Logistics Coordinator

Real; Noord-Brabant; On-site; EUR 60,000 - 80,000; Full time

Job summary

Real is looking for a Logistics Lead in Netherlands to oversee compliance and validation in logistics operations. The role includes ensuring adherence to GMP regulations and fostering a strong quality culture.

Candidates should possess a bachelor's degree with at least 2 years of experience in GMP-regulated environments. Responsibilities involve managing quality systems, compliance audits, and operational excellence initiatives, while collaborating with cross-functional teams.

This is predominantly an on-site position with limited remote flexibility.

Qualifications

• 2+ years experience in a GMP‑regulated manufacturing or logistics environment.
• Strong experience in quality systems, validation, or compliance within pharma/biotech.
• Good understanding of GMP regulations and multi‑authority requirements.

Responsibilities

• Ensure all validation activities are executed in line with regulations.
• Own logistics‑related GMP quality systems.
• Oversee GMP documentation within logistics systems.

Skills

GMP regulations

Quality systems

Project management

Logistics execution systems

Stakeholder management

Continuous improvement

Education

Bachelor's degree or technical education in engineering, logistics, or life sciences

Tools

SAP

MES

Job description

Start: ASAP
End: 6 month contract (initial)
Location: Netherlands - On-site (max. 1 day remote/week)
Hours: Full time (40 hrs/week)
Sector: Life Sciences | Pharmaceutical Industry | GMP Operations & Logistics

About the Role

A leading global pharmaceutical organisation (Novartis) is seeking a Logistics Lead to oversee quality, compliance and validation activities within its logistics operations.

In this role, you will be responsible for ensuring that all logistics processes, systems, and facilities operate in full compliance with GMP and regulatory requirements. You will act as the key interface between logistics, quality assurance, engineering, and external partners, ensuring consistent implementation of global standards at site level.

The position combines quality systems ownership, validation oversight, and operational logistics support, with a strong focus on continuous improvement and inspection readiness. You will work in a highly regulated, international environment with exposure to global stakeholders and strategic initiatives.

This is a hands‑on, site‑based role with high impact on compliance, operational excellence, and business continuity.

Key Responsibilities

• Ensure all validation, revalidation, qualification, and Annual Monitoring Batch (AMB) activities are executed in line with timelines and regulations.
• Own and maintain logistics‑related GMP quality systems in alignment with corporate and regulatory standards.
• Ensure consistent interpretation and implementation of quality manuals (QMs) and global operating procedures (GOPs).
• Monitor quality system performance and generate trend and evaluation reports.
• Oversee GMP documentation and data integrity within logistics systems (e.g. SAP, MES).
• Act as point of contact for compliance topics, audits, and global initiatives.
• Support and oversee third‑party activities, including suppliers and contractors.
• Conduct risk and gap assessments and ensure effective CAPA implementation.
• Maintain inspection readiness across logistics operations.

Operational Excellence & Projects

• Lead and contribute to continuous improvement and productivity initiatives (e.g. 6S).
• Support logistics teams in process optimisation and data‑driven improvements.
• Provide operational support during technology transfers.
• Manage logistics‑related projects, ensuring delivery on time, within scope, and GMP compliance.
• Define technical requirements and contribute to feasibility studies and budgeting.
• Prepare and review technical documentation and specifications.
• Issue URS for new equipment and investments.

Quality & HSE

• Promote a strong quality culture in collaboration with QA.
• Support implementation and continuous improvement of HSE standards.
• Ensure compliance with safety regulations and internal policies.

Profile

• Bachelor's degree or technical education (HF/FH level or equivalent), preferably in engineering, logistics, or life sciences.
• Minimum 2+ years experience in a GMP‑regulated manufacturing or logistics environment.
• Strong experience in quality systems, validation, or compliance within pharma/biotech.
• Good understanding of GMP regulations and multi‑authority requirements.
• Experience with logistics execution systems (e.g. SAP, MES).
• Strong project management and continuous improvement mindset.
• Ability to operate effectively in a cross‑functional, international environment.
• Structured, detail‑oriented, and quality‑driven approach.
• Strong technical and analytical mindset.
• Excellent stakeholder management and communication skills.
• Team player with ability to influence and drive change.
• High level of accuracy and compliance awareness.
• Adaptable, organised, and able to work under pressure.

Additional Information

• Current setup: Day shift (future shift/on‑call requirement).
• Work model: Primarily on‑site.
• Screening: Background check (VGB) and ID verification required.