Validation Engineer – GMP & Tech Transfer

PSC Biotech Corporation; Galway; Hybrid; EUR 60,000 - 80,000; Full time

Job summary

PSC Biotech is seeking a Validation Engineer in Loughrea, Ireland to execute and document validation activities for processes, cleaning, equipment, and analytical instruments. The role supports GMP-compliant operations and regulatory readiness.

You will collaborate with manufacturing, quality, engineering, and analytical teams to ensure robust validation programs, maintain SOP alignment, and assist in tech transfers and new product introductions.

Qualifications

• Degree in Engineering, Pharmaceutical Science, or related discipline.
• 2–4 years in validation within a GMP-regulated environment.
• Experience in process, cleaning, and equipment validation preferred.

Responsibilities

• Develop, execute, and document validation protocols and reports for processes, cleaning, equipment, and utilities.
• Ensure validation activities comply with GMP, regulatory guidelines, and internal procedures.
• Support technology transfers and new product introductions through validation activities.
• Maintain accurate and complete validation documentation in accordance with SOPs and regulatory requirements.
• Assist in updating and implementing validation-related SOPs under guidance of the Validation Team Lead.
• Ensure validation records are audit-ready and support inspections.
• Identify opportunities to improve validation processes and efficiency.
• Work with manufacturing, quality, engineering, and analytical teams to coordinate validation activities.
• Provide technical support during troubleshooting and investigations related to validation.

Skills

GMP knowledge

Documentation

Cross-functional teamwork

Validation methodologies

Troubleshooting

Quality compliance

Education

Engineering, Pharmaceutical Science, or related discipline

Job description

PSC Biotech is seeking a Validation Engineer in Loughrea, Ireland to execute and document validation activities for processes, cleaning, equipment, and analytical instruments. The role supports GMP-compliant operations and regulatory readiness.

You will collaborate with manufacturing, quality, engineering, and analytical teams to ensure robust validation programs, maintain SOP alignment, and assist in tech transfers and new product introductions.