Job description
Qualification and Validation Engineer
Location: Waterford | 12-Month Contract | Pharmaceutical Manufacturing
We are hiring a Qualification and Validation Engineer to support new product introductions, equipment qualification, and site requalification activities within a regulated pharmaceutical environment. This is a 12-month temporary contract ideal for someone with strong technical expertise and a passion for quality and compliance.
What You'll Do:
- Design, execute, and report on validation studies for equipment, systems, and processes
- Ensure compliance with cGMP, FDA, and EU validation standards
- Support site change control and participate in regulatory inspections
- Maintain validation documentation throughout the lifecycle
What You Bring:
- 3-5 years' experience in healthcare or pharmaceutical manufacturing
- Degree in Science or Engineering (Chemistry, Microbiology, Pharmacy, or related)
- Strong knowledge of validation regulations, GAMP, ISPE, and quality systems
- Excellent communication, problem-solving, and project execution skills
Join a collaborative team driving quality and innovation in pharmaceutical manufacturing.
To apply, please email your CV to [email protected]
