Description

You will design, troubleshoot, and optimize automation systems for radiopharmaceutical production.

This role is on-site.

Responsibilities

• Design and optimize automation systems for radiopharmaceutical manufacturing processes.
• Integrate and validate IT/OT systems with manufacturing execution systems (MES).
• Ensure all automation processes comply with 21 CFR Part 11 and GMP regulatory standards.
• Support validation and technical documentation of automation processes.
• Troubleshoot existing automation and systems engineering workflows.

Required Skills

• 3+ years of automation engineering experience in pharmaceuticals or radiopharmaceuticals.
• Hands-on experience with Comecer Isolators (Hot Cells).
• Proficiency in PLC, SCADA, and DCS systems (DeltaV, Siemens, Rockwell).
• Direct experience with IT/OT integration within GMP environments.
• Proven experience with manufacturing software integration (MES, SCADA, ERP).
• Background in Systems Engineering or Process Engineering.
• Strong understanding of data integrity and alarm management protocols.
• Experience working within the radiopharmaceutical industry.

Preferred Skills

• Bachelor's degree in Engineering or a related field.

Key Skills

Education

Bachelor's degree