Manufacturing Process Technician - Amgen
  • Dublin, Leinster, Ireland
  • via BeBee.com
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Job Description

Manufacturing Process Technician at Amgen: Monitor and adjust manufacturing processes, troubleshoot issues, and ensure quality of final products in a sterile parenteral drug environment.

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.

  • Monitor and adjust manufacturing processes to ensure quality and efficiency
  • Troubleshoot issues and implement corrective actions
  • Ensure compliance with company policies and safety regulations
  • Work in a team environment to achieve manufacturing goals

The Manufacturing Process Technician reports to the Shift Manager and will be responsible for one or more of the following roles:

  • Operation and setup of manufacturing equipment
  • Processing of parts and components for manufacturing
  • Performing transactions in electronic systems
  • Cleaning and sanitization of production areas

The site is focused on continuous improvement of all work processes and practices. All colleagues are required to be flexible and adapt to changing circumstances.

The Manufacturing Process Technician will be involved in problem-solving and troubleshooting, including initiation and documentation of investigations. They will also be responsible for the performance of self-inspection Quality & Safety Audits within their functional area.

  • Proactively identify operational improvement opportunities or process-related issues
  • Escalate and follow up with area Senior Associate Tech Engineers for effective resolution and implementation
  • Champion safe working practices and safety initiatives within their functional area
  • Carry out sampling, testing, and inspections as required
  • Contribute and assist with Corporate, FDA, HPRA Auditors and other regulatory bodies during company audits

Qualifications:

  • Leaving Certificate standard or equivalent (minimum five passes including English and Mathematics required)
  • Third-level qualification in a relevant discipline would be an advantage

Preferred Skills:

  • Experience working with equipment utilised in the manufacture of parenteral products
  • Good mechanical aptitude
  • Excellent problem-solving skills
  • Ability to work in a team environment and on one's own initiative

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