Technical Engineer

Technical Engineer: SY3

Location: Ireland - Dublin & Kerry client Sites 

Rate: €500 - €600 p/d

Role definition & requirement:-

Technical Project Services Engineer with windows server background and desk side knowledge and technical authorship skills

Must have GxP Compliance experience working in a Pharmaceutical controlled Manufacturing plant aligned to EMEA and FDA regulations. Daily face to face interaction with the Client who resides in same office.

Must be able to travel between Dublin and Kerry sites (4 hours by car) with possible travel to Meppel, NETH also.

Compliance with AICL SOPs, Policies and Guidelines
Compliance with GmP / GdP / GxP

• Provide day to day support to Solutioners and Project Managers for RFS solutioning in the engagement phase and project delivery in the execution stage ensuring that all Manufacturing stipulations and best practice are adhered to - critical part of this role
• Provide input into the Design Process at the Manufacturing Plants
• Generate / update all Compliance documentation in accordance with AICL regulatory standards - critical part of this role - technical documentation / authorship must be at an outstanding level
• Provide support for locally controlled on-site servers; build, backup, restore
• Provide support for onsite printers, local and networked
• Provide support for IT Peripherals
• Provide support for all network / cabling / switches / hubs / CAT and Voice
• Assign service requests / incident tickets to the service desk

Available and flexible to work OOH in line with any Plan shut downs and Change Windows so as to not impact the Production Lines for drug manufacturing Background on Customer and why our Resource Requirements are Unique / Challenging To Find and Retain
Unique in that it's a Global Contract, FDA regulated Pharmaceutical environment, everything we do has to be qualified via the GxP / GDP practices.

Three manufacturing plants in Meppel, Dublin and Kerry - different QA compliance process on each site as different stages of manufacturing take place.

Resources need to be on-site in IRE, have a Pharma background, be onboarded to manufacturing plant standards, be compliance trained and retained to build up GxP skills / knowledge base, co-located with Client so excellent relationship building and comms skills.

Require resource who can travel between the 2 sites - approx 4 hours by car.