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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, this location blends Irish culture with modern amenities in a seaside town known for its vibrant bars, restaurants, and water sports.
Responsibilities:
* Ensure all computerized systems are qualified in compliance with Data Integrity policies and regulatory requirements.
* Coordinate, direct, and actively participate in the validation of site equipment, facilities, utilities, processes, and software in accordance with company policies, FDA, European cGMP, and GAMP standards.
* Generate and maintain Validation Master Plans.
* Develop and oversee Project Validation Plans.
* Create validation plans, protocols, and final reports adhering to cGMP standards.
* Review and approve all validation protocols and final reports.
* Manage validation change control processes.
* Support and adhere to all EHS standards, procedures, and policies.
Requirements:
* Third-level qualification in a relevant engineering or scientific discipline.
* Minimum of 5-10 years’ experience in a cGMP-regulated environment.
* Good understanding of regulatory requirements.
* High attention to detail and concentration to ensure accuracy and compliance.
* Proven problem-solving skills and adaptability to new regulatory requirements.
* 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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