Job Opportunity: QC Equipment Validation Specialist
Location: Dublin – Pfizer Grange Castle (On Site)
Contract: 12-month Fixed Term (Contingent)
Cpl, in partnership with our client Pfizer, are seeking a QC Equipment Validation Specialist to join the team in their Chemistry Departments at the state-of-the-art Grange Castle site in Dublin. This is an exciting opportunity to work in a world-class pharmaceutical environment on a 12-month fixed term contract.
Key Responsibilities
- Support equipment validation activities within QC Chemistry laboratories.
- Collaborate with cross-functional teams to ensure compliance with GMP and regulatory requirements.
- Execute validation protocols, review documentation, and maintain equipment validation lifecycle.
- Provide technical support and expertise during qualification and validation activities.
- Ensure adherence to Pfizer standards, quality procedures, and safety guidelines.
Requirements
- Bachelor’s degree in Chemistry, Life Sciences, Engineering, or related field.
- Previous experience in equipment validation or QC laboratory environment (pharma or GMP preferred).
- Knowledge of GMP regulations and validation practices.
- Strong problem-solving, documentation, and communication skills.
- Ability to work effectively in a fast-paced, team-oriented environment.
What We Offer
- Opportunity to work with a leading global pharmaceutical company.
- Gain experience in a highly regulated GMP environment.
- Competitive compensation for a fixed-term contract.
- Collaborative and innovative working culture.
Work Location: On Site – Pfizer Grange Castle, Dublin