The Company
Our esteemed pharmaceutical client excels in healthcare, prioritizing research, and innovation across various medical fields like mental health, neurology, anesthesia, gastroenterology, mycology, HIV/AIDS, allergies, and oncology.

Role Description
The role involves defining and solving problems, analyzing root causes, managing projects, conducting financial analyses, and improving efficiency. It also requires direct collaboration with other Mentor functional groups to meet goals within GMP/ISO compliance and address product design changes effectively.

Responsibilities
– Manages and executes medium-complexity projects, ensuring safety, regulatory compliance, and meeting company standards and business needs.
– Leads project planning and structure effectively, optimizing processes, equipment utilization, downtime, waste reduction, budget management, and capital investment in an innovative manner.
– Provides technical support to Production, addressing process deficiencies, changes, and equipment failures, and actively seeks improvements.
– Supports manufacturing in troubleshooting equipment issues and follows SOPs, GMPs, and regulations.
– Revises and maintains engineering, equipment, and process procedures, participating in GMP audits.

Requirement
– Bachelor's degree in Engineering with 2-4 years of experience in process or maintenance engineering, preferably in a medical devices environment.
– Proficient in project management, basic computer skills, and software applications (MS Office, MS Project Management, PowerPoint, Word, Excel, Outlook, Minitab).
– Experience in manufacturing environment and developing manufacturing standards.
– Proficient in Dutch and/or English.

Other Information
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