Process Equipment Engineer
- Ireland
- Contract
- Full-time
- 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.
- Assist with management, engineering, process improvement, equipment reliability, and control system activities.
- Identify, plan, schedule, manage and communicate on production related projects to all affected stakeholders.
- Ensuring systems, equipment, and products operate at optimal levels and meet BU needs by preventing failures and maximizing uptime
- Analyse equipment failure data, conduct root cause analysis, develop and implement new procedures and processes to prevent reoccurrence
- Implement lean technologies such as standard work, visualisation boards.
- Support the BU by developing robust process and systems to ensure delivery of effective quality.
- Resolve technical issues in an effective & timely manner with the technical team to support operations.
- Drive continuous improvement and process efficiency programs, i.e., OEE, OPEX, RCA, RCM and productivity output for the BU.
- Manage external vendors and services for equipment and technology in the BU along with Manufacturing.
- Manage technical documentation, reports, files, logs and records for the BU.
- Assist with the trending, monitoring and reduction of repeat deviations associated with the equipment and technology in the BU. Generate and approve associated change controls and relevant protocols.
- Help support the BU during regulatory and compliance audits.
- Third level qualification in Mechanical, Electrical or Process Engineering 4+ years experience working in high volume automation pharmaceutical manufacturing environment performing a similar role.
- Detailed knowledge of regulatory requirements in a pharmaceutical GxP environment.
- Excellent documentation skills.
- Excellent digital literacy with experience using Maximo, One Vault, Quality software and Microsoft Office (Word, Excel, PowerPoint etc.).