Supply Chain Associate | English C1

What will you do?

• Ensures that all returned Finished Drug Products (FDP) are processed within the agreed timelines and in accordance with applicable regulations and guidelines.
• Coordinates reverse flow process with various internal and external stakeholders. From the transport booking notification until the physical receipt of the returned goods at the warehouses.
• Supports business and system improvements.
• Acts as the primary point of contact for issues related to carrier transport returns and issue resolution.

Responsibilities

• Monitors and coordinates the return of Finished Drug Products (FDP) to all warehouse locations. Including re-calls.
• Maintains and manages metrics and dashboards related to returns under the GSHE scope.
• Ensures all relevant Supply Chain activities comply with applicable regulations, including GDP, GMP, and SOX.
• Participates in internal and external audits as needed.
• Presents the return metrics and dashboard during monthly meetings with various stakeholders or whenever necessary.
• Coordinates with related stakeholders daily to ensure timely completion of required actions from the reverse logistics tracking tool's exception list.
• Identifies potential issues and drives continuous improvement to increase effectiveness and efficiency within processes.
• Updates and maintenance of GxP-controlled documents.

Requirements:

Minimum Requirements

• Master’s degree or Bachelor’s degree & 2 years of Supply Chain experience in a GMP and/or GDP regulated industry
• Ability to multitask and work with a diverse, international group.
• Computer skills and ERP experience
• Experience with issue handling in a logistic environment
• Proactive self-starter who can manage workload and prioritise tasks efficiently.
• Proficiency in the English language is required for both written and oral communication.

Preferred Requirements

• Preferably 3+ yrs' relevant experience in the biotech/pharma industry & strong understanding of supply chain, order-to-invoicing & international trade.
• Advanced understanding of GMP regulations, GDP guidelines, and SOX regulations.
• Lean Six Sigma certification.

Salary Benefits:

• A challenging work environment with excellent career development programs.
• You have the opportunity to grow within the company and to fully develop your skills and competences.
• Hybrid position, twice per week on site in Breda. in the first 2 months you have to be more olften in the office due to training.
• Reimbursement of travel expenses is dependable on travel distance.
• It is important that you reside in the Breda area. The contract will be through Undutchables

Our client is an international market leader in the pharmaceutical industry – focused on transforming science and biotechnology into therapies that have the power to restore health or save lives. The patients are the main priority at all times. This USA founded organization holds a large site in Breda, where produced medicines are labeled, stored and shipped worldwide, to more than 75 countries. The staff in Breda works on supply chain processes, engineering, clinical research, marketing and sales on a daily basis. The company culture is dynamic and fast paced, with a strong international character.