Are you interested in taking the next step in your career with a global leader in medical devices and healthcare? Are you ready to challenge yourself and lead initiatives in a fast‑paced environment? Do you have a background in life sciences? You could be the perfect candidate for this opportunity! Don’t hesitate, apply today!
Job Description
Our client in Tipperary is seeking an experienced Senior Engineer to lead initiatives on‑site that are primarily focused on equipment and systems across packaging, sterilisation and shipping processes. A minimum of 5 years of engineering experience in a regulated manufacturing environment is required for this senior role.
Key Responsibilities
Lead engineering initiatives with a strong focus on the full equipment and systems validation lifecycle (IQ/OQ/PQ) across packaging, sterilisation and shipping processes, ensuring alignment with internal procedures and regulatory standards.
Evaluate, select and implement new equipment, technologies and processes through rigorous research, analysis and application of engineering best practices.
Manage backend operations – including packaging, sterilisation and shipping – to meet production targets and maintain seamless supply‑chain performance.
Drive automation and digitalisation projects to enhance operational efficiency, reliability and compliance.
Support product and process validation activities, including documentation development and execution of qualification protocols.
Collaborate on new product introductions and technology transfers, ensuring smooth integration into existing manufacturing systems.
Identify and lead process improvement initiatives using Lean, Six‑Sigma or equivalent methodologies to reduce waste and optimise performance.
Review and contribute to technical documentation, change controls, reports and memos to support continuous improvement and knowledge transfer.
Provide hands‑on technical leadership and mentorship to junior engineers and technicians, fostering a culture of learning and accountability.
Ensure full compliance with GMP, FDA, BSI, EEO regulations and internal quality systems, supporting audits and inspections as required.
Actively participate in cross‑functional teams, working closely with Quality, Regulatory Affairs, Operations and Supply Chain to deliver business‑critical outcomes.
Key Requirements
Bachelor’s degree in Mechanical, Manufacturing or Biomedical Engineering (Level 8 preferred).
Minimum five years’ experience in a regulated manufacturing environment (MedTech or pharma).
Proven experience in at least two or more of the following: Packaging, Sterilisation, Shipping, Automation, Validation, Process Improvement, Product Launches.
Strong understanding of GMP, validation protocols and risk management.
Hands‑on experience with equipment troubleshooting, process optimisation and documentation.
Familiarity with technical writing, including protocols, reports and SOPs.
Benefits
Competitive and attractive employee compensation package
Pension contributions
Health insurance
Paid public holidays
Location
Clonmel, Ireland | onsite
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