Validation Engineer - County Sligo, Ireland - 6-Month Contract
Located on the picturesque west coast of Ireland, our global pharmaceutical client is seeking a Validation Engineer to join their state-of-the-art pharmaceutical facility.
Situated in the historic province of Connacht, near the Atlantic Ocean, the area offers a blend of Irish culture and modern living in a popular seaside town filled with bars, restaurants, and water sports.
Responsibilities:
1. Ensure all computerized systems are qualified in compliance with Data Integrity policies and regulatory requirements.
2. Coordinate, direct, and actively participate in the validation of site equipment, facilities, utilities, processes, and software in compliance with company policies, FDA, European cGMP, and GAMP standards.
3. Generate and maintain Validation Master Plans.
4. Create and update Project Validation Plans.
5. Develop validation plans, protocols, and final reports to cGMP standards.
6. Review and approve all protocols and final reports.
7. Manage the validation change control process.
8. Adhere to and support all EHS & E standards, procedures, and policies.
Requirements:
1. Third-level qualification in a relevant engineering or scientific discipline.
2. A minimum of 5-10 years’ experience in a cGMP regulated environment.
3. Strong understanding of regulatory requirements.
4. High attention to detail and concentration to ensure accuracy and compliance.
5. Proven problem-solving skills and adaptability to new regulatory requirements.
6. Innovative thinking with the ability to propose, demonstrate, and implement new solutions regularly.
If this role interests you, please apply now!
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