Logistics Process Engineer

Are you an analytical logistics expert with a passion for process optimization and strict quality assurance within a pharmaceutical environment? As a Logistics Process Engineer at our client, you will take ownership of raw material supply flows and distribution processes. In this role, you will analyze and streamline logistics workflows across the Janssen Biologics warehouse and distribution center. Working closely with cross-functional teams, you will identify bottlenecks, implement process enhancements, and ensure full compliance with regulatory standards (GMP).

Process Analysis & Optimization: Conduct thorough evaluations of existing logistics processes and workflows to eliminate inefficiencies, mitigate risks, and resolve operational bottlenecks.

Quality & Technical Writing: Develop, review, and maintain Standard Operating Procedures (SOPs), work instructions, and quality documentation in strict compliance with GMP guidelines.

Stakeholder Collaboration: Partner closely with the distribution center, warehouse management, local operations, QA (Quality Assurance), and Global Planning teams to ensure end-to-end alignment.

Technology & Systems: Evaluate and utilize logistics software and tools (such as SAP, WMS, and Salesforce-based applications) to optimize daily operations.

Performance Tracking (KPIs): Define, monitor, and report key logistics metrics to continually assess performance and drive data-driven improvements. Apply now and receive a WhatsApp message within 15 minutes with a few short questions, so we can help you quickly. Don't have WhatsApp? We'll contact you by phone or email!

Job requirements: Education|Experience: Bachelor’s degree in Logistics, Supply Chain Management, Industrial Engineering, or a related field.; and minimum 3 years of proven experience in process improvement, supply chain optimization, or a similar role within the pharmaceutical or logistics industry.

GMP Knowledge: Strong understanding of and hands-on experience in a highly regulated GMP environment.

Technical Writing: Meticulous attention to detail in writing and updating SOPs and compliance documentation.

Language Skills: Proficient verbal and written communication in English. Good understanding of the Dutch language is a preferred plus.

Competencies: Strong analytical and problem-solving mindset, Excellent technical writing skills and high attention to detail, Effective communication and stakeholder management capabilities, Adaptability in a fast-paced, high-standard environment, Proactive approach to process improvement and ownership.

Terms of employment: A contract for a year (with possibility of extention) for 32 to 40 hours per week, A monthly project allowance 4% of your salary, 25 holiday days, 8% Holiday Pay, A travel allowance, A good pension scheme, Extra allowances for a home workplace budget, A training budget, coaching, an onboarding program, and unlimited access to the Randstad Academy with over 3,000 courses and trainings, Networking events and knowledge sessions.

Information about the company: The client in Leiden is a global leader in the development and production of innovative vaccines and biological medicines. Within the Engineering, Validation & Maintenance (EVM) department, you will step into a professional environment where collaboration, quality, and safety are paramount. As a consultant through Randstad Professionals, you will have the opportunity to apply your expertise within this high-tech GMP environment.

You will work closely with driven domain experts and directly contribute to impactful change initiatives.

Good to know: You'll receive a WhatsApp message from us within 15 minutes of applying. We'll ask you a few short questions about your application to help you more quickly. Don't have WhatsApp? No problem! We'll contact you by phone or email.