Reporting directly to the Senior Director, Supply Chain, the Supply Chain Data and Serialisation Specialist supports technical, regulatory, and compliance activities across the European supply chain network.
This role is responsible for maintaining the data and compliance infrastructure required for pharmaceutical supply chain operations, including Falsified Medicines Directive (FMD) compliance support, serialisation data governance, EMVO (European Medicines Verification Organisation) data submissions, GS1 product coding, and supply chain partner documentation.
The Specialist works closely with manufacturing partners in China, serialization providers, European logistics partners, and internal Quality and Regulatory teams to ensure supply chain data, documentation, and product movements comply with EU GDP, GMP, and FMD requirements.
The role supports new product launches by coordinating master data configuration, supporting serialization setup, verifying packaging data, and tracking supply chain readiness deliverables prior to commercialization.
Operating within a global framework, the Analyst helps ensure the European supply chain remains secure, compliant, and audit-ready by maintaining accurate data, monitoring compliance indicators, supporting investigations, and escalating risks as needed in partnership with Supply Planning, Quality, Commercial, Legal, and Compliance teams.
Benefits:
- Company pension
- On-site parking
- Private medical insurance
- Sick pay
Ability to commute/relocate:
- Cork, County Cork: reliably commute or be willing to relocate with an employer-provided relocation package (required)
Application question(s):
- Do you have experience in developing and operating serialisation and traceability systems?
Experience:
- Pharma supply chain data and serialisation: 5 years (required)
Work authorisation:
Location:
- Cork, County Cork (preferred)
Work Location: Hybrid remote in Cork, County Cork
