Validation Analyst (GMP)

Job Title: Validation Analyst (GMP)

Location: Athlone, Ireland
Contract Duration: 12-month
Pay Rate: €45 - €55 per hour
Working Structure: Monday - Friday, full-time, 2 days onsite.

A leading multinational pharmaceuticals company is looking for a Validation Analyst (GMP) to join their team in Athlone, Ireland. This role focuses on software systems testing and validation in a GMP Lab environment. As a Validation Analyst (GMP), you will play a crucial role in ensuring that all software systems and applications within the lab meet regulatory requirements and function as intended.

Key Responsibilities:

• Validation Support: Provide validation support for new releases and modifications to applications throughout the software development life cycle (SDLC).
• Test Case Management: Prepare validation plans, test cases, and validation summary reports, ensuring test scripts challenge functional requirements and demonstrate accurate software performance.
• Change Control: Review and approve change controls associated with validated systems and ensure documentation meets SOP standards.
• Collaboration and Communication: Act as a validation representative at project team meetings, communicate with team members, and provide feedback to management regarding timelines and resource constraints.
• Documentation and Compliance: Assist in the preparation and review of system documentation, manage testing environments, and address any PQ-related issues arising from audits.

Requirements:

• Educational Background: Bachelor's degree in Information Technology, Computer Science, or a related field.
• Experience: Minimum of 3 years in data validation or a related role, with a solid understanding of clinical trials operational processes and the software development life cycle (SDLC).
• Skills: Strong analytical skills, attention to detail, excellent communication abilities, and proficiency in Microsoft Office Suite and other data analysis tools.
• Teamwork: Ability to work in a team-oriented environment and manage multiple tasks concurrently.

If you are a detail-oriented Validation Analyst (GMP) with experience in GMP Lab settings and a strong understanding of clinical operations, apply now to join a dynamic team in the pharmaceuticals industry and make a difference in a leading company.