V2V Supply Chain Ops Associate - Pharma Compliance

Panda International; Gierle; Sur place; EUR 38 000 - 58 000; Plein temps

Résumé du poste

Panda International in Belgium seeks a Supply Chain Associate to support Vein-to-Vein operations, ensuring compliant, timely handling of patient materials. You will liaise between treatment sites, carriers and internal teams, overseeing logistics, planning and CoC/CoI requirements.

The role requires 1–3 years in a regulated environment, familiarity with GMP/FDA processes, and a proactive approach to continuous improvement within an SAP-enabled supply chain.

Qualifications

• 1–3 years of experience in pharmaceutical or highly regulated environments.
• Familiarity with quality systems, including cGMP and FDA regulations.
• SAP experience is a plus.
• Strong ability to interpret procedures, reports and regulations.
• Attention to detail and scientific judgment.

Responsabilités

• Serve as primary supply chain contact for treatment sites and internal teams within a country/region.
• Support movement of patient materials across the V2V supply chain for EMEA patients.
• Manage issue resolution and non-conformance handling.
• Oversee inbound/outbound logistics and liaise with carrier network.
• Coordinate with warehouses and distribution centers to ensure smooth patient journey.
• Ensure compliance with CoC and CoI across processes.
• Help plan capacity by scheduling cryopreservation and manufacturing slots.
• Support site certification, training delivery, and logistics tests.
• Develop and refine SOPs and WIs with a focus on improvement.
• Contribute to system solutions development, testing, and rollout.
• Track KPIs to monitor efficiency and effectiveness.

Connaissances

pharma industry experience

Quality Systems (cGMP/FDA)

SAP experience

strong communication

regulatory awareness

Outils

SAP

Description du poste

Panda International in Belgium seeks a Supply Chain Associate to support Vein-to-Vein operations, ensuring compliant, timely handling of patient materials. You will liaise between treatment sites, carriers and internal teams, overseeing logistics, planning and CoC/CoI requirements.

The role requires 1–3 years in a regulated environment, familiarity with GMP/FDA processes, and a proactive approach to continuous improvement within an SAP-enabled supply chain.