Process Validation Co-Op

Location: hirify.global Manufacturing, Castlebar, County Mayo, Ireland; full-time and onsite

Company

hirify.global is a global healthcare manufacturing organisation focused on vital organ therapies, kidney care, dialysis services, and digital healthcare solutions.

What you will do

• Learn and support the process validation lifecycle in a regulated manufacturing environment.
• Prepare process validation protocols and participate in protocol execution and report writing.
• Assist with equipment qualification, validation test cases, sample collection, and periodic reviews.
• Manage, track, and execute validation documentation using site validation software and electronic systems.
• Collaborate with Quality, Technical, Engineering, Manufacturing, and other cross-functional stakeholders.
• Contribute to plant-critical and strategic validation projects.

Requirements

• Current studies in Pharmaceutical Science, Process Validation, Quality Assurance, or another relevant scientific discipline.
• Interest in process validation, quality systems, manufacturing operations, and regulated pharmaceutical environments.
• Ability to complete a full-time onsite placement in Castlebar, County Mayo.
• Willingness to complete quality, safety, compliance, validation systems, and relevant Grade C training where required.

Culture & Benefits

• Six-month placement or longer with paid practical experience.
• Structured onboarding and job-specific training.
• Side-by-side mentoring from a trained Process Validation Engineer.
• Experience with validation systems and electronic tools, including VMS, SRD, and TcU.
• Opportunity to build technical, organisational, planning, and communication skills in a regulated healthcare manufacturing environment.