Manufacturing Process Technician
The Manufacturing Process Technician plays a crucial role in the operation and maintenance of manufacturing equipment.
This individual is responsible for monitoring and adjusting manufacturing processes, troubleshooting any issues, and ensuring the quality of final products. They work in compliance with company policies and safety regulations.
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. These roles include operating and setting up manufacturing equipment, processing parts and components for manufacturing, performing transactions in electronic systems, and cleaning and sanitizing production areas.
Key Responsibilities
* Operate and maintain manufacturing equipment
* Monitor and adjust manufacturing processes
* Troubleshoot issues and ensure product quality
* Work in compliance with company policies and safety regulations
Working Environment
The site is focused on continuous improvement of all work processes and practices. Colleagues are required to be flexible and may be asked to carry out additional work functions not described in this specification but associated with their role.
Hiring Requirements
* Manufacturing Process Technicians must work a variety of shift patterns, including days, 2, 3, and 4 cycle shifts
* They must perform 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 be responsible for 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 conduct peer reviews of 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 calibrate and maintain test equipment
* They will assist with corporate, FDA, HPRA auditors, and other regulatory bodies during company audits
Qualifications
* Educated to Leaving Certificate standard or equivalent (minimum five passes including English and Mathematics required)
* A third-level qualification in a relevant discipline would be an advantage
* Applicants should have some relevant experience of operating a manufacturing function in a sterile pharmaceutical manufacturing or similar environment
* Be a results-oriented person with excellent organization, communication, and team development skills
* Demonstrated ability to deliver to team, site, and personal objectives
* Demonstrated understanding and use of RFT techniques and lean manufacturing concepts
Preferred Skills
* Experience working with equipment utilized in the manufacture of parenteral products, 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