We are looking for a Validation Engineer to join a Pharmaceutical Company in Dublin to lead the commissioning, validation and assembly documentation for a key project finalization. This is a 6 month hourly rate contract position.Key Responsibilities:Lead Commissioning, Qualification, and Validation (CQV) activities for assembly equipment.Manage and execute technical documentation to finalize the project lifecycle.Oversee calibration requirements and ensure compliance with site standards.Utilize strong Project Management skills to meet strict deadlines for project handover.Skill, Attributes, Experience:Minimum 3+ years experience in Validation/Commissioning ideally with a background in Pharmaceuticals or Medical Device.Bachelor's Degree in Engineering or a related technical field.Proven track record in assembly validation and calibration processes.Strong project management skills.Strong communication skills.