Equipment Engineer - GMP Biopharma & Process Improvement

Tandem Project Management Limited; Dublin; On-site; EUR 70,000 - 95,000; Full time

Job summary

Tandem Project Management Limited is seeking an Equipment Engineer for a leading biopharmaceutical company in Dublin. The role provides technical support to production and maintenance, with ownership of drug substance process equipment and compliance with GMP, safety and regulatory requirements.

You will lead troubleshooting, support installation and commissioning, oversee maintenance planning, drive equipment reliability, and partner with site functions to ensure readiness and continuous

Qualifications

• Degree in Pharmaceutical, Chemical or Mechanical Engineering or related discipline is required.
• Demonstrated ability in vendor management and resolving issues.
• Knowledge of regulatory requirements and health and safety legislation is essential.

Responsibilities

• Drive continuous improvement across engineering teams.
• Lead complex troubleshooting and structured problem-solving relating to process equipment.
• Provide technical support during installation and commissioning of new equipment.
• Oversee maintenance job plans and spare parts identification for operational readiness.
• Collaborate with site functions to ensure smooth transition from project to operations.
• Provide equipment design input for new product introductions and related capital projects.
• Lead investigations into process safety and equipment issues and implement improvements.
• Develop and deliver technical training related to process equipment.
• Monitor KPIs to support process optimisation and maintain GMP compliance.

Skills

Vendor management

Structured problem-solving

Issue resolution

Regulatory knowledge

Education

Degree in Pharmaceutical, Chemical or Mechanical Engineering, or a related engineering discipline

Job description

Tandem Project Management Limited is seeking an Equipment Engineer for a leading biopharmaceutical company in Dublin. The role provides technical support to production and maintenance, with ownership of drug substance process equipment and compliance with GMP, safety and regulatory requirements.

You will lead troubleshooting, support installation and commissioning, oversee maintenance planning, drive equipment reliability, and partner with site functions to ensure readiness and continuous