FIND_THE_RIGHTJOB.
JOB_REQUIREMENTS
Hires in
Not specified
Employment Type
Not specified
Company Location
Not specified
Salary
Not specified
Job Responsibilities:
Lead the planning and coordination of domestic and international plasma shipments ensuring
compliance with SOPs, GMP, and regulatory requirements.
Oversee end-to-end logistics operations including inventory planning, Inventory Management route
forecasting, documentation, customs clearance, and transportation efficiency.
Ensure Business and operational planning aligns with organizational goals and demands.
Hire, Train and Supervise logistics, Planning and inventory teams, ensuring accountability,
performance standards, and adherence to company policies.
Develop KPIs and dashboards to monitor logistics performance, carrier reliability, and inventory
movements.
Ensure timely execution of mitigation actions in case of logistics deviations and communicate
updates to stakeholders.
Collaborate with QA and Regulatory Affairs to ensure documentation, licensing, and inspection
readiness.
Support the creation and maintenance of SOPs and work instructions related to logistics and
planning activities.
Manage logistics-related budgets and ensure alignment with operational needs and forecasts.
Participate in audits and prepare necessary documentation, data, and responses for internal and
external inspections.
Identify areas for process improvement, implement best practices, and drive a culture of continuous
improvement.
Any roles or responsibilities may be changed based on the business needs.
Participate in the physical count of Inventory as per top management Instructions.
Professional experience required
Bachelor's degree in Pharmaceutical, Business Administration, Supply Chain Management,
Engineering, or a related field.
Minimum 7 years of experience in logistics, planning, or supply chain management, including at
least 2 years in a leadership role.
Strong working knowledge of pharmaceutical logistics, temperature-controlled transport, and
regulatory environments (e.g., cGMP, WHO, FDA, EU, EDA).
Demonstrated ability to lead teams, manage projects, and work under pressure in a regulated
industry.
© 2026 Qureos. All rights reserved.