Validation Officer

To perform validation and qualification activities for equipment, utilities, processes and systems, ensuring compliance with GMP, quality standards and approved procedures.

Validation & Qualification

• Perform validation activities in accordance with GMP requirements, approved protocols, and established procedures, actively participating in execution to identify limitations, assess potential improvements, and identify opportunities for process optimization.
• Conduct operational and performance qualification of equipment, utilities and processes.
• Investigate validation results, recommend improvement actions and perform re-tests where required.
• Maintain the validated status of equipment and processes.

Requalification

• Assess equipment and utilities for requalification requirements.
• Plan and perform requalification activities according to approved procedures.
• Daily oversight of manufacturing activities and verification of adherence to validated/qualified requirements.

Planning & Operational Support

• Provide technical support on validation-related activities.
• Identify gaps and recommend improvements to processes and procedures.
• Support changes and improvements to equipment, processes and systems.

Documentation & Reporting

• Maintain accurate validation documentation and records.
• Prepare validation reports and ensure they are completed within required timelines.
• Ensure validation records are stored and maintained in accordance with QMS requirements.

Qualification:

• N4-N6 / Trade Tested Artisan with 2-4 years' relevant experience

Experience:

• Relevant Science/Engineering qualification with pharmaceutical or equivalent industry experience.
• Experience in pharmaceutical manufacturing, equipment or process validation is advantageous.

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