We are seeking an experienced commissioning engineer to support pharmaceutical and biopharmaceutical projects. You’ll work both remotely and on-site with clients, ensuring equipment and process systems are correctly commissioned, qualified, and performing as required.

Key Responsibilities

Install, commission, and execute IQ/OQ, cycle development, and customer training.
Complete project administration, including reports, expenses, and timesheets.
Communicate effectively with customers, suppliers, and internal teams.
Manage test and company equipment responsibly on-site.
Contribute to design qualification and continuous improvement.
Troubleshoot and provide technical support to customers and colleagues.
Carry out preventive maintenance, calibration, and technical support.
Prepare and manage servicing, calibration, and spare parts documentation.
Participate in FAT and customer meetings.
Support training of junior engineers.

Skills and Experience

Strong technical writing and clear documentation skills.
Experience with autoclaves, equipment validation, or instrument calibration.
Knowledge of validation systems (e.g., E-Val Pro or similar; training can be provided).
Degree or equivalent in Engineering, Science, or Validation.
Ability to read technical drawings, process specifications, and safety protocols.
Solid understanding of equipment validation lifecycles in pharma.
Proven ability to manage multiple projects and meet deadlines.
Strong analytical and organisational skills with excellent attention to detail.
Excellent communication and presentation skills with customers and suppliers.
Proficient in Microsoft Office.
Self-motivated, adaptable, and able to work independently.
Must be willing to travel and stay away from home for extended periods (UK, Ireland, EU, and occasionally further afield, as required).

Should you be interested in learning more please apply directly and or send your cv to [email protected]. Candidates must have the legal right to work in Ireland and the UK at the time of application.