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.
