Job Title: Validation Officer (QC / GMP)
Location: Cookstown, Dublin 24 (Office-Based, Monday to Friday)
Job Type: Full-Time
Annual Leave: 20 Days
An exciting opportunity has become available for a Validation Officer to join a growing pharmaceutical team based in Cookstown, Dublin 24. This is an excellent role for candidates with an interest in analytical instrument validation, method verification, and GMP compliance, looking to develop their career in a regulated lab environment.

Key Responsibilities:

• Prepare and execute validation protocols (IQ/OQ/PQ) for lab instruments and analytical equipment.
• Perform analytical method validation and verification according to ICH and regulatory guidelines.
• Review and approve validation plans, risk assessments, and final reports.
• Conduct revalidation and periodic reviews as scheduled.
• Collaborate with cross-functional teams including QA, Engineering, and Production on validation activities.
• Ensure compliance of systems and equipment with 21 CFR Part 11 and data integrity standards.
• Maintain up-to-date, compliant validation documentation and traceability records.
• Support internal and external audits and contribute to validation-related audit responses.
• Investigate deviations and contribute to CAPA implementation relating to validation findings.
• Stay informed of industry best practices and regulatory updates in validation and lab compliance.

Skills & Competencies:

• Good understanding of cGMP, ICH, and relevant regulatory standards (FDA, EMA, etc.).
• Familiarity with validation protocols and data integrity principles.
• Strong documentation and organizational skills.
• Ability to manage time effectively and prioritize tasks.
• Detail-oriented with a commitment to quality and compliance.
• Team player with excellent communication and interpersonal skills.
• Proactive approach to learning and problem-solving.

Education & Qualifications:

• BSc (or equivalent) in a scientific discipline such as Chemistry, Pharmaceutical Science, or related field.
• Previous experience in a GMP or regulated lab environment is desirable but not essential—training provided.

If you’re eager to build a career in validation within a quality-focused environment, we encourage you to apply now!
Job Type: Full-time
Pay: €12.99-€15.14 per hour

Additional pay:

• Performance bonus

Benefits:

• On-site parking
• Sick pay

Schedule:

• Monday to Friday

Work Location: In perso

• Prepare and execute validation protocols (IQ/OQ/PQ) for lab instruments and analytical equipment.
• Perform analytical method validation and verification according to ICH and regulatory guidelines.
• Review and approve validation plans, risk assessments, and final reports.
• Conduct revalidation and periodic reviews as scheduled.
• Collaborate with cross-functional teams including QA, Engineering, and Production on validation activities.
• Ensure compliance of systems and equipment with 21 CFR Part 11 and data integrity standards.
• Maintain up-to-date, compliant validation documentation and traceability records.
• Support internal and external audits and contribute to validation-related audit responses.
• Investigate deviations and contribute to CAPA implementation relating to validation findings.
• Stay informed of industry best practices and regulatory updates in validation and lab compliance