Quality Assurance Specialist

About the Role

We are seeking a Quality Assurance Specialist to join a prominent pharmaceutical company located in County Waterford. This position plays a vital role in ensuring the manufacturing, storage, and packaging processes adhere strictly to current Good Manufacturing Practices (cGMP).

This is an initial contract position for 12 months with potential for extension.

Key Responsibilities

• Collaborate with the Quality Assurance team to maintain compliance with cGMP standards.
• Assist in developing and delivering GMP training programs.
• Prepare and review procedural documents and batch records.
• Conduct scheduled audits across various departments.

Qualifications and Experience

• Possession of a relevant degree in a scientific or allied discipline.
• Demonstrated experience in a similar quality assurance role within a GMP-compliant environment.
• Practical knowledge and application of cGMP regulations.

Additional Information

This role involves ensuring regulatory compliance, continuous improvement initiatives, and maintaining quality systems. Keywords include Quality Assurance, GMP, Pharmaceutical, Batch Documentation, Audits, Training Packages, and Regulatory Compliance.