Job Description
The Manufacturing Process Technician plays a vital role in the smooth 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.
This 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 but not limited to operating and setting up manufacturing equipment, processing parts and components for manufacturing, performing transactions in electronic systems, and cleaning and sanitizing production areas.
This job specification outlines the general responsibilities associated with the role of Manufacturing Process Technician. The site focuses on continuous improvement of all work processes and practices, and colleagues are required to be flexible in this regard.
Please note that this is a Fixed Term Contract role for 24 months, and successful candidates will be required to work a shift pattern.
Required Skills and Qualifications
* Manufacturing process, packing, and inspection technicians are required to work a variety of shift patterns, including days, 2, 3, and 4 cycle shifts.
* They will perform all operations with due care and attention and in accordance with Good Manufacturing Practices and company requirements.
* They will be involved in problem-solving and troubleshooting, including initiation and documentation of investigations.
* They will be responsible for the performance of self-inspection Quality & Safety Audits within their functional area.
* They will participate in a learning and development program, which will include annual reviews and goal setting via the MAP process.
* They will be responsible for cross-training other colleagues.
* They will be responsible for the use, review, revision, and upgrade of operational documentation and peer review of operations.
* They will play a key role in the development of manufacturing systems and will be responsible for continuous improvement initiatives.
* They will be champions for safe working practices and safety initiatives within their functional area.
* They will carry out any sampling, testing, and inspections that may be required.
Benefits
* Results-oriented individuals with excellent organization, communication, and team development skills who can successfully interact with people and generate cooperation.
* Demonstrated ability to deliver to team, site, and personal objectives.
* Demonstrated understanding and use of RFT techniques and lean manufacturing concepts.
Others
* A third-level qualification in a relevant discipline would be an advantage.
* Applicants should have some relevant experience of operation of a manufacturing function in a sterile pharmaceutical manufacturing or similar environment.