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Senior QC Associate
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Republic of Ireland
Manufacturing Technician
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Details
Production Operator
Reference: | AS21876 | Location: |
Carlow |
Qualification: | Certificate | Experience: | See description |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
May be suitable for:
Occupational Hygienist, Production Engineer, Production Planner, Production Support Engineer
Production Operator
11 Months
Carlow
AS21876
We’re currently recruiting for an exciting opportunity with a Pharmaceutical organisation based in Carlow.
As part of the IPT team, perform various production and operations related tasks as part of an empowered team to aid in the manufacture and reliable supply of product. Ensure that objectives are effectively achieved, consistent with company’s 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 labelling 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.
- Leaving Certificate, Apprenticeship, or Diploma preferred, ideally in a related discipline.
- Prior related work experience; ideally in a manufacturing, preferably GMP setting.
- Sterile filling processes and equipment experience beneficial.
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Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
This site uses cookies. More information on cookies can be found in our Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328
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