Quality Operations Specialist

About the role

Recordati is seeking a Quality Operations Specialist to ensure the implementation and sustainability of GMP, hygiene, and quality system requirements across its pharmaceutical sites. The role supports product release, deviation handling, and continuous improvement of quality processes.

Key responsibilities

• Implement and sustain GMP, hygiene, and quality system requirements.
• Manage product release by reviewing batch documentation and related records.
• Oversee deviation, customer complaint, product return, and CAPA processes, including reporting.
• Prepare Annual Product Quality Reviews, trend analyses, and quality performance metrics.
• Participate in internal and external audits and drive continuous improvement of quality systems.
• Conduct risk assessments, coordinate training activities, and manage quality documentation processes.

Required profile

• Bachelor’s degree in Chemistry, Chemical Engineering, or a related scientific discipline.
• 3‑4+ years of Quality Assurance experience in the pharmaceutical industry.
• Strong knowledge of GMP regulations and quality documentation systems.
• Fluent or professionally proficient English preferred.
• Completion of military service required for male candidates.
• Willingness to reside in or relocate to Çerkezköy, Kapaklı, Çorlu or Ergene.

Required skills

• GMP regulations knowledge.
• Quality documentation systems proficiency.
• Microsoft Office applications.
• Risk assessment methodology.
• CAPA management.
• Audit participation and reporting.