Supply Chain Junior

Real; Breda; On-site; EUR 45,000 - 65,000; Full time

Job summary

Amgen Breda, Netherlands, is seeking an Associate Supply Chain on a 1-year contract (40 hours per week), with 2 days per week on-site in Breda.

You will support reverse logistics, tracking and tracing, and distribution complaints across the EMEA region, ensuring compliance with GMP, GDP, and SOX regulations.

The role demands strong English, advanced communication, ERP experience, problem solving, and ability to collaborate with an international group; a Master’s or Bachelor’s degree is required.

Qualifications

• Master's or Bachelor's degree with two years of Supply Chain experience in a GMP and GDP-regulated industry.
• Ability to multitask and work with a diverse, international group.
• Advanced communication skills and strong written/oral English.
• Proficiency in computer skills and ERP experience.
• Experience with issue handling in a logistic environment; problem-solving oriented.
• Proactive self-starter who can manage workload and prioritise tasks.

Responsibilities

• Support daily operations related to reverse logistics, tracking and tracing, and distribution complaints across the EMEA region.
• Ensure compliance with third-party distribution complaints and returns meeting KPIs and regulatory requirements (SOX, GDP).
• Monitor and coordinate the return of Finished Drug Products (FDP) to Amgen sites, CMOs, or warehouses, including recalls.
• Provide tracking and tracing oversight for shipments under Global distribution Hub and collaborate with process owners.

Skills

Advanced communication

English fluency

Multitasking

Problem solving

Proactive mindset

Analytical skills

Quality focus

Education

Master's or Bachelor's degree

Tools

ERP systems

Job description

Job title: Associate Supply Chain
Breda, 2 days per week
1 year contract to start with
40 hours per week

Accountabilities

• Support daily operations related to reverse logistics, tracking and tracing, and distribution complaints throughout the EMEA region.
• Ensure compliance in managing third-party distribution complaints and returns while meeting the established key performance indicators (KPIs).
• Ensure compliance with SOX and GDP regulations.
• Attention to detail and a quality mindset in all activities determine the root causes of problems with limited scope and complexity.

Responsibilities

• Monitors and coordinates the return of Finished Drug Products (FDP) to Amgen Sites(ABR/ADL), CMO or Amgen Warehouses or LSP locations. Including re-calls.
• Log, investigate, and follow up on low-risk distribution complaints by coordinating with relevant stakeholders. Ensure that all records are accurately initiated and concluded within the designated timelines and in compliance with regulatory requirements.
• Support tracking and tracing activities for shipments under the Global distribution Hub, providing daily oversight and collaborating with the business process owner.
• Supports team and business with continuous improvements
• Represent the team during Stakeholder management meetings
• Participates in ABR internal and external audits as needed.
• Other duties may be assigned to you as required.
• Ensures Amgen's policies and procedures are followed to ensure complete compliance.
• Continuously seek opportunities for improvement and generate innovative ideas to enhance the quality of our services.
• Supports the achievement of our departmental and global goals and initiatives
• Master's or bachelor's degree with two years of Supply Chain experience in a GMP and GDP-regulated industry.
• Ability to multitask and work with a diverse, international group.
• Advanced communication skills
• Computer skills and ERP experience
• Experience with issue handling in a logistic environment
• Problem-solving skills
• 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.
• Understanding of GMP regulations, GDP guidelines, and SOX regulations.
• Lean Six Sigma certification is a plus.
• Critical thinking, problem-solving and analytical skills.
• Analyzes a problem by gathering and understanding all relevant information.
• Able to manage multiple responsibilities and priorities simultaneously, especially in a fast-paced environment with time constraints.
• Ability to maintain attention to detail.
• Able to work effectively with people from diverse cultures and adapt to different working styles.
• Communicate issues in a timely manner.
• Capable of planning and organising tasks and work responsibilities to achieve objectives.
• Quality-focused mindset.
• Skilled in reporting and technical writing skills.
• Understand basic supply chain concepts, manufacturing networks and key business metrics

Other:

• Expected to work from Amgen Breda, Netherlands office, at least 2 days per week.