Novartis zoekt een
Junior Maintenance Engineer
Baarle-Nassau, Netherlands
Job Description
40+ is the dedicated number of team members you would be joining at IDB (Advanced Accelerator Applications, Netherlands) whose mission is to bring new therapies to patients wordwide by producing radiopharmaceuticals for targeted radioligand therapy. IDB 's team embraces the culture of empowerment and team work.
Job purpose and Main Activities
The purpose of the Junior Maintenance Engineer is to ensure that the integrity and reliability of the equipment is up to standard. By ensuring that all maintenance activities are performed and documented according to our GMP and internal guidelines. This ensures a safe and reliable operation of the IDB production equipment.
• Execution of maintenance (with support of vendor in specific fields) in and outside the GMP production area.
o Corrective maintenance, including remediation of first-line failures
o Preventive maintenance, and helping in the preparation of planned stops
o Inspective maintenance, through execution of protocols as specified
o Calibration, per specified interval including documentation
• Partner with our manufacturing and quality team to set the right priorities and determine solutions for technical challenges.
• Controlling and administrating the spare parts for the production equipment in alignment with the Maintenance/Reliability Engineer
• Being a key partner in continuous improvement, providing input to equipment modifications and overall process based on maintenance activities (breakdowns, interruptions etc.)
• Supporting validation activities per the defined validation protocols
• Supporting the Maintenance/Reliability Engineer in preparing maintenance interventions
• Develop, revise & review related technical documents (Work-instructions, Job Plans, HECP’s etc.)
• Providing technical training to operators where needed
Job purpose and Main Activities
The purpose of the Junior Maintenance Engineer is to ensure that the integrity and reliability of the equipment is up to standard. By ensuring that all maintenance activities are performed and documented according to our GMP and internal guidelines. This ensures a safe and reliable operation of the IDB production equipment.
• Execution of maintenance (with support of vendor in specific fields) in and outside the GMP production area.
o Corrective maintenance, including remediation of first-line failures
o Preventive maintenance, and helping in the preparation of planned stops
o Inspective maintenance, through execution of protocols as specified
o Calibration, per specified interval including documentation
• Partner with our manufacturing and quality team to set the right priorities and determine solutions for technical challenges.
• Controlling and administrating the spare parts for the production equipment in alignment with the Maintenance/Reliability Engineer
• Being a key partner in continuous improvement, providing input to equipment modifications and overall process based on maintenance activities (breakdowns, interruptions etc.)
• Supporting validation activities per the defined validation protocols
• Supporting the Maintenance/Reliability Engineer in preparing maintenance interventions
• Develop, revise & review related technical documents (Work-instructions, Job Plans, HECP’s etc.)
• Providing technical training to operators where needed
Diversity & Inclusion / EEO
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Minimum Requirements
• MBO+ or HBO degree (Mechanical/ Electrical/ Mechatronic Engineering (MTS).
• Preferred qualifications: 2+ years of working experience within (pharmaceutical) GMP or isotope manufacturing
• Attention to safety, able to work in an organized and structured manner through protocols and standards
• Analytical skills and Analytical Trouble Shooting (ATS) approach
• Attention to detail, ability to look at the process through the eye of the end-user as well as an engineer
• Preferred qualifications: 2+ years of working experience within (pharmaceutical) GMP or isotope manufacturing
• Attention to safety, able to work in an organized and structured manner through protocols and standards
• Analytical skills and Analytical Trouble Shooting (ATS) approach
• Attention to detail, ability to look at the process through the eye of the end-user as well as an engineer