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.