AIQ Engineer

Overview

We are looking for a proactive and meticulous AIQ Engineer to be part of our Quality Control Laboratory team located in Cork, Ireland. This full-time, on-site position is pivotal in maintaining the reliability and regulatory compliance of Laboratory Systems supporting pharmaceutical production.

Key Responsibilities

• Collaborate with ELM team members to deliver IT components for laboratory capital projects.
• Create, review, and approve documentation related to laboratory systems.
• Coordinate with site teams to gather requirements and develop configuration specifications as well as IOQ test protocols.
• Participate in risk assessments to identify and mitigate potential issues.
• Deploy system content and provide training to end users.
• Demonstrate understanding of quality control’s critical role in pharmaceutical manufacturing by performing tasks with high integrity.
• Adapt and deliver additional related duties as needed.

Requirements

• Experience in supporting IT applications is essential.
• Familiarity with 21CFR Part 11 regulations and data integrity guidelines is preferred.
• Knowledge of Microsoft Windows Operating Systems including Windows 10, 11, and server variants.
• Prior exposure to QC laboratory systems support is advantageous but not mandatory.
• Strong problem-solving aptitude with excellent verbal and written communication capabilities.
• Exceptional organizational skills including time management and prioritization.
• Ability to work independently and collaboratively within a team.
• Pharmaceutical industry experience is a plus.

Additional Information

The candidate must possess strong interpersonal skills to foster effective cross-functional relationships both inside and outside the laboratory environment. Integrity and attention to detail are crucial in line with the importance of quality control in pharmaceutical manufacturing.