary

EPM Scientific is seeking a QA-CSV Specialist & Checklyst Manager Site Key User for a Belgium-based on-site role at a leading pharmaceutical manufacturing site. The position blends CSV quality oversight with governance of a site-wide digital checklist platform.

You will ensure data integrity, manage validation activities, and act as the Site Key User for Checklyst Manager, enabling GMP-compliant digital workflows and robust technical controls across systems.

Qualifications

• QA-CSV support for GMP-regulated computerized systems and data integrity.
• Provide governance and administration for site digital checklists (Checklyst Manager).
• Coordinate validation lifecycle activities and cross-functional risk assessments.

Responsibilities

• Provide QA support across the full computerized system lifecycle: validation planning, IQ/OQ/PQ, change control, improvements.
• Govern digital checklist workflows: create, test, approve, release processes, GMP compliance.

Skills

CSV Validation

Quality Assurance

GxP Compliance

Data Integrity

CAPA Management

Change Control

Risk Management

Validation & Documentation

Regulatory Audits

Inspection Readiness

Education

Bachelor's or Master's in Engineering

Automation

Computer Science

Life Sciences

Biotechnology

Pharmaceutical Sciences

Related discipline

Tools

SIMATIC Logon

Checklyst Manager

Job description

EPM Scientific is seeking a QA-CSV Specialist & Checklyst Manager Site Key User for a Belgium-based on-site role at a leading pharmaceutical manufacturing site. The position blends CSV quality oversight with governance of a site-wide digital checklist platform.

You will ensure data integrity, manage validation activities, and act as the Site Key User for Checklyst Manager, enabling GMP-compliant digital workflows and robust technical controls across systems.