Job Title: Manufacturing Process Technician
The Manufacturing Process Technician plays a crucial role in the operation and maintenance of manufacturing equipment.
Key Responsibilities:
* Monitor and adjust manufacturing processes
* Troubleshoot any issues
* Ensure the quality of final products
Job Description Summary:
The Manufacturing Process Technician reports to the Shift Manager and will be responsible for one or more roles relating to the manufacture and inspection of sterile parenteral drugs, including operating and setting up manufacturing equipment, processing parts and components, performing transactions in electronic systems, and cleaning and sanitizing production areas.
Work Environment:
This is a Fixed Term Contract role for 24 months. The successful candidate will be required to work a shift pattern.
Hiring Requirements:
* Manufacturing Process, Packing and Inspection Technicians must work various shift patterns, including days, 2, 3, and 4 cycle shifts.
* They must perform all operations with due care and attention and in accordance with Good Manufacturing Practices and Amgen requirements.
* They will be involved in problem-solving and troubleshooting, including initiation and documentation of investigations.
* They will perform self-inspection Quality & Safety Audits within their functional area.
* They will participate in a learning and development program, including annual reviews and goal setting via the Maximizing Amgen Performance (MAP) process.
* They will be responsible for cross-training other colleagues.
* They will review, revise, and upgrade operational documentation and peer-review operations.
* They will contribute to the development of manufacturing systems and implement continuous improvement initiatives.
* They will champion safe working practices and safety initiatives within their functional area.
* They will carry out sampling, testing, and inspections as required, and calibration and maintenance of test equipment.
* They will assist with Corporate, FDA, HPRA Auditors, and other regulatory bodies during company audits.
* They will carry out any other duties designated by supervisor/management from time to time.
Qualifications:
* Leaving Certificate standard or equivalent (minimum five passes, including English and Mathematics).
* A third-level qualification in a relevant discipline would be an advantage.
* Relevant experience in a sterile pharmaceutical manufacturing or similar environment is required.
* Results-oriented individuals with excellent organization, communication, and team development skills are preferred.
* Ability to deliver team, site, and personal objectives.
* Understanding and use of RFT techniques and lean manufacturing concepts.
Preferred Skills:
* Experience working with equipment used in parenteral product manufacture, such as Automated visual Inspection, filling lines, and formulation vessels.
* Good mechanical aptitude.
* Excellent problem-solving skills.
* Ability to work in a team environment and on one's own initiative.