3588
Production Operator
Carlow, Ireland
Life Science
Fix Term Contract
3588
Posted on:
October 7, 2024
The Highlights:
- Perform day to day laboratory testing & data review
- Work with leading edge technology
- Excellent professional development and progression opportunities
The Role:
Elusav Recruitment have an excellent opportunity with a leading global Pharma and Biopharma company who is seeking a Production Operator to bring value to their facility in Carlow.
As part of the IPT team, you will perform various production and operations related tasks as part of an empowered team to aid in the manufacture and reliable supply of product.
Job Responsibilities:
- Operate and/or monitor production activities and support equipment, using MES/DCS and PLC based systems, to ensure optimum equipment uptime and target outputs. Equipment will include, yet is not limited to, parts washers, autoclaves, portable tank CIP/SIP/storage panels, Vial Washer, Depyro Tunnel, Debagger and filling machines.
- Work collaboratively to drive a safe and compliant culture in Carlow. Clean room cleaning, housekeeping and materials management in all production areas while focusing on continuous process improvement using Lean Principles.
- Maintain process equipment, completing preventative maintenance and equipment troubleshooting and repairs where qualified to perform tasks.
- Participate effectively in writing/revising/ rolling out accurate operational procedures, training materials for various IPT systems; ensure all work is carried out in line with same. Support continuous improvement by active participation in investigations and investigation reports, execution/development of change control, and contribution to Kaizen events and projects as appropriate. Perform root cause analysis, using standard tools and methods, to resolve system issues e.g. FMEA, Fishbone diagrams, 5 why’s etc.; implement subsequent corrective action through the change management system.
- Required to comply with the company Global Policies, Procedures and Guidelines, regulatory requirements and execute current good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.
- Manage equipment flow, including tracking soiled and clean hold times, proper labeling and inventory management of clean and sterile equipment using Kanbans and automated MES system to set QC status and expiry of sterile equipment.
Job Requirements:
- Leaving Certificate or equivalent required.
- Apprenticeship, Certificate or Diploma preferred, ideally in a related discipline.
- Would typically have prior related work experience; ideally in a manufacturing, preferably GMP setting.
If you would like to learn more about the vacancy, apply now, or contact Stephen O'Brien on stephen@elusav.com or +3536959993.
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Production Operator
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