Automation & Manufacturing IT Systems Engineer
Job Type | Fixed Term |
Location | Cork |
Area | Cork |
Sector | IT/Software |
Start Date | |
Advertiser | Darcy Ainscough-Denton |
Telephone | 01 574 6266 |
Job Ref | 1003249 (2) |
Job Views | 340 |
- Description
Team Horizon is seeking an Automation & Manufacturing IT Systems Engineer (12-month fixed-term contract) for our client’s site in Cork, which is modern ‘bulk tablet’ facility manufacturing solid and capsule formulations for key therapeutic areas such as oncology and virology.
In this role you will work with counterparts in Production, QA, and Engineering departments and as a team, you will be responsible for all manufacturing Automation & IT systems/processes in use.
Why you should apply:
- This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
- There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
- Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.
What you will be doing:
- To administer and support all Automation & IT Processes in Pharmaceutical Manufacturing environment.
- Implement, qualify, commission and maintain manufacturing Automation & IT systems (MES, SCADA) and associate IT infrastructure that delivers operational efficiency and agility.
- Identify, evaluate and implement opportunities for continuous Automation & IT process improvement.
- Define requirements on capital projects and interact with internal & external stakeholders, vendors and contractors.
- Manage Automation projects throughout the project lifecycle.
- Work with Production/Engineering and Quality to troubleshoot and optimise output, minimise contamination and minimise costs.
- Generate & Maintain documentation (SOP’s & Technical Documentation) for full cGMP validation and operation, including documentation of changes made.
- Maintain Data Integrity Program, including remediation of legacy systems to ensure robust procedure and systems are in place covering data integrity, security and recovery.
- Actively Contribute to the Automation Business Strategy.
- Any other duties as assigned.
What you need to apply:
- Relevant 3rd level degree in Mechatronics, Electronics or Computer Technology.
- 3-4 years in a similar role in the Life Sciences environment.
- Experience working on PLCs (Siemens), SCADA (iFix, WinCC), Control Architecture and process equipment.
- Experience working on large-scale projects in Life Sciences generating, reviewing and approving lifecycle documentation.
- Building relationships with key stakeholders across the business.