The Manufacturing Process Technician reports to the Shift Manager and will be responsible for one or more of a number of roles relating to the manufacture and Inspection of sterile parenteral drugs
Job Summary
The Manufacturing Process Technician reports to the Shift Manager and will be responsible for one or more of a number of roles relating to the manufacture and Inspection of sterile parenteral drugs.
They will be involved in problem solving and troubleshooting including initiation and documentation of investigations, and will be responsible for the performance of self-inspection Quality & Safety Audits within their functional area.
They will play a key role in the development of the manufacturing systems and will be responsible for continuous improvement initiatives, proactively identifying operational improvement opportunities or process related issues.
Matching Summary
The Manufacturing Process Technician reports to the Shift Manager and will be responsible for one or more of a number of roles relating to the manufacture and Inspection of sterile parenteral drugs.
Skills & Requirements
Must-have
Operation and set up of manufacturing equipment
Processing of parts and components
Performing transactions in electronic systems
Cleaning and sanitization of production areas
Good Manufacturing Practices (GMP) compliance
Problem solving and troubleshooting
Self-inspection Quality & Safety Audits
Nice-to-have
Continuous improvement initiatives
Champions for safe working practices
Cross training of other colleagues
Results-oriented person
Excellent organization and communication skills
Ability to create a team environment
Key Requirements
Educated to Leaving Certificate standard or equivalent
Third level qualification in a relevant discipline would be an advantage
Relevant experience in sterile pharmaceutical manufacturing
Demonstrated understanding and use of RFT techniques
Demonstrated understanding and use of lean manufacturing concepts