Equipment Engineer

Progressive; Leiden; In loco; EUR 60.000 - 90.000; Tempo pieno

Descrizione del lavoro

Johnson & Johnson Innovative Medicine in Leiden seeks an Equipment Engineer to act as the technical expert for critical manufacturing equipment, ensuring GMP-compliant operations and continuous improvement of biopharmaceutical production processes.

You will collaborate with Operations, Engineering, Maintenance and Quality to improve equipment performance, prevent contamination risks and support introduction of new systems, with a strong focus on safety, quality and productivity.

Competenze

• BSc or MSc in bioprocessing, chemical engineering, microbiology or a related field.
• Experience within biopharmaceutical or biotech manufacturing environments.
• Knowledge of GMP and manufacturing processes.
• Strong analytical and problem-solving skills.

Mansioni

• Drive equipment reliability and continuous improvement initiatives
• Perform root cause analyses and resolve equipment-related issues
• Lead asset management activities and support long-term replacement planning
• Ensure GMP-compliant documentation and processes
• Support the implementation of new equipment and systems
• Contribute to contamination prevention and manufacturing excellence
• Collaborate with cross-functional teams to improve safety, quality and productivity

Conoscenze

Analytical thinking

Problem solving

Formazione

BSc or MSc in bioprocessing, chemical engineering, microbiology or related field

Descrizione del lavoro

For one of our Life Science clients, we are currently searching for an Equipment Engineer.

Do you have experience in biopharmaceutical manufacturing and a passion for driving process improvements? Join Johnson & Johnson Innovative Medicine in Leiden as an Equipment Engineer within the Primary Recovery Centre of Expertise. In this role, you will act as the technical expert for critical manufacturing equipment, ensuring reliable operations, GMP compliance, and continuous improvement of biopharmaceutical production processes. You will work closely with Operations, Engineering, Maintenance, and Quality teams to improve equipment performance, prevent contamination risks, and support the introduction of new systems.

Your responsibilities

• Drive equipment reliability and continuous improvement initiatives
• Perform root cause analyses and resolve equipment-related issues
• Lead asset management activities and support long-term replacement planning
• Ensure GMP-compliant documentation and processes
• Support the implementation of new equipment and systems
• Contribute to contamination prevention and manufacturing excellence
• Collaborate with cross-functional teams to improve safety, quality and productivity

What you'll bring

• bsc or msc in bioprocessing, chemical engineering, microbiology or a related field
• experience within biopharmaceutical or biotech manufacturing environments
• knowledge of GMP and manufacturing processes
• strong analytical and problem-solving skills