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Rachel Kent
Life Science

+353 87 427 8808
[email protected]
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Details

Production Operator


Reference:RK21876 Location: Carlow
Qualification:CertificateExperience:1-2 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Production Planner

Production Operator
RK21876
Contract – 11 months
Carlow



We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.



As part of the IPT team, perform various production and operations related tasks aspart of an empowered team to aid in the manufacture and reliable supply of product. Ensure thatobjectives are effectively achieved, consistent with requirements to ensure compliance,safety and reliable supply to our customers.


Duties:

  • 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
  • Clean room cleaning, housekeeping and materials management in all production areas while focusing on continuous process improvement using Lean Principles.
  • 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.
  • 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 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.
  • Work collaboratively to drive a safe and compliant culture in Carlow.
  • May be required to perform other duties as assigned.


Experience and Education:
  • 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 interested in this posting please feel free to contact Rachel Kent on +353 (0)87 427 8808 or [email protected] for further information.