Quality Systems Specialist

About the role

Recordati is seeking a Quality Systems Specialist to support its pharmaceutical manufacturing operations in Turkey. You will ensure compliance with GMP, Ministry of Health regulations, and the company’s Quality Management System while fostering a strong quality culture.

Key responsibilities

• Execute Quality Assurance activities in line with GMP and local regulations.
• Plan, coordinate, and document validation and qualification studies, including process, cleaning, and transportation validation.
• Prepare, review, and control quality documentation such as SOPs, protocols, and reports.
• Manage Change Control, Deviations, CAPA, risk assessments, and Quality Agreements.
• Participate in internal, external, regulatory, and supplier audits and follow up on corrective actions.
• Coordinate supplier qualification and ensure cross‑functional compliance.
• Develop and monitor Validation Master Plans and oversee re‑validation needs.
• Deliver GMP and Quality Assurance training to promote continuous improvement.

Required profile

• Bachelor’s degree in Chemistry, Chemical Engineering or a related scientific discipline.
• 3‑4+ years of QA experience in the pharmaceutical industry.
• Strong knowledge of GMP regulations and quality documentation systems.
• Professional proficiency in English.
• Male candidates must have completed military service.
• Willingness to reside in or relocate to Çerkezköy, Kapaklı, Çorlu or Ergene.

Required skills

• Microsoft Office applications
• GMP regulatory knowledge

What we offer

• Opportunity to work in a global, purpose‑driven pharmaceutical company.
• Professional development and training in quality systems.
• Collaborative environment aligned with Recordati’s values.